Activate Now
 
ProHealth fibromyalgia Vitamin and Natural Supplement Store and Health
Home  |  Log In  |  My Account  |  View Cart  View Your ProHealth Vitamin and Supplement Shopping Cart
800-366-6056  |  Contact Us  |  Help
Facebook Google Plus
Fibromyalgia  Chronic Fatigue Syndrome & M.E.  Lyme Disease  Natural Wellness  Supplement News  Forums  Our Story
Store     Brands   |   A-Z Index   |   Best Sellers   |   New Products   |   Deals & Specials   |   Under $10   |   SmartSavings Club

Trending News

Optic Nerve Thinning Suggests Fibromyalgia is “Neurodegenerative” Disease

Fibromyalgia: The body holding on to past trauma

10 Fast Facts: Fibromyalgia Is Real

Top 10 Mood-Boosting Foods for Fibromyalgia

Ten Tips to Simplify, Lower the Cost, and Optimize CFS and fibromyalgia Treatment

Patient Insights into the Design of Technology to Support a Strengths-Based Approach to Health Care.

3 Genetic Reset Methods Your Doctor Should Prescribe for Fibromyalgia

How to Obtain Relief for Fibromyalgia - Part 1: Complementary and Alternative Therapies

Keep Learning – Even From Bed!

Fibromyalgia Is Correlated with Retinal Nerve Fiber Layer Thinning.

 
Print Page
Email Article

Fibromyalgia Symptoms Associated with Gene Variant

  [ 13 votes ]   [ 1 Comment ]
www.ProHealth.com • April 28, 2014


Editor's comment: Catechol-O-methyltransferase is one of several enzymes involved in the degradation or inactivation of the catecholamine neurotransmitters (dopamine, epinephrine, and norepinephrine). In humans, the catechol-O-methyltransferase protein is encoded by the COMT gene. The Val158Met polymorphism is a gene variant that breaks down dopamine much faster than normal and is thought to modulate dopamine signaling in the brain's frontal lobes. This gene variant has been shown to affect cognitive tasks and may be relevant for emotional processing. The results of this study found an association between this gene variant and certain fibromyalgia symptoms.

Clinical symptoms in fibromyalgia are associated to catechol-O-methyltransferase (COMT) gene Val158Met polymorphism.

By A. Inanir, et al.

Abstract:

1.?Fibromyalgia syndrome (FMS) is a common chronic widespread pain syndrome mainly affecting women. The aim of this study was to explore the frequency and clinical significance of catechol-O-methyltransferase (COMT) gene Val158Met polymorphism in a large cohort of Turkish patients with FMS.

2.?The study included 379 FMS patients and 290 controls. Genomic DNA was isolated and genotyped using polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP) analyses.

3.?The genotype frequencies of Val158Met polymorphism showed a small difference between FMS patients and healthy controls (p?=?0.047), however, the Met/Met genotype was significantly higher in FMS patients than healthy controls (p?=?0.016). No difference was observed for allele frequencies between two groups. Stratification analysis according to clinical features for this disease reveals that weight, FMS Impact Questionnaire score, algometry and Raynaud's syndrome, were detected to have statistically significant associations with Val158Met polymorphism (p?=?0.037, p?=?0.042, p?=?0.039 and p?=?0.033, respectively). Pain sensitivity, measured by algometry, was statistically higher in patients with Met/Met genotype than the patients with Val/Val and Val/Met genotypes (p?=?0.017).

4.?The results of this study suggested that COMT gene Val158Met polymorphism is positively associated with FMS and play a relevant role in the clinical symptoms of the disease.

Source: Xenobiotica, April 24, 2014. By A. Inanir, N. Karakus, O. Ates, S. Sezer, N. Bozkurt, S. Inanir and S. Yigit. Department of Physical Therapy and Rehabilitation, Faculty of Medicine.




Post a Comment

Featured Products From the ProHealth Store
Hydroxocobalamin Extreme™ FibroSleep™ Fibro Freedom™

Looking for Vitamins, Herbs and Supplements?
Search the ProHealth Store for Hundreds of Natural Health Products


Article Comments Post a Comment

Gene Variant
Posted by: elvis321
Apr 29, 2014
I do find this study interesting, and wonder if??? there is anything to indicate Frontal Lobe dysfunction may also be due to birth trauma ie: lack of oxygen, resuscitation post birth etc that causes a brain injury. Is is strictly the gene? There is trending of this in children with ADHD. I'm thinking there is a correlation.
I guess I'd also like to know...what's this now going to do for those of us already diagnosed? O.K. if you now know a cause...but what makes it different, can be done? Still nothing.
Reply Reply
 
Natural Pain Relief Supplements

Featured Products

B-12 Extreme™ B-12 Extreme™
The Most Potent Vitamin B-12 on Earth
Hydroxocobalamin Extreme™ Hydroxocobalamin Extreme™
The B-12 Your Brain Needs for Detox & Sharpness
Fibro Freedom™ Fibro Freedom™
Soothes, Strengthens & Revitalizes
FibroSleep™ FibroSleep™
The All-in-One Natural Sleep Aid
Guaifenesin FA™ Guaifenesin FA™
Helps the Body Eliminate Excess Calcium and Phosphates

Natural Remedies

Everything You Always Wanted to Know About Sleep But Were Too Tired to Ask Everything You Always Wanted to Know About Sleep But Were Too Tired to Ask
Dreaming of a Good Night's Sleep? Dreaming of a Good Night's Sleep?
Astaxanthin - A Little-Known but Power-Packed Nutrient Astaxanthin - A Little-Known but Power-Packed Nutrient
Guarding Against the Dangers of Vitamin D Deficiency Guarding Against the Dangers of Vitamin D Deficiency
Reversing Neurodegeneration with a New Magnesium Compound Reversing Neurodegeneration with a New Magnesium Compound

CONTACT US
ProHealth, Inc.
555 Maple Ave
Carpinteria, CA 93013
(800) 366-6056  |  Email

· Become a Wholesaler
· Vendor Inquiries
· Affiliate Program
SHOP WITH CONFIDENCE
Credit Card Processing
SUBSCRIBE AND SAVE 15% NOW*
Be the first to know about new products, special discounts and the latest health news. *New subscribers only

CONNECT WITH US ProHealth on Facebook  ProHealth on Twitter  ProHealth on Pinterest  ProHealth on Google Plus

© 2016 ProHealth, Inc. All rights reserved. Pain Tracker App  |  Store  |  Customer Service  |  Guarantee  |  Privacy  |  Contact Us  |  Library  |  RSS  |  Site Map