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. 2016 May;68(5):1290-1300.
doi: 10.1002/art.39560.

X Chromosome Dose and Sex Bias in Autoimmune Diseases: Increased Prevalence of 47,XXX in Systemic Lupus Erythematosus and Sjögren's Syndrome

Ke Liu  1   2 Biji T Kurien  3   4   5 Sarah L Zimmerman  6 Kenneth M Kaufman  1   7 Diana H Taft  1 Leah C Kottyan  1 Sara Lazaro  1 Carrie A Weaver  1 John A Ice  4 Adam J Adler  4   5 James Chodosh  8 Lida Radfar  9 Astrid Rasmussen  4 Donald U Stone  10 David M Lewis  9 Shibo Li  3 Kristi A Koelsch  3   4 Ann Igoe  3   4 Mitali Talsania  3 Jay Kumar  3   4 Jacen S Maier-Moore  3   4   5   11 Valerie M Harris  3   4 Rajaram Gopalakrishnan  12 Roland Jonsson  13   14 James A Lessard  15 Xianglan Lu  3 Jacques-Eric Gottenberg  16 Juan-Manuel Anaya  17 Deborah S Cunninghame-Graham  18 Andrew J W Huang  12 Michael T Brennan  19 Pamela Hughes  12 Gabor G Illei  20 Corinne Miceli-Richard  21 Edward C Keystone  22 Vivian P Bykerk  23 Gideon Hirschfield  24 Gang Xie  25 Wan-Fai Ng  26 Gunnel Nordmark  27 Per Eriksson  28 Roald Omdal  29 Nelson L Rhodus  30 Maureen Rischmueller  31   32 Michael Rohrer  12 Barbara M Segal  33 Timothy J Vyse  18 Marie Wahren-Herlenius  34 Torsten Witte  35 Bernardo Pons-Estel  36 Marta E Alarcon-Riquelme  4   37 Joel M Guthridge  3   4 Judith A James  3   4 Christopher J Lessard  3   4 Jennifer A Kelly  4 Susan D Thompson  1 Patrick M Gaffney  4 Courtney G Montgomery  4 Jeffrey C Edberg  38 Robert P Kimberly  38 Graciela S Alarcón  38 Carl L Langefeld  39 Gary S Gilkeson  40   41 Diane L Kamen  40 Betty P Tsao  42 W Joseph McCune  43 Jane E Salmon  44 Joan T Merrill  3 Michael H Weisman  45 Daniel J Wallace  45 Tammy O Utset  46 Erwin P Bottinger  47 Christopher I Amos  48 Katherine A Siminovitch  25 Xavier Mariette  49 Kathy L Sivils  3   4 John B Harley #  1   2   7 R Hal Scofield #  3   4   5
Affiliations

X Chromosome Dose and Sex Bias in Autoimmune Diseases: Increased Prevalence of 47,XXX in Systemic Lupus Erythematosus and Sjögren's Syndrome

Ke Liu et al. Arthritis Rheumatol. 2016 May.

Abstract

Objective: More than 80% of autoimmune disease predominantly affects females, but the mechanism for this female bias is poorly understood. We suspected that an X chromosome dose effect accounts for this, and we undertook this study to test our hypothesis that trisomy X (47,XXX; occurring in ∼1 in 1,000 live female births) would be increased in patients with female-predominant diseases (systemic lupus erythematosus [SLE], primary Sjögren's syndrome [SS], primary biliary cirrhosis, and rheumatoid arthritis [RA]) compared to patients with diseases without female predominance (sarcoidosis) and compared to controls.

Methods: All subjects in this study were female. We identified subjects with 47,XXX using aggregate data from single-nucleotide polymorphism arrays, and, when possible, we confirmed the presence of 47,XXX using fluorescence in situ hybridization or quantitative polymerase chain reaction.

Results: We found 47,XXX in 7 of 2,826 SLE patients and in 3 of 1,033 SS patients, but in only 2 of 7,074 controls (odds ratio in the SLE and primary SS groups 8.78 [95% confidence interval 1.67-86.79], P = 0.003 and odds ratio 10.29 [95% confidence interval 1.18-123.47], P = 0.02, respectively). One in 404 women with SLE and 1 in 344 women with SS had 47,XXX. There was an excess of 47,XXX among SLE and SS patients.

Conclusion: The estimated prevalence of SLE and SS in women with 47,XXX was ∼2.5 and ∼2.9 times higher, respectively, than that in women with 46,XX and ∼25 and ∼41 times higher, respectively, than that in men with 46,XY. No statistically significant increase of 47,XXX was observed in other female-biased diseases (primary biliary cirrhosis or RA), supporting the idea of multiple pathways to sex bias in autoimmunity.

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Figures

Fig. 1
Fig. 1. 47,XXX identification
B allele frequency and logR ratio plot of 46,XY from a representative normal man (first panel, for comparison purposes only as men were not included in the present study), 46,XX from a normal woman (second panel) and 47,XXX from a trisomy X syndrome patient (third panel).
Fig. 2
Fig. 2. 47,XXX validation by fluorescence in situ hybridization assay (FISH)
Validation of 46,XX from a normal female (upper) and 47,XXX from a trisomy X syndrome patient (bottom). The images are showing a single representative nucleus. 200 nuclei were counted.
Fig. 3
Fig. 3. 47,XXX validation by PCR
DNA amplification validation of 47,XXX for two systemic lupus erythematosus patients (SLE1, SLE2), two primary Sjögren's syndrome patients (SS1, SS2) and one primary biliary cirrhosis patient (PBC1). As calibrators, we used known 47,XXX (shown in blue), 46,XX (shown in red) and 45X (shown in purple) samples. Calibrators were all validated by FISH and used to determine copy number in the experimental samples.

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