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基因多态性对多发性硬化易感性及多学科康复反应的性别特异性影响。

Sex-Specific Effects of Gene Polymorphisms on Multiple Sclerosis Susceptibility and Response to Multidisciplinary Rehabilitation.

作者信息

Agliardi Cristina, Guerini Franca Rosa, Zanzottera Milena, Bolognesi Elisabetta, Caputo Domenico, Groppo Elisabetta, Rovaris Marco, Clerici Mario

机构信息

IRCCS Fondazione Don Carlo Gnocchi ONLUS, Via Capecelatro 66, 20148 Milan, Italy.

Clinical Neurology Unit, Department of Health Sciences, Ospedale San Paolo, ASST Santi Paolo e Carlo, University of Milan, 20142 Milan, Italy.

出版信息

Int J Mol Sci. 2025 Sep 12;26(18):8915. doi: 10.3390/ijms26188915.

Abstract

Multiple sclerosis (MS) is an inflammatory demyelinating disease of the central nervous system that affects young adults with different clinical phenotypes: relapsing-remitting MS (RR-MS), secondary progressive MS (SP-MS), and primary progressive MS (PP-MS). Aquaporin 4 (AQP4), a protein found in astrocytes, plays a crucial role in CNS functions. We investigated the possible association of three gene single-nucleotide polymorphisms (SNPs), rs2075575, rs162009, and rs335929, with MS risk and rehabilitation outcomes. SNPs were genotyped in 237 people with MS (pwMS), spanning all disease forms and enrolled in an intensive, multidisciplinary rehabilitation program, and 461 healthy controls (HCs). The rs2075575 GG genotype was significantly less frequent in male pwRR-MS compared to HCs (15.4% vs. 29.1%, = 0.033, OR = 0.44), suggesting a protective role. Haplotype analysis identified the rs2075575(A)-rs162009(A)-rs335929(C) (A-A-C) haplotype as an MS risk factor, particularly in males ( = 0.001, OR = 2.70). Finally, the rs335929 SNP was significantly associated with EDSS improvement after rehabilitation ( = 0.011), with the CC genotype showing the highest mean ΔEDSS in pwRR-MS ( = 0.009), especially in males ( = 0.003). gene SNPs may influence both MS susceptibility and rehabilitation outcomes, with sex-specific effects. Further studies are needed to understand the mechanisms behind these associations and their potential for personalized treatment strategies in MS.

摘要

多发性硬化症(MS)是一种中枢神经系统的炎性脱髓鞘疾病,影响具有不同临床表型的年轻人:复发缓解型多发性硬化症(RR-MS)、继发进展型多发性硬化症(SP-MS)和原发进展型多发性硬化症(PP-MS)。水通道蛋白4(AQP4)是一种在星形胶质细胞中发现的蛋白质,在中枢神经系统功能中起关键作用。我们研究了三个基因单核苷酸多态性(SNP),即rs2075575、rs162009和rs335929与MS风险及康复结局之间的可能关联。对237例患有MS的患者(pwMS)进行了SNP基因分型,这些患者涵盖了所有疾病形式,并参加了一个强化的多学科康复项目,同时对461名健康对照者(HCs)进行了基因分型。与HCs相比,男性pwRR-MS中rs2075575 GG基因型的频率显著更低(15.4%对29.1%,P = 0.033,OR = 0.44),表明具有保护作用。单倍型分析确定rs2075575(A)-rs162009(A)-rs335929(C)(A-A-C)单倍型为MS风险因素,尤其是在男性中(P = 0.001,OR = 2.70)。最后,rs335929 SNP与康复后扩展残疾状态量表(EDSS)的改善显著相关(P = 0.011),CC基因型在pwRR-MS中显示出最高的平均EDSS变化值(P = 0.009),尤其是在男性中(P = 0.003)。基因SNP可能影响MS易感性和康复结局,且存在性别特异性效应。需要进一步研究以了解这些关联背后的机制及其在MS个性化治疗策略中的潜力。

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