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昼夜节律基因ARNTL/BMAL1和CLOCK与多发性硬化症的关联。

Association of circadian rhythm genes ARNTL/BMAL1 and CLOCK with multiple sclerosis.

作者信息

Lavtar Polona, Rudolf Gorazd, Maver Aleš, Hodžić Alenka, Starčević Čizmarević Nada, Živković Maja, Šega Jazbec Saša, Klemenc Ketiš Zalika, Kapović Miljenko, Dinčić Evica, Raičević Ranko, Sepčić Juraj, Lovrečić Luca, Stanković Aleksandra, Ristić Smiljana, Peterlin Borut

机构信息

Clinical Institute of Medical Genetics, University Medical Centre Ljubljana, Ljubljana, Slovenia.

Departments of Biology and Medical Genetics, School of Medicine, University of Rijeka, Rijeka, Croatia.

出版信息

PLoS One. 2018 Jan 11;13(1):e0190601. doi: 10.1371/journal.pone.0190601. eCollection 2018.

Abstract

Prevalence of multiple sclerosis varies with geographic latitude. We hypothesized that this fact might be partially associated with the influence of latitude on circadian rhythm and consequently that genetic variability of key circadian rhythm regulators, ARNTL and CLOCK genes, might contribute to the risk for multiple sclerosis. Our aim was to analyse selected polymorphisms of ARNTL and CLOCK, and their association with multiple sclerosis. A total of 900 Caucasian patients and 1024 healthy controls were compared for genetic signature at 8 SNPs, 4 for each of both genes. We found a statistically significant difference in genotype (ARNTL rs3789327, P = 7.5·10-5; CLOCK rs6811520 P = 0.02) distributions in patients and controls. The ARNTL rs3789327 CC genotype was associated with higher risk for multiple sclerosis at an OR of 1.67 (95% CI 1.35-2.07, P = 0.0001) and the CLOCK rs6811520 genotype CC at an OR of 1.40 (95% CI 1.13-1.73, P = 0.002). The results of this study suggest that genetic variability in the ARNTL and CLOCK genes might be associated with risk for multiple sclerosis.

摘要

多发性硬化症的患病率随地理纬度而变化。我们推测这一事实可能部分与纬度对昼夜节律的影响有关,因此昼夜节律关键调节因子ARNTL和CLOCK基因的遗传变异可能会增加患多发性硬化症的风险。我们的目的是分析ARNTL和CLOCK基因的特定多态性及其与多发性硬化症的关联。我们比较了900名白种人患者和1024名健康对照者在8个单核苷酸多态性(SNP)位点的基因特征,每个基因各4个SNP。我们发现患者和对照者的基因型分布(ARNTL基因的rs3789327,P = 7.5·10-5;CLOCK基因的rs6811520,P = 0.02)存在统计学显著差异。ARNTL基因的rs3789327位点CC基因型与多发性硬化症的较高风险相关,比值比(OR)为1.67(95%置信区间1.35 - 2.07,P = 0.0001),CLOCK基因的rs6811520位点CC基因型的OR为1.40(95%置信区间1.13 - 1.73,P = 0.002)。本研究结果表明,ARNTL和CLOCK基因的遗传变异可能与多发性硬化症的风险相关。

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本文引用的文献

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Mult Scler. 2015 Aug;21(9):1195-9. doi: 10.1177/1352458514563592. Epub 2015 Feb 19.
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