The Comorbid Association of Migraine with Osteoarthritis and Hypertension Complement C3F and Berkson's Bias

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 f...

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Published inCephalalgia Vol. 17; no. 1; pp. 23 - 26
Main Authors Peroutka, SJ, Price, SC, Jones, KW
Format Journal Article
LanguageEnglish
Published London, England SAGE Publications 01.02.1997
Blackwell Science Ltd
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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.
AbstractList 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.
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 &lt; 0.0008) and hypertension (Chi square = 5.18; p &lt; 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.
Author Jones, KW
Price, SC
Peroutka, SJ
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  publication-title: Neurology
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  contributor:
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  doi: 10.1038/2141042a0
– volume-title: The history and geography of human genes
  year: 1994
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  contributor:
    fullname: Cavalli-Sforza LL
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  doi: 10.1136/ard.49.4.225
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  doi: 10.1111/j.1526-4610.1989.hed2901049.x
– ident: bibr28-j.1468-2982.1997.1701023.x
  doi: 10.2307/3002000
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Snippet 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....
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SubjectTerms Comorbidity
Complement C3c - genetics
Coronary Disease - complications
Coronary Disease - epidemiology
Coronary Disease - genetics
Genotype
Humans
Hypertension - complications
Hypertension - epidemiology
Hypertension - genetics
Migraine Disorders - complications
Migraine Disorders - epidemiology
Migraine Disorders - genetics
Osteoarthritis - complications
Osteoarthritis - epidemiology
Osteoarthritis - genetics
Polymorphism, Genetic
Subtitle Complement C3F and Berkson's Bias
Title The Comorbid Association of Migraine with Osteoarthritis and Hypertension
URI https://journals.sagepub.com/doi/full/10.1046/j.1468-2982.1997.1701023.x
https://onlinelibrary.wiley.com/doi/abs/10.1046%2Fj.1468-2982.1997.1701023.x
https://www.ncbi.nlm.nih.gov/pubmed/9051331
https://search.proquest.com/docview/78854116
Volume 17
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