Is Fibromyalgia Hereditary?

Understanding Clustering in Families

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Is Fibromyalgia Hereditary?

"Several people in my family have had fibromyalgia and now I'm showing a lot of the symptoms. That makes me really worried about my kids -- have I doomed them to this? Is fibromyalgia hereditary?"


This is a common concern. It's scary to think that we may have, unwittingly, passed a chronic, debilitating illness along to our children. While they may have an elevated risk, though, they are absolutely not guaranteed to develop fibromyalgia.

Here's a look at why:

Based on research, the current belief is that fibromyalgia is not hereditary in the classical sense, where a mutation of a single gene is responsible for a given trait. That's called monogenic, and it controls things like blue eye color; however, evidence does suggest that your genes can predispose you to fibromyalgia, but in a complex way involving many genes, which is called polygenic.

What's the Difference?

In a classical monogenic hereditary condition, the specific genes you get from your parents are the primary determining factor in whether you'll get a disease. For example, in cystic fibrosis, the child of parents who are both disease carriers has a 25% chance of developing cystic fibrosis. They either get the right genetic mutation or they don't.

With polygenic predisposition, it's not as simple or as certain because your genes only mean that a particular illness is possible under the right conditions.

Typically, other factors come into play to actually trigger an illness.

In fibromyalgia, these other factors may include other sources of chronic pain, autoimmune disease, sleep disorders, chronic stress, infectious illness, or abnormal brain chemistry. Some experts hypothesize that environmental things such as food sensitivities or exposure to toxins could also play a role.

That means your child may have inherited a genetic predisposition for fibromyalgia, but that still doesn't mean he or she will end up with it. It would take an additional set of circumstances to take them down that path.

Genetic Links in Fibromyalgia

Researchers began looking into a possible genetic component of fibromyalgia long ago because it does tend to run in families, in what are called "clusters." A 1989 study looked at siblings and parents of fibromyalgia patients and found that 52% of them had characteristic symptoms and other findings of fibromyalgia but had not been diagnosed with it. Another 22% didn't have symptoms but did have evidence of abnormal muscle consistency.

Later research confirmed the high rate of occurrence in families and showed that low pain threshold (the point at which sensation becomes painful) also appeared common in relatives of people with fibromyalgia.

We're really just beginning to get a picture of the specific genetic factors associated with fibromyalgia.

So far, we have multiple studies suggesting connections with numerous genes but many of these studies have not been replicated.

Genetic abnormalities that have been suggested by preliminary studies include genes that deal with neurotransmitters (chemical messengers in the brain) that have been implicated in fibromyalgia, including serotonin, norepinephrine, dopamine, GABA and glutamate. Others are involved in general brain function, fighting viral infection, and brain receptors that deal with opioids (narcotic pain killers) and cannabinoids (such as marijuana.)

As we learn more about these genetic associations, researchers may identify which of them contributes to the risk of developing fibromyalgia as well as whether any can be used to diagnose or treat the condition.


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