Evaluation relationship between VDR gene and clinical and inflammatory factors in patients with RRMS.

IF 1.8 Q3 MEDICINE, RESEARCH & EXPERIMENTAL European Journal of Translational Myology Pub Date : 2024-10-09 DOI:10.4081/ejtm.2024.12939
Maryam Milanifard, Soraya Mehrabi, Reza Ahadi, Mohsen Nabiuni, Samaneh Azimi Souteh, Mohammad Taghi Joghataei
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Abstract

Introduction: Adipocyte levels including leptin and FABS-4 levels, adiponectin, obesity, and vitamin D can be related to the occurrence and exacerbation of MS disease.

Objective: This research aimed at determining the relationship between VDR gene changes and clinical and inflammatory factors in patients with relapsing-remitting multiple sclerosis (RRMS).

Method: This case/control study was conducted based on the ethical principles of Helsinki. RRMS disease was confirmed based on history, clinical signs, radiological signs, and neurologist's diagnosis. The research population consisted of healthy people and patients with RRMS referring to Hazrat Rasool Akram Hospital between 2021 and 2023 who met the criteria for entering the research.

Results: FokI polymorphism is associated with a substantial increase in risk, with an odds ratio of 7.28, for those with the FF genotype who have RRMS compared to healthy individuals (OR=7.28: 95% CI; 1.86, 28.41). The presence of FokI polymorphism significantly raises the likelihood of developing RRMS in persons with the FF genotype compared to healthy individuals, with an odds ratio of 28.7. RRMS patients with genotypes did not exhibit a significant increase in risk compared to controls for FokI, ApaI, TaqI, and BsmI polymorphisms.

Conclusion: None of the studied polymorphisms revealed a significant risk in obese patients with different genotypes compared to the obese people. Further research, including more cases, is needed to avoid results that could be inflated by small samples or low frequencies of minor alleles.

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评估 RRMS 患者 VDR 基因与临床和炎症因素之间的关系。
导言:脂肪细胞水平(包括瘦素和FABS-4水平)、脂肪连通素、肥胖和维生素D可能与多发性硬化症的发生和加重有关:本研究旨在确定复发缓解型多发性硬化症(RRMS)患者 VDR 基因变化与临床和炎症因素之间的关系:这项病例/对照研究是根据赫尔辛基伦理原则进行的。根据病史、临床体征、放射学体征和神经科医生的诊断确认 RRMS 疾病。研究对象包括2021年至2023年期间在Hazrat Rasool Akram医院就诊的符合研究标准的健康人和RRMS患者:与健康人相比,FokI 多态性与 RRMS 风险大幅增加有关,FF 基因型 RRMS 患者的几率比为 7.28(OR=7.28:95% CI;1.86,28.41)。与健康人相比,FF基因型患者出现FokI多态性会显著增加患RRMS的可能性,几率比为28.7。与对照组相比,具有FokI、ApaI、TaqI和BsmI多态性基因型的RRMS患者的风险没有明显增加:结论:与肥胖人群相比,所研究的多态性在不同基因型的肥胖患者中均未显示出明显的风险。为了避免因样本少或小等位基因频率低而导致结果夸大,还需要进一步的研究,包括更多的病例。
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来源期刊
European Journal of Translational Myology
European Journal of Translational Myology MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
3.30
自引率
27.30%
发文量
74
审稿时长
10 weeks
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