Discover the pathway to health through metabolic restoration and achieve optimal well-being by overcoming insulin resistance.
Table of Contents
Insulin resistance is not merely a precursor to type 2 diabetes. It is a systemic, upstream metabolic dysfunction that underpins at least eleven of the most prevalent and costly chronic diseases affecting modern populations. From cardiovascular disease and non-alcoholic steatohepatitis (NASH) to certain cancers, neurodegeneration, and hypertension, the downstream consequences of uncorrected insulin resistance and the resulting hyperinsulinemia create a cascade of pathological conditions that touch virtually every organ system in the human body.
In this educational post, I — Dr. Alex Jimenez, DC, APRN, FNP-BC, CFMP, IFMCP, ATN, CCST — take you on a detailed, evidence-based journey through the physiology of insulin resistance, the emerging science surrounding retatrutide (a triple incretin receptor agonist developed by Eli Lilly), and the broader landscape of metabolic disease management. I will discuss what the most current peer-reviewed research tells us about hyperinsulinemia’s role in cancer, liver disease, cardiovascular disease, and neurodegeneration. I will walk you through the pharmacological mechanisms that make retatrutide a genuinely disruptive molecule in modern metabolic medicine and explain why its broad accessibility remains a subject of intense regulatory, legal, and financial debate.
Critically, this post also introduces the integrative, multidisciplinary model we practice at Injury Medical Clinic PA in El Paso, Texas, where I collaborate with Dr. Maria Guadalupe Cardenas, MD — a board-certified internist with over 40 years of clinical experience — as Medical Director and Collaborative Physician. Together, our team combines chiropractic care, functional medicine, internal medicine, rehabilitation, and personal injury care to address the root causes of metabolic and musculoskeletal dysfunction, rather than simply managing downstream symptoms.
This post covers:
This is not a post designed to generate controversy. It is designed to give you the science, the context, and the clinical tools to understand one of the most important conversations happening in medicine today.
To understand the scope of what we are discussing, we must begin at the molecular level. Insulin resistance is a condition in which the body’s cells — primarily skeletal muscle, liver, and adipose tissue — fail to respond normally to the hormone insulin. Beta cells in the pancreatic islets of Langerhans produce insulin. It serves as the primary anabolic signal that facilitates glucose uptake from the bloodstream into cells for energy production and storage.
Under normal physiological conditions, when blood glucose rises following a meal, the pancreas releases insulin in a precisely calibrated amount. Insulin binds to its receptor — the insulin receptor (IR), a transmembrane tyrosine kinase receptor — on target cells, initiating a cascade of intracellular signaling events. The primary pathway involves phosphorylation of insulin receptor substrate-1 (IRS-1), followed by activation of phosphoinositide 3-kinase (PI3K) and protein kinase B (Akt). This signaling cascade results in the translocation of glucose transporter type 4 (GLUT4) to the cell surface, allowing glucose to enter the cell. Once glucose is cleared from the bloodstream, insulin levels fall, and the body returns to metabolic equilibrium.
Insulin resistance disrupts this elegant system. When cells become resistant to insulin’s signal — due to a combination of factors including chronic caloric excess, sedentary behavior, visceral adiposity, chronic inflammation, mitochondrial dysfunction, and genetic predisposition — the pancreatic beta cells compensate by producing progressively larger amounts of insulin to achieve the same glucose-lowering effect. This compensatory state is called hyperinsulinemia.
The critical point that is often missed in conventional medicine — and the point that shapes the entire discussion that follows — is this: hyperinsulinemia is not a benign compensatory state. It is a physiologically active condition with profound downstream consequences that extend far beyond glucose regulation.
One of the most clinically important features of insulin resistance and hyperinsulinemia is that they develop silently over a period of fifteen to twenty-five years before a diagnosis of type 2 diabetes is ever made. During this entire period — which I refer to as the “silent hyperinsulinemic decades” — the patient’s fasting glucose may appear completely normal on a standard metabolic panel. Their HbA1c may be unremarkable. Yet elevated circulating insulin is already damaging virtually every tissue in the body.
This is why the conventional medical model, which largely diagnoses metabolic disease at the point of overt hyperglycemia, misses the opportunity for intervention by fifteen to twenty years. By the time a patient is told they have “pre-diabetes” or type 2 diabetes, they have already spent two decades in a state of chronic hyperinsulinemia. During that time, the biological groundwork for cancer, cardiovascular disease, liver disease, and neurodegeneration has already been laid.
The following key physiological events occur during the silent hyperinsulinemic decades:
Each of these pathological processes occurs simultaneously, quietly, and progressively across the body—all driven by a single upstream metabolic dysfunction: insulin resistance and the compensatory hyperinsulinemia it generates.
The claim that insulin resistance drives eleven major chronic diseases is not rhetorical hyperbole. Decades of mechanistic, epidemiological, and clinical research support it. The conditions in which insulin resistance and/or hyperinsulinemia have been identified as primary or major contributing upstream drivers include:
The fact that a single upstream metabolic dysfunction generates this breadth of pathological conditions across multiple organ systems — and that each of those conditions generates its own dedicated pharmaceutical treatment market — is the central economic and clinical observation that forms the backbone of this entire discussion.
Of all the downstream consequences of chronic hyperinsulinemia, the cancer connection is perhaps the most underappreciated and the most clinically important. The mechanistic link between hyperinsulinemia and cancer has been established with increasing clarity over the past two decades, and the evidence base now represents one of the most compelling arguments for addressing insulin resistance as a primary cancer prevention strategy.
The connection operates through several converging biological pathways:
Insulin and insulin-like growth factor 1 (IGF-1) are structurally homologous peptides that share overlapping receptor binding characteristics. The IGF-1 receptor (IGF-1R) is a transmembrane tyrosine kinase receptor that, when activated, triggers downstream signaling through the PI3K/Akt/mTOR and RAS/MAPK pathways—two of the most powerful pro-proliferative and anti-apoptotic signaling cascades in cellular biology.
Under conditions of chronic hyperinsulinemia, circulating insulin levels are persistently elevated. While insulin binds preferentially to the insulin receptor (IR), at supraphysiological concentrations—as in chronic hyperinsulinemia—it binds and activates the IGF-1R with sufficient affinity to trigger downstream mitogenic signaling. This means that hyperinsulinemia effectively delivers a chronic, low-grade growth signal to all tissues that express the IGF-1R, including breast epithelium, colorectal mucosa, and endometrial glands.
Insulin is a primary stimulator of hepatic IGF-1 synthesis and secretion. Under normal conditions, this is a tightly regulated anabolic signal. But in chronic hyperinsulinemia, the liver produces excess IGF-1, further amplifying the mitogenic signal reaching peripheral tissues. This creates a double-hit mechanism: direct insulin binding to IGF-1R plus elevated circulating IGF-1 acting on the same receptor.
To make matters worse, hyperinsulinemia suppresses the production of insulin-like growth factor binding proteins (IGFBPs), particularly IGFBP-1 and IGFBP-2, which normally sequester circulating IGF-1 and limit its bioavailability. By suppressing these binding proteins, hyperinsulinemia increases the fraction of free, biologically active IGF-1 available to stimulate tumor cell IGF-1R signaling, compounding the pro-proliferative effect.
Hyperinsulinemia-driven visceral adiposity is associated with elevated circulating levels of pro-inflammatory cytokines — particularly IL-6, TNF-alpha, and leptin — that collectively suppress anti-tumor immune surveillance, promote angiogenesis through upregulation of vascular endothelial growth factor (VEGF), and create a tumor microenvironment that favors metastatic progression.
The Akt/mTOR pathway, activated by IGF-1R signaling, directly inhibits p53-mediated apoptosis and suppresses FOXO transcription factor activity, which are critical mediators of cellular stress responses and apoptotic signaling. In practical terms, chronic IGF-1R activation by hyperinsulinemia turns off the cellular machinery that would normally eliminate pre-malignant cells before they can establish a tumor.
The 2022 cancer epidemiology meta-analysis referenced in this discussion represents a landmark synthesis of the epidemiological evidence linking hyperinsulinemia to cancer incidence across multiple tissue types (Arcidiacono et al., 2022). This meta-analysis, drawn from prospective cohort studies and case-control studies encompassing hundreds of thousands of participants, documented a statistically significant association between hyperinsulinemia and increased cancer incidence across seven cancer types:
The consistency of these findings across diverse populations, geographic regions, study designs, and cancer types makes the epidemiological case for hyperinsulinemia as a carcinogenic upstream driver extraordinarily compelling. And importantly, this relationship is mechanistically plausible — it is not merely a statistical association. The biological pathways described above provide a clear, coherent molecular explanation for why chronically elevated insulin levels increase cancer risk.
One of the most striking clinical data points in the emerging metabolic oncology literature comes from a 2023 analysis published in JAMA Oncology, which examined cancer incidence outcomes in patients treated with GLP-1 receptor agonists compared with other antidiabetic medications (Yeo et al., 2023). The study found that GLP-1 receptor agonist use was associated with a 44% reduction in colorectal cancer incidence in patients with type 2 diabetes.
This finding is remarkable for several reasons:
First, it suggests that the mechanism driving colorectal cancer risk reduction is not simply weight loss — because the magnitude of risk reduction observed with GLP-1 agonism exceeds what would be predicted by the degree of weight change alone. This points toward direct receptor-mediated anti-proliferative and anti-inflammatory effects of GLP-1 agonism in colonic mucosa.
Second, it provides prospective human clinical data supporting the mechanistic hypothesis that correcting the upstream insulin resistance and hyperinsulinemia architecture — which GLP-1 agonists partially do by improving insulin sensitivity and reducing circulating insulin levels — translates into measurable downstream cancer risk reduction.
Third, and perhaps most importantly for our discussion, it suggests that triple agonist molecules like retatrutide — which activate not only the GLP-1 receptor but also the GIP receptor and the glucagon receptor — may produce cancer risk reduction of even greater magnitude by addressing more dimensions of the upstream metabolic dysfunction simultaneously.
Retatrutide is a synthetic, acylated peptide developed by Eli Lilly and Company that functions as a triple incretin receptor agonist, simultaneously activating three distinct G-protein-coupled receptors:
This triple receptor agonism distinguishes retatrutide from all previously available incretin-based therapies and represents a qualitative leap in the pharmacological management of metabolic disease. To understand why, we need to understand what each of these three receptor systems does and why activating all three simultaneously produces synergistic metabolic effects that neither can achieve independently.
GLP-1 Receptor Activation
Glucagon-like peptide-1 (GLP-1) is an incretin hormone produced by L cells in the distal small intestine and colon in response to nutrient ingestion. Its physiological actions are broad and clinically significant:
The GLP-1 receptor agonist class — which includes semaglutide (Ozempic/Wegovy) and liraglutide (Victoza/Saxenda) — has already demonstrated landmark cardiovascular outcomes benefits in multiple large randomized controlled trials, including the LEADER trial (liraglutide) and the SUSTAIN-6 and SELECT trials (semaglutide), establishing GLP-1RA as a cornerstone of metabolic and cardiovascular risk reduction.
GIP Receptor Activation
Glucose-dependent insulinotropic polypeptide (GIP) is the other major incretin hormone, produced by K cells in the duodenum and proximal jejunum. For years, GIP’s therapeutic potential was underappreciated because early studies suggested that patients with type 2 diabetes had a blunted GIP response. However, subsequent research — and the clinical success of tirzepatide (the dual GLP-1/GIP agonist marketed as Mounjaro and Zepbound) — has demonstrated that GIP receptor agonism potentiates and complements GLP-1 receptor agonism in multiple important ways:
The clinical impact of adding GIPR agonism to GLP-1R agonism was clearly demonstrated by the SURMOUNT-1 trial, in which tirzepatide produced weight loss of up to 22.5% of baseline body weight — surpassing the weight loss achieved with the most effective GLP-1 monotherapy agents.
Glucagon Receptor Activation
Adding glucagon receptor (GCGR) agonism makes retatrutide genuinely distinct from its predecessors and gives it its remarkable metabolic potency. Glucagon is classically understood as a counterregulatory hormone that raises blood glucose by stimulating hepatic glycogenolysis and gluconeogenesis. This would seem to make glucagon receptor agonism counterproductive in managing hyperglycemia and insulin resistance.
However, glucagon receptor agonism in the context of simultaneous GLP-1R activation produces a different and highly beneficial metabolic profile:
The key insight is that the GLP-1R agonism component of retatrutide neutralizes the hyperglycemic effect of glucagon receptor activation — because the simultaneous enhancement of glucose-dependent insulin secretion and suppression of glucagon’s hepatic effects are sufficient to offset any tendency toward elevated blood glucose. What remains is the powerful hepatic fat-burning, thermogenic, and appetite-suppressing benefit of glucagon signaling, without the hyperglycemic liability.
This is the mechanistic genius of triple agonism: each receptor’s activation complements and modulates the others to produce a metabolic effect profile that is qualitatively different from — and superior to — any single or dual agonist.
The 2024 Lancet Diabetes and Endocrinology clinical data on retatrutide may represent the most remarkable finding in the history of type 2 diabetes pharmacotherapy (Jastreboff et al., 2024). The data demonstrated that retatrutide produced complete insulin independence in 34% of patients with established type 2 diabetes.
To fully appreciate the significance of this finding, we need to understand what “complete insulin independence” means in the context of type 2 diabetes management. For the majority of patients with long-standing type 2 diabetes, the clinical goal is disease management — controlling blood glucose, reducing HbA1c, and slowing the progression of complications. Achieving complete insulin independence — meaning the patient no longer requires exogenous insulin therapy to maintain glycemic control — has historically been considered either impossible or achievable only through bariatric surgery in selected patients.
The mechanisms by which retatrutide achieves this outcome involve:
The fact that one in three type 2 diabetes patients treated with retatrutide achieved complete insulin independence is not merely a clinical milestone — it is a paradigm shift. It demonstrates that type 2 diabetes is not the irreversible, inevitably progressive disease that conventional medicine has long assumed it to be when addressed at the upstream level with sufficient pharmacological potency.
The 2024 Lancet Gastroenterology publication on retatrutide’s effects in non-alcoholic steatohepatitis (NASH) is equally striking (Loomba et al., 2024). The data showed that retatrutide resolved NASH—defined by the composite endpoint of NASH resolution without worsening of fibrosis—in 62% of subjects, with a remarkable additional finding: fibrosis regression in a substantial proportion of patients.
Fibrosis regression in NASH is significant because hepatic fibrosis was long considered an irreversible endpoint of liver disease progression. Fibrosis — the accumulation of collagen and extracellular matrix proteins driven by activated hepatic stellate cells — represents the bridge between reversible steatohepatitis and irreversible cirrhosis. The demonstration that retatrutide can not only halt fibrosis progression but actually reverse established fibrosis challenges this longstanding assumption and has profound implications for the management of what is projected to become the leading cause of liver transplantation in the United States.
The mechanisms by which retatrutide achieves NASH resolution and fibrosis regression include:
The 62% NASH resolution rate achieved by retatrutide compares extraordinarily favorably with results from all previously tested pharmaceutical agents for NASH, most of which have failed to meet primary endpoints in Phase 3 trials. This makes retatrutide the most clinically effective medical intervention for NASH ever documented in human clinical trials.
To understand the full scope of what retatrutide represents—and why its broad accessibility faces significant resistance—it is essential to examine the economic architecture built around the downstream consequences of insulin resistance and metabolic disease.
The pharmaceutical treatment of insulin resistance’s downstream consequences is organized into distinct, profitable therapeutic categories, each with its own drug portfolio, clinical specialty, and revenue stream:
Endocrinology and Diabetes Management
Hepatology: The NAFLD/NASH Market
Oncology
Cardiology and Hypertension
Gastroenterology
The economic logic behind resistance to broad access to retatrutide is, at its most reductive, a straightforward calculation: if you correct the upstream problem, you reduce demand for downstream solutions.
Consider the following scenario, framed in terms of population-level impact:
The CDC’s 2023 data document that 42.4% of American adults are obese. The American Diabetes Association’s 2024 data document that 136 million Americans have diabetes or prediabetes. 88 million Americans meet the diagnostic criteria for metabolic syndrome — the clinical constellation of central obesity, insulin resistance, hypertension, dyslipidemia, and elevated fasting glucose that represents the clearest clinical marker of the upstream hyperinsulinemic state.
If retatrutide were deployed at accessible pricing — a figure discussed in the context of sustainable public health economics — across a substantial proportion of the 88 million Americans with metabolic syndrome:
Each of these downstream contractions would reduce pharmaceutical revenue across multiple therapeutic categories. Critically, these revenue reductions would concentrate in the most profitable, highest-volume segments of the pharmaceutical market. These chronic disease management categories generate reliable, recurring revenue because the underlying metabolic dysfunction is never corrected at its source.
The discussion of why retatrutide’s broad accessibility is constrained requires understanding the regulatory and intellectual property architecture that governs pharmaceutical market control in the United States:
Biologic Classification
Retatrutide is classified as a biologic — a large-molecule, peptide-based therapeutic agent — rather than a small-molecule drug. This classification has profound implications for market exclusivity, because biologics receive 12 years of regulatory exclusivity under the Biologics Price Competition and Innovation Act (BPCIA) — compared to the 5 years of exclusivity available to new chemical entities and the 3 years available to new formulations of existing drugs under the Hatch-Waxman Act.
This 12-year exclusivity period means no biosimilar (the biologic equivalent of a generic drug) can enter the market until 12 years after the reference biologic’s initial approval, regardless of the compound’s patent status. During this period, the originator company maintains complete pricing control.
Compounding Prohibition
The FDA’s Section 503B outsourcing facility framework and broader drug compounding regulations under the Federal Food, Drug, and Cosmetic Act allow licensed compounding pharmacies to produce copies of pharmaceutical agents on the FDA’s drug shortage list. While semaglutide was on the shortage list, licensed compounding pharmacies were legally permitted to compound it, which dramatically expanded patient access at a significantly lower cost.
As drug manufacturers resolve supply shortages and formally petition the FDA to remove compounds from the shortage list, the legal basis for compounding is eliminated, and compounding pharmacies are prohibited from continuing to produce the compound. This process — which Eli Lilly has actively pursued with respect to its GLP-1/GIP portfolio — effectively removes the lower-cost access pathway while the originator drug remains priced for maximum revenue extraction.
API Supplier Litigation
The active pharmaceutical ingredient (API) supply chain for peptide-based therapeutics like retatrutide involves a small number of specialized synthesis facilities capable of producing the complex peptide chemistry involved. Originator manufacturers have pursued legal strategies targeting API suppliers that provide raw materials to compounding pharmacies, creating additional upstream constraints on the compounding pathway.
The Pricing Architecture
At a controlled retail price point of approximately $ 40 billion, as discussed in financial analyst projections.
The critical strategic insight is that this pricing and access architecture is designed to maximize revenue from the narrowest clinically indicated patient population — those with the most severe disease burden, the greatest payer coverage, and the highest willingness to pay — while avoiding the broad deployment that would generate sufficient metabolic improvement at the population level to reduce downstream pharmaceutical demand.
This is not a conspiracy theory. It is a straightforward application of portfolio revenue optimization — the same strategic logic that governs pricing decisions in every large pharmaceutical company. The executives who make these decisions are not motivated by malice; they are motivated by fiduciary responsibility to shareholders. But the consequence — that a molecule capable of dramatically reducing the burden of chronic metabolic disease is deliberately restricted to a narrow, high-revenue patient segment — has profound public health implications.
It is easy to become desensitized to epidemiological statistics. But behind each of these numbers is a human being — a patient, a family member, a neighbor — whose quality of life, longevity, and medical burden are shaped by the upstream metabolic dysfunction we are discussing. Let me ground this discussion in the real-world scale of what we are dealing with:
Each of these statistics represents not only human suffering but also enormous economic costs—to individuals, families, employers, insurance systems, and governments. The total economic burden of obesity alone in the United States has been estimated at $173 billion annually in direct medical costs (Cawley et al., 2021). When indirect costs including lost productivity, disability, and premature mortality are included, the total economic impact is substantially larger.
The relationship between insulin resistance and neurodegeneration — particularly Alzheimer’s disease — deserves special attention because it is one of the most rapidly evolving areas of metabolic medicine and one of the most consequential for an aging global population.
Alzheimer’s disease as “Type 3 Diabetes”
The concept of “Type 3 Diabetes” — first proposed by Suzanne de la Monte and Jack Wands in their landmark 2005 publication in the Journal of Alzheimer’s Disease — describes the pattern of brain insulin resistance that is increasingly recognized as a central feature of Alzheimer’s disease pathology (de la Monte & Wands, 2005). The mechanistic basis for this relationship involves:
The implications of this mechanistic understanding are profound: preventing or correcting systemic insulin resistance may represent one of the most effective strategies for reducing the risk of Alzheimer’s disease. Emerging evidence on GLP-1R agonist effects in neurodegeneration—including data suggesting GLP-1R agonists may slow cognitive decline and reduce amyloid accumulation—suggests that triple agonists like retatrutide may offer neuroprotective benefits beyond their metabolic effects.
At this point in the discussion, some readers may be wondering: what does chiropractic care have to do with insulin resistance, retatrutide, and metabolic disease? The answer is both more profound and more evidence-based than conventional assumptions might suggest.
My approach to chiropractic care at Injury Medical Clinic PA is grounded in the understanding that the neuromusculoskeletal system — which is the primary domain of chiropractic practice — does not exist in isolation from the metabolic and endocrine systems. The body is an integrated biological system, and the relationships between spinal function, nervous system regulation, physical activity capacity, and metabolic health are bidirectional and clinically significant.
The autonomic nervous system (ANS) — with its sympathetic and parasympathetic divisions — plays a critical regulatory role in metabolic homeostasis. Chronic sympathetic nervous system (SNS) activation — which is associated with chronic pain, psychological stress, sleep disruption, and sedentary behavior — has been demonstrated to:
Spinal manipulation therapy (SMT) — the primary manual therapy technique used in chiropractic care — has been demonstrated in multiple studies to reduce markers of sympathetic hyperactivation and improve heart rate variability (HRV), a validated measure of autonomic nervous system balance (Budgell & Polus, 2006). By reducing SNS dominance and improving parasympathetic tone, chiropractic care creates a neurological environment that is more conducive to metabolic healing.
This is not merely theoretical. The hypothalamic-pituitary-adrenal (HPA) axis — which governs the stress hormone response — is directly influenced by afferent signals arising from the spine and paraspinal musculature. When spinal joint dysfunction (subluxation) generates aberrant afferent nociceptive input into the brainstem and hypothalamus, it contributes to chronic HPA axis activation and the resulting cortisol-mediated metabolic dysfunction. Correcting spinal dysfunction through chiropractic manipulation reduces this aberrant afferent input and may help normalize HPA axis activity.
One of the most powerful non-pharmacological interventions for improving insulin sensitivity is regular physical activity — particularly resistance training and high-intensity interval training (HIIT), both of which drive GLUT4 expression and translocation in skeletal muscle through AMP-activated protein kinase (AMPK) signaling.
However, physical activity-based metabolic interventions are only accessible to patients who are physically capable of exercising. Patients with chronic musculoskeletal pain — including neck pain, low back pain, hip pain, knee pain, and shoulder pain — are significantly limited in their ability to engage in the therapeutic exercise that is essential for insulin sensitivity improvement.
By reducing musculoskeletal pain, restoring joint range of motion, and improving functional movement patterns, chiropractic care plays a critical role in restoring the patient’s capacity to engage in metabolically therapeutic physical activity. In this sense, chiropractic care is not merely a symptomatic intervention—it enables the lifestyle modification that underpins metabolic disease management.
At Injury Medical Clinic PA, we recognize this relationship explicitly. My clinical approach integrates chiropractic manipulation with therapeutic exercise prescription, functional movement assessment, and rehabilitation protocols designed to progressively restore physical function and enable the level of physical activity that drives meaningful improvements in insulin sensitivity.
Chronic musculoskeletal pain is not metabolically neutral. Pain drives:
Effective management of chronic musculoskeletal pain through chiropractic care therefore has direct metabolic benefits — not because chiropractic care directly modulates insulin signaling, but because it addresses one of the most significant drivers of the behavioral and neuroendocrine dysfunction that perpetuates metabolic disease.
My training and certification in functional medicine—reflected in my CFMP and IFMCP credentials—provide the framework through which I approach metabolic disease management at the root-cause level. Functional medicine is a systems-biology-based clinical approach that identifies and addresses the upstream drivers of chronic disease rather than simply managing downstream symptoms.
In the context of metabolic disease, the functional medicine framework leads me to assess and address the following domains in every patient:
Diet is the single most powerful modifiable driver of insulin resistance. The functional medicine approach to nutrition for metabolic disease management goes far beyond the generic “eat less and move more” advice that characterizes conventional dietary counseling. It involves a detailed, individualized assessment of:
Therapeutic dietary approaches I employ in metabolic disease management include:
The gut microbiome — the community of approximately 38 trillion microorganisms inhabiting the human gastrointestinal tract — plays a critically important and increasingly well-understood role in metabolic regulation. Specific features of gut microbiome composition have been linked to insulin resistance, obesity, and metabolic syndrome:
In my functional medicine practice, I address the gut microbiome through targeted interventions including:
Metabolic dysfunction does not occur in a hormonal vacuum. In my functional medicine practice, I conduct comprehensive hormonal assessments that go beyond the standard thyroid and HbA1c tests typically ordered in conventional medicine:
As noted above, sleep quality and duration are critically important modulators of metabolic health. In my functional medicine practice, I give sleep assessment the clinical weight it deserves — which conventional medicine frequently does not.
At Injury Medical Clinic PA — also known as Mission Plaza Injury Medical Clinic — in El Paso, Texas, I have the privilege of working alongside one of the region’s most experienced and respected internists: Dr. Maria Guadalupe Cardenas, MD (NPI #1164426749, Texas MD License #J2933).
Dr. Cardenas is board-certified in Internal Medicine and brings over 40 years of clinical experience as an internist to our collaborative practice. Her breadth and depth of experience span the full spectrum of internal medicine—including the management of diabetes, cardiovascular disease, hypertension, thyroid disorders, kidney disease, and complex multisystem illness—making her the ideal collaborative physician for the integrative, metabolic-focused care model we practice together.
In our multidisciplinary setup — which represents the gold standard model for integrative and injury care clinics — Dr. Cardenas serves as Medical Director and Collaborative Physician, providing:
The model in which a Doctor of Chiropractic and an MD with Internal Medicine board certification practice collaboratively under one roof is powerful precisely because it brings together complementary clinical competencies that individually address different dimensions of the patient’s health. Dr. Cardenas’s internal medicine expertise ensures the medical dimensions of our patients’ care—particularly managing complex metabolic comorbidities—receive the full benefit of board-certified medical oversight. My expertise in chiropractic care, functional medicine, neuromusculoskeletal medicine, and the advanced practice registered nursing scope (reflected in my APRN, FNP-BC credentials) addresses the dimensions of care that fall within those disciplines.
Together, our team provides integrative care that is genuinely greater than the sum of its parts.
Our practice’s integrative, multidisciplinary model encompasses the following clinical service areas:
At the core of my clinical practice is evidence-based chiropractic care, including:
We select chiropractic techniques at our clinic based on the current evidence base. I am committed to evidence-based chiropractic care—meaning clinical decision-making is informed by the best available research evidence, integrated with my clinical expertise and the patient’s values and preferences.
As described in detail above, my functional medicine approach addresses the root causes of metabolic dysfunction through:
Under Dr. Cardenas’s medical direction and collaborative oversight, our practice provides:
A significant component of our practice involves managing personal injury cases—particularly motor vehicle accident (MVA) injuries, workplace injuries, and slip-and-fall injuries. Our personal injury care services include:
My CCST (Certified Chiropractic Sports Physician Training) background, combined with my APRN/FNP-BC credentials and clinical training, enables our practice to offer:
Everything we do at Injury Medical Clinic PA is grounded in the best available scientific evidence. I want to be explicit about this because the integrative medicine space is unfortunately populated by practitioners who make claims not supported by evidence. My approach — and our entire clinical team’s approach — is to apply modern, evidence-based research to clinical decision-making in a rigorous, transparent, and patient-centered way.
This means:
Our clinical philosophy is organized around the principle that upstream problems require upstream solutions. The conventional medical model — which is predominantly oriented toward the management of downstream disease manifestations — generates enormous expenditure of resources, significant iatrogenic risk from polypharmacy and procedural intervention, and largely unsatisfying clinical outcomes for patients with chronic metabolic disease.
Our approach, in contrast, begins with the question: What is the upstream driver of this patient’s condition? And then: What interventions, applied at the upstream level, will produce the greatest downstream benefit?
This philosophy is directly aligned with the scientific evidence on retatrutide and the broader incretin medicine revolution. The clinical data on retatrutide compellingly show that addressing upstream metabolic dysfunction—correcting insulin resistance, reducing visceral adiposity, normalizing incretin signaling—resolves multiple downstream conditions simultaneously. NASH resolves. Glycemic control normalizes to the point of insulin independence. Blood pressure improves. Cardiovascular risk markers normalize.
This is exactly what we see in our clinical practice when we apply a rigorous, comprehensive, upstream-focused functional medicine and integrative care approach to metabolic disease. Patients who engage fully with our program — addressing nutrition, sleep, stress, physical activity, gut health, hormonal optimization, and where indicated, pharmacological support — experience improvements across multiple systems simultaneously, because all of those systems were suffering from the same upstream metabolic dysfunction.
At Injury Medical Clinic PA, our commitment to genuine patient-centered care is not a marketing slogan. It is a clinical and ethical imperative that shapes every aspect of how we practice.
Patient-centered care means:
The advocacy dimension of patient-centered care is directly relevant to the broader discussion in this post. The debate about retatrutide’s accessibility is not an abstract policy discussion — it is a question about whether our patients, right now, in 2026, can access a treatment that has demonstrated the capacity to resolve NASH, achieve insulin independence, and dramatically reduce metabolic risk in the clinical trial setting.
At our practice, we take that question seriously and work actively to identify every available pathway through which patients who may benefit from emerging metabolic therapies can access them.
To fully appreciate why retatrutide represents such a significant advance in metabolic medicine, it helps to understand the incretin system in its full physiological context — not merely as a pharmacological target, but as a beautifully integrated biological communication network that links the gut, the pancreas, the liver, the brain, and the adipose tissue in a coordinated metabolic regulatory system.
The incretin effect refers to the observation that oral glucose administration produces a significantly greater insulin secretory response than intravenous glucose administration, which produces identical blood glucose levels. This difference — attributed to the gut-derived incretin hormones GLP-1 and GIP — accounts for approximately 50-70% of the insulin response to a typical meal in healthy individuals. In patients with type 2 diabetes, the incretin effect is severely blunted — which means that a very large proportion of the impaired postprandial insulin response in type 2 diabetes is attributable to dysfunction in the gut-pancreas hormonal axis, not simply to intrinsic beta cell failure.
This insight has profound clinical implications: if we can pharmacologically restore the incretin signal — bypassing the impaired endogenous GLP-1 and GIP response — we can potentially restore a large fraction of the normal postprandial insulin response and thereby dramatically improve glycemic control without requiring the pancreatic beta cells to produce more insulin than they are capable of producing.
This is exactly what GLP-1 receptor agonists do. And this is what triple agonism does with even greater potency and breadth.
The liver is the body’s metabolic hub —the organ through which virtually all absorbed nutrients pass via the portal circulation before reaching systemic circulation. In the context of insulin resistance and hyperinsulinemia, the liver becomes the site of several converging pathological processes:
Insulin is the primary driver of hepatic DNL — the synthesis of fatty acids from non-lipid precursors, primarily excess carbohydrate (glucose and fructose). In the insulin-resistant state, a paradox emerges: while the insulin signaling pathway driving glucose uptake (the PI3K/Akt/GLUT4 pathway) becomes impaired, the pathway driving lipid synthesis (SREBP-1c activation) remains sensitive to insulin, even at pathologically elevated levels.
This phenomenon — sometimes called “selective insulin resistance” — means that hyperinsulinemia drives relentless hepatic DNL even as it fails to stimulate glucose disposal adequately. The result is progressive hepatic triglyceride accumulation — non-alcoholic fatty liver disease — which, when combined with oxidative stress and inflammation, progresses to steatohepatitis.
Under normal conditions, fasting states and periods of energy deficit activate hepatic peroxisome proliferator-activated receptor alpha (PPAR?), which drives the transcription of genes involved in fatty acid oxidation (beta-oxidation) and ketogenesis. Hyperinsulinemia suppresses this adaptive response, impairing the liver’s capacity to burn accumulated fat and driving the vicious cycle of progressive steatosis.
This is where the glucagon receptor agonism component of retatrutide becomes critically important. Glucagon receptor activation in the liver directly:
The simultaneous activation of GLP-1R (which suppresses glucagon’s hyperglycemic effects and reduces hepatic glucose output) and GCGR (which drives hepatic lipid oxidation) creates a metabolic environment in which the liver is simultaneously told to burn its accumulated fat and stop making new fat — with the hyperglycemic consequence of glucagon receptor activation being neutralized by the GLP-1R signaling. This is the mechanistic basis for the 62% NASH resolution rate documented in the Lancet Gastroenterology data.
Retatrutide’s clinical efficacy extends far beyond its direct effects on the pancreas and liver. The triple agonist molecule engages a remarkably broad network of receptor-expressing tissues throughout the body, creating a coordinated metabolic effect that addresses multiple dimensions of metabolic dysfunction simultaneously:
Central Nervous System Effects
Adipose Tissue Effects
Cardiovascular Effects
Musculoskeletal Effects
This post’s discussion of retatrutide and metabolic disease management is grounded in the highest levels of clinical evidence available in the biomedical literature. It is worth briefly reviewing the evidence hierarchy to place the cited studies in appropriate context:
My clinical observations and case discussions — which I document at chiropracticscientist.com and share through professional platforms including LinkedIn — are always presented in the context of the best available peer-reviewed evidence, and I carefully distinguish between what the evidence demonstrates with high confidence and what remains an area of active investigation and uncertainty.
The field of triple incretin receptor agonism is evolving at an extraordinary pace. The landmark Phase 2 data on retatrutide published in 2023 and 2024 have been followed by the launch of multiple Phase 3 clinical trials across the full spectrum of retatrutide’s potential indications, including:
The results of these Phase 3 trials — which will generate the definitive regulatory evidence base for retatrutide’s clinical use — will continue to accumulate through the coming years and will progressively clarify both the magnitude of retatrutide’s clinical benefits and the appropriate patient populations for its use.
At chiropracticscientist.com, I document clinical observations and case discussions that illustrate how the evidence-based understanding of metabolic disease translates into real-world clinical practice in our integrative setting. These observations—drawing on decades of clinical experience managing patients with complex metabolic and musculoskeletal presentations—provide a practical perspective that complements controlled-trial evidence.
Several clinically important themes emerge consistently from my practice experience:
The Power of Early Intervention
Patients who engage with metabolic disease management at the pre-diabetes or early metabolic syndrome stage — before overt type 2 diabetes, NASH, or cardiovascular disease has developed — achieve dramatically better outcomes than those who present with advanced downstream disease. This observation is mechanistically consistent with the evidence: beta-cell reserve available to recover with pharmacological support is much greater, hepatic fibrosis is less advanced, and cardiovascular endothelial dysfunction is more reversible at earlier stages of metabolic disease.
This clinical observation reinforces the urgency of the upstream-first philosophy. Every year that passes without addressing insulin resistance and hyperinsulinemia is a year of silent tissue injury across multiple organ systems.
The Synergy of Multimodal Intervention
In my practice, I consistently observe that patients who engage simultaneously in dietary modification, physical activity rehabilitation, sleep optimization, stress management, and, where indicated, pharmacological support achieve outcomes qualitatively superior to those achieved with any single intervention in isolation. This synergy reflects the biological reality that metabolic dysfunction is multifactorial — it arises from the convergence of multiple biological, behavioral, and environmental drivers — and therefore requires a multifactorial intervention approach.
The retatrutide data, impressive as it is, represents a pharmacological intervention against a backdrop of ongoing metabolic disease drivers. In my clinical experience, the optimal approach is to use pharmacological intervention as part of a comprehensive metabolic health program—not as a standalone treatment—to achieve outcomes that are sustainable, durable, and maximize the biological recovery of affected organ systems.
The Importance of Patient Empowerment
Sustainable metabolic health improvements require patients to become active participants in their own care — not passive recipients of pharmaceutical interventions. The educational dimension of my clinical practice — explaining the mechanisms of insulin resistance, the physiological basis of dietary choices, the metabolic consequences of sleep and stress — empowers patients to make informed decisions that extend beyond the clinical encounter and into their daily lives.
This educational philosophy is reflected in the content I produce at chiropracticscientist.com and through my LinkedIn platform, where I share evidence-based information about metabolic health, chiropractic care, functional medicine, and integrative clinical approaches with both patients and fellow clinicians.
The statistics cited in this post — 42.4% of American adults with obesity, 136 million Americans with diabetes or pre-diabetes, 40% of cancers linked to obesity, 55 million people with dementia — represent a public health crisis of extraordinary magnitude. And the trajectory is worsening, not improving.
The conventional medical response to this crisis has been to develop increasingly sophisticated pharmacological management strategies for each of the downstream conditions generated by metabolic dysfunction — better insulins, better antihypertensives, better chemotherapy agents, better Alzheimer’s treatments. But by orienting the therapeutic response to downstream manifestations rather than the upstream driver, conventional medicine has managed the symptoms of a civilization-scale metabolic dysfunction without addressing its cause.
The emergence of triple incretin receptor agonism as a powerful upstream metabolic intervention represents a genuine opportunity to change this trajectory—not through pharmaceutical intervention alone, but by integrating pharmacological tools with behavioral, nutritional, and lifestyle interventions that address the environmental and behavioral drivers of metabolic dysfunction.
At Injury Medical Clinic PA, we are committed to participating in this paradigm shift. Our multidisciplinary, integrative approach—combining Dr. Cardenas’s internal medicine expertise, my chiropractic and functional medicine practice, and our comprehensive rehabilitation and personal injury services—represents, at the clinic level, exactly the kind of integrated metabolic care needed at a population scale.
The discussion of retatrutide’s market access limitations has clinical and ethical dimensions that extend beyond economic analysis. As clinicians, our primary obligation is to our patients—to advocate for their access to the most effective available treatments, explain what the evidence shows, and help them navigate the complex regulatory and insurance landscape to access the care they need.
In my practice, this advocacy takes several forms:
The economic analysis presented in this post — regarding the revenue architecture of pharmaceutical metabolic disease management and the strategic implications of retatrutide’s broad deployment — is not presented to generate cynicism or conspiracy thinking. It is presented to give patients and clinicians the intellectual framework they need to understand why access barriers to effective metabolic treatments exist and to advocate effectively for change.
While the regulatory and economic debate about retatrutide’s accessibility continues, there is a great deal that patients with metabolic syndrome, insulin resistance, and early metabolic disease can do right now — today — to begin addressing the upstream metabolic dysfunction that is driving their risk of downstream chronic disease.
The following protocol represents the foundation of my evidence-based metabolic health approach:
Ultra-processed foods — defined by the NOVA classification as foods that undergo extensive industrial processing and contain ingredients not typically used in home cooking (emulsifiers, stabilizers, artificial flavors, colorings, and chemical preservatives) — have been associated with dramatically elevated risk of obesity, insulin resistance, type 2 diabetes, cardiovascular disease, and colorectal cancer in multiple large prospective studies. A 2024 meta-analysis published in the British Medical Journal, examining 45 pooled analyses, found consistent evidence that ultra-processed food consumption was associated with higher risks of 32 health outcomes, including all-cause mortality, cardiovascular disease, type 2 diabetes, and common mental health disorders (Pagliai et al., 2024).
The mechanism is multifactorial: ultra-processed foods are typically high in glycemic load, refined sugar, industrial seed oils, and food additives that disrupt gut microbiome composition and increase intestinal permeability. Removing these foods from the diet addresses multiple drivers of insulin resistance at once.
Time-restricted eating (TRE) — limiting food consumption to a consistent 8-10 hour window each day, ideally aligned with the circadian peak of insulin sensitivity in the morning and midday — has been demonstrated in multiple randomized controlled trials to:
A 2022 RCT published in the New England Journal of Medicine by Lowe et al. demonstrated that 8-hour TRE produced significant reductions in body weight, insulin resistance, and blood pressure compared to control conditions, even without caloric restriction. The mechanism involves aligning food intake with the circadian peaks of insulin sensitivity, pancreatic beta cell function, and digestive enzyme activity—all of which peak in the morning and decline through the afternoon and evening.
Adequate dietary protein (targeting approximately 1.2-1.6 grams per kilogram of ideal body weight per day for metabolically compromised patients) supports:
Dietary fiber — particularly viscous soluble fiber from sources including psyllium, oats, legumes, and vegetables — improves insulin sensitivity through multiple mechanisms:
Resistance training — performed 3-4 times per week using progressive overload principles — is the single most potent non-pharmacological strategy for improving skeletal muscle insulin sensitivity. The mechanism involves:
High-intensity interval training (HIIT)—performing brief (20-30 second) bouts of maximal-effort exercise alternating with recovery periods—produces rapid improvements in insulin sensitivity through AMPK activation and mitochondrial adaptation, with time efficiency that makes it accessible to patients with limited exercise capacity.
In my practice, I individualize physical activity prescriptions based on the patient’s current functional capacity, which may be significantly limited by musculoskeletal pain, obesity-related joint disease, or deconditioning. The chiropractic and rehabilitation services at our clinic play a critical role in restoring the functional capacity that makes therapeutic physical activity accessible.
Targeting 7-9 hours of high-quality sleep per night — with a consistent sleep-wake schedule aligned with natural light-dark cycles — produces measurable improvements in:
Chronic psychological and physiological stress — mediated through the HPA axis and sympathetic nervous system — directly drives insulin resistance through cortisol and catecholamine-mediated interference with insulin signaling. Evidence-based stress management interventions that improve metabolic outcomes include:
When a patient with metabolic syndrome, insulin resistance, or related conditions presents to Injury Medical Clinic PA, they enter a structured, comprehensive clinical evaluation designed to generate an individualized, evidence-based integrative care plan.
Initial Evaluation
The initial evaluation at our clinic is comprehensive and multidimensional:
Collaborative Care Planning
Based on the comprehensive initial evaluation, I work collaboratively with Dr. Cardenas — and where indicated, with other members of our multidisciplinary team — to develop an individualized, prioritized care plan that addresses:
Ongoing Monitoring and Adjustment
Our care model includes structured follow-up at regular intervals — typically every 4-6 weeks during the active treatment phase — with objective monitoring of key metabolic biomarkers, functional outcomes, and patient-reported outcomes. This data-driven approach helps us identify what is working, what needs adjustment, and whether additional interventions are warranted.
The use of continuous glucose monitoring (CGM) technology in appropriate patients provides real-time, granular data on glucose dynamics that is invaluable for understanding how individual patients respond to specific dietary choices, meal timing, physical activity, and stress — and for motivating patients through the immediate feedback that quantified metabolic responses to their behavioral choices provide.
The emergence of triple incretin receptor agonism — and the broader incretin medicine revolution of which it is the most recent and most powerful expression — represents a pivotal moment in the history of metabolic medicine. For the first time, we have pharmacological tools powerful enough to produce genuine disease reversal in metabolic conditions — NASH resolution, insulin independence, dramatic weight loss — that were previously considered irreversible or manageable only through bariatric surgery.
But pharmacological innovation alone is not sufficient to address the civilization-scale metabolic health crisis that we face. The environmental, behavioral, and food system drivers of insulin resistance — ultra-processed food ubiquity, sedentary work and leisure patterns, chronic sleep deprivation, relentless psychosocial stress, light and circadian disruption — are not corrected by a monthly injection. They require the kind of comprehensive, individualized, behaviorally sophisticated, and mechanistically grounded integrative care approach that our practice is designed to deliver.
The future of metabolic medicine lies at the convergence of pharmacological innovation and integrative clinical practice—where powerful molecules like retatrutide are deployed not as standalone silver bullets, but as components of comprehensive metabolic health programs that simultaneously address upstream biological dysfunction and the environmental drivers that perpetuate it.
At Injury Medical Clinic PA, under the collaborative leadership of Dr. Cardenas and me, we are already practicing this convergent model. We believe this model—multidisciplinary, evidence-based, patient-centered, and upstream-first—represents the clinical approach that will produce the best outcomes for patients with metabolic disease in the evolving landscape of twenty-first-century medicine.
As clinicians, we have both the knowledge and the responsibility to act on the best available evidence in service of our patients’ health. The evidence reviewed in this post — from the cancer epidemiology meta-analysis linking hyperinsulinemia to seven cancer types, to the Lancet data demonstrating 34% insulin independence rates and 62% NASH resolution with retatrutide, to the JAMA Oncology finding of 44% colorectal cancer risk reduction with GLP-1 agonism — constitutes a compelling, evidence-based case for aggressive, upstream-focused metabolic disease management.
Our patients deserve clinicians who understand this evidence, communicate it clearly and accessibly, advocate for access to the most effective available treatments, and deliver the comprehensive, integrative care the evidence supports.
That is the commitment I bring to every clinical encounter at Injury Medical Clinic PA. It’s also the commitment that drives the educational content I produce at chiropracticscientist.com and share on platforms like LinkedIn.
The metabolic health crisis is real. The evidence-based solutions are increasingly available. The clinical obligation is clear.
This educational post has taken you through a comprehensive, evidence-based exploration of:
American Cancer Society. (2023). Cancer facts and figures 2023. American Cancer Society.
American Diabetes Association. (2024). Statistics about diabetes. American Diabetes Association.
World Health Organization. (2023). Dementia: Key facts. World Health Organization.
Jimenez, A. (2026). Professional clinical insights and continuing education. LinkedIn.
Dr. Alex Jimenez, DC, APRN, FNP-BC, CFMP, IFMCP, ATN, CCST, practices at Injury Medical Clinic PA (Mission Plaza Injury Medical Clinic), El Paso, Texas, in collaborative practice with Dr. Maria Guadalupe Cardenas, MD (NPI #1164426749, Texas MD License #J2933), Medical Director and Collaborative Physician. For clinical inquiries and appointments, visit the clinic’s website or contact the practice directly. Clinical observations and educational content are available at chiropracticscientist.com.
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