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Skewed X chromosome inactivation in rheumatoid arthritis women
  1. Doua F Azzouz1,
  2. Onur Emre Onat2,
  3. Nathalie Balandraud1,3,
  4. Sami B Kanaan1,
  5. Jean Roudier1,3,
  6. Tayfun Ozcelik2,
  7. Nathalie C Lambert1
  1. 1INSERM UMR639, Marseille, France
  2. 2Department of Molecular Biology and Genetics, Bilkent University, Ankara, Turkey
  3. 3Rheumatology department, Hôpital La Conception, Marseille, France

Abstract

Background and objectives It has long been recognised that women have a greater prevalence of autoimmune diseases. Rheumatoid arthritis (RA) does not escape this rule with a women:men ratio of 3:1.

X chromosome inactivation (XCI) is a dosage compensation mechanism used by mammals to ensure that XX females and XY males equalise X chromosome gene expression. As a consequence, females are a mosaic of two cell lines, one expressing maternal X-linked and the other expressing paternal X-linked genes with a ratio close to 50:50 when XCI is random.

However skewing, defined as a deviation from the 50:50 ratio has been described in females with autoimmune thyroid diseases, scleroderma and juvenile idiopathic arthritis (for review1). The aim of the current study is to test whether women with RA also have a skewed XCI.

Methods The highly polymorphic CAG repeat on the first exon of the androgen receptor gene was genotyped, as described elsewhere2 to determine XCI bias in 84 women with RA and 100 healthy women.

Results A total of 54 patients and 69 controls were informative for androgen receptor polymorphism. Among them 31.5% of women with RA (17/54) had a skewed XCI (≥80:20) compared to only 17.4% of healthy women (12/69). Only extreme skewing was statistically significant with 18.5% of patients following this pattern and 2.9% of controls (p=0.004).

Conclusions Our preliminary data indicate that skewed XCI may be a risk factor for the occurrence of RA in women. Further studies need to be done to analyse whether women who have a skewed pattern have less genetic susceptibilities (shared epitope) or less specific autoantibodies (anti-CCP) as their risk factor is X chromosome linked.

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