It is without a doubt that any imbalance in the body has a direct relationship influencing other body systems. Similar to many aspects in biochemical pathways, there needs to be a distinct concentration of input to output. Too much or too little production derails metabolic pathways quickly. However, research is finding that methyl groups and homocysteine metabolism have a profound effect on health and disease when disrupted.Â
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Homocysteine is a natural byproduct of SAM reactions, including the ones involved in the epigenetic regulation of DNA silencing. When homocysteine levels become overly elevated we see chaotic effects regarding our health and disease state. Homocysteine is a sulfur-containing amino acid that we obtain through the metabolism of methionine. Methionine is activated via MAT to generate SAM. SAMe is found in all living cells where it is a methyl donor to over 100 reactions. Methyl groups that are created from SAM are further used in creatine, phosphatidylcholine, and neurotransmitters. SAM-derived methylation also exerts a regulatory role in gene expression.Â
The methylation process has been best known for its role in cardiovascular disease and in relation to the adverse effects of homocysteine. A study revealed that humans that possessed the MTHFR C677T polymorphism had reduced activity of enzymes, ultimately leading to increased cardiovascular disease.Â
For more information regarding this study, please visit:Â
“Homocysteine Imbalance: A Pathological Metabolic Markerâ€Â
Homocysteine also plays a critical role in the soundness of our skeletal structure. Homocysteine has been shown to interfere with the activity of osteoclasts. Osteoclasts absorb bone tissue during routine growth and healing. When homocysteine is increased in the body, it up-regulates osteoclasts and depresses osteoclast apoptosis by increasing our overall reactive oxygen species in our bone marrow cells.Â
Additionally, homocysteine has been linked to neurodegenerative disorders. A specific disorder found to be related is depression. Depression has been defined as having low or impaired transmission of the neurotransmitters serotonin, dopamine, and norepinephrine. We now know that majority of the body’s serotonin is produced and housed in the gastrointestinal tract. When considering the tricky biochemical pathways of homocysteine and depression, the first thing considered should be the diet. Considering the micronutrients we feed our bodies are responsible for the smooth operations of our metabolic pathways we need to first evaluate if we are obtaining all proper nutrients. Secondly, when considering diet we need to ensure the foods that feed our cells and micronutrients are also foods that help the gut to thrive. The bacteria in the gut should be equally balanced for proper serotonin levels to be created and transported. Reducing inflammation in the gut will not only aid in serotonin production but in the reduction of homocysteine as well.Â
In order to properly check the bacteria levels in the gut, we use a comprehensive stool analysis from Doctors Data. Furthermore, we also check the micronutrient levels of our patients with a test from SpectraCell. A sample of both these reports can be seen below:
If homocysteine is not regulated properly a genetic error in our body can occur. This error occurs in the MTHFR gene. Generally, we have two MTHFR genes, we inherit one from each parent. If you have an SNP of the gene MTHFR, specifically C677T, this can result in an inadequate folate-dependent remethylation and elevations in homocysteine concentrations.Â
For those with an MTHFR mutation, many find that avoiding milk helps them feel better as many dairy antigens clog folate receptors. However, eating large amounts of leafy greens has been shown to help those with MTHFR as they help to compensate for the methylfolate not being made on its own.
For specific patients, B12, folate, and SAM supplements have been shown to reduce the homocysteine levels found in plasma and ultimately slow the progression and symptoms related to the abundance of homocysteine.Â
It is always best to provide our bodies and our genes with whole foods that we can break down easier for optimal gene expression. In supplements, you are not always getting the same amount of essential vitamins and minerals nor the full effect. Dietary guidelines suggest earring more fruits and vegetables to naturally lower homocysteine levels.Â
For more information regarding how MTHFR and nutrition are related, see the PDF below:Â
Starting in the kitchen, by making a quick smoothie in the morning containing dark leafy greens like spinach, flax seeds, strawberries, bananas, and almond milk, you are not only filling your stomach but also providing your body and gut with the essential micronutrients it needs to carry out its biochemical pathways. –Kenna Vaughn, Senior Health CoachÂ
References:Â
Schalinske KL, Smazal AL. Homocysteine imbalance: a pathological metabolic marker. Adv Nutr. 2012;3(6):755â€762. Published 2012 Nov 1. doi:10.3945/an.112.002758Â
The scope of our information is limited to chiropractic, musculoskeletal, and nervous health issues or functional medicine articles, topics, and discussions. We use functional health protocols to treat injuries or disorders of the musculoskeletal system. Our office has made a reasonable attempt to provide supportive citations and has identified the relevant research study or studies supporting our posts. We also make copies of supporting research studies available to the board and or the public upon request. To further discuss the subject matter above, please feel free to ask Dr. Alex Jimenez or contact us at 915-850-0900. Â
Professional Scope of Practice *
The information herein on "Homocysteine & Its Heavy Impact" is not intended to replace a one-on-one relationship with a qualified health care professional or licensed physician and is not medical advice. We encourage you to make healthcare decisions based on your research and partnership with a qualified healthcare professional.
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Our information scope is limited to Chiropractic, musculoskeletal, physical medicines, wellness, contributing etiological viscerosomatic disturbances within clinical presentations, associated somatovisceral reflex clinical dynamics, subluxation complexes, sensitive health issues, and/or functional medicine articles, topics, and discussions.
We provide and present clinical collaboration with specialists from various disciplines. Each specialist is governed by their professional scope of practice and their jurisdiction of licensure. We use functional health & wellness protocols to treat and support care for the injuries or disorders of the musculoskeletal system.
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Our office has reasonably attempted to provide supportive citations and has identified the relevant research study or studies supporting our posts. We provide copies of supporting research studies available to regulatory boards and the public upon request.
We understand that we cover matters that require an additional explanation of how it may assist in a particular care plan or treatment protocol; therefore, to further discuss the subject matter above, please feel free to ask Dr. Alex Jimenez, DC, or contact us at 915-850-0900.
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Dr. Alex Jimenez DC, MSACP, RN*, CCST, IFMCP*, CIFM*, ATN*
email: coach@elpasofunctionalmedicine.com
Licensed as a Doctor of Chiropractic (DC) in Texas & New Mexico*
Texas DC License # TX5807, New Mexico DC License # NM-DC2182
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Florida License RN License # RN9617241 (Control No. 3558029)
Compact Status: Multi-State License: Authorized to Practice in 40 States*
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Dr. Alex Jimenez DC, MSACP, RN* CIFM*, IFMCP*, ATN*, CCST
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