Join Here   |   Log In
Black Friday Sale (Early!)   Use the Coupon Code BlackFriday for 20% off any membership!

News and Research: Mitochondrial polymorphism linked to fibromyalgia

Title: A genetic polymorphism that is associated with mitochondrial energy metabolism increases risk of fibromyalgia  July 2002

Journal: Journal of the International Association for the Study of Pain

This new study looked at both the full nuclear genome and mitochondrial genome for 609 people. The patients in the study had persistent pain conditions (e.g. fibromyalgia, IBS, TMJ, or vulvar vestibulitis).

Fibromyalgia is a syndrome of widespread muscle pain. People with fibromyalgia often are fatigued and have sleep or mood issues also.

The researcher found that one SNP in a mitochondrial gene (m.2352) increased the risk of fibromyalgia almost 5-fold. The researchers then replicated the link with this mitochondrial genetic variant and other pain disorders.

The abstract explains the importance of this finding:

Essentially, oxidative phosphorylation is what is going on in the mitochondria to produce most of the ATP that a cell needs. With a decreased membrane potential, the mitochondria will not be as efficient.

Why is this important? The study directly links fibromyalgia to cellular metabolism. Therapies that target boosting the mitochondria may be effective.

This one genetic variant in the mitochondrial DNA is likely not the whole picture for fibromyalgia and other pain disorders, but it does point to a pathway or mechanism of action.

 

 

 


About the Author:
Debbie Moon is the founder of Genetic Lifehacks. Fascinated by the connections between genes, diet, and health, her goal is to help you understand how to apply genetics to your diet and lifestyle decisions. Debbie has a BS in engineering from Colorado School of Mines and an MSc in biological sciences from Clemson University. Debbie combines an engineering mindset with a biological systems approach to help you understand how genetic differences impact your optimal health.