The comorbid association of migraine with osteoarthritis and hypertension: complement C3F and Berkson's bias.

Abstract

Migraine is known to have a major genetic component and has been associated with a wide variety of comorbid disorders including arthritis and heart disease. Since migraine and some of its comorbid disorders involve inflammation, complement C3, a protein involved in acute inflammation, was selected for analysis as a candidate gene in an ongoing study of the genetic basis of migraine. Polymorphism frequencies for complement C3F (0.19) and C3S (0.81) in a sample of 137 unrelated migraineurs were found to be consistent with a control group as well as previous population studies, indicating that this common polymorphism has no association with migraine susceptibility. However, C3F positive individuals with migraine were found to have an increased incidence of osteoarthritis (Chi square = 10.06; p < 0.0008) and hypertension (Chi square = 5.18; p < 0.01). Therefore, the data in the present study indicate that certain migraine comorbidities that have been reported in the literature may result from Berkson's bias as opposed to a shared pathophysiological variation in the C3 gene.

• Authors: S J Peroutka, S C Price, K W Jones
• Journal: Cephalalgia : an international journal of headache (Cephalalgia) Vol. 17 Issue 1 Pg. 23-6 (Feb 1997) ISSN: 0333-1024 [Print] England
• PMID: 9051331 (Publication Type: Journal Article)

Chemical References

• Complement C3c

Topics

• Comorbidity
• Complement C3c (genetics)
• Coronary Disease (complications, epidemiology, genetics)
• Genotype
• Humans
• Hypertension (complications, epidemiology, genetics)
• Migraine Disorders (complications, epidemiology, genetics)
• Osteoarthritis (complications, epidemiology, genetics)
• Polymorphism, Genetic