Department of Neurology, Tianjin Huanhu Hospital, Tianjin Key Laboratory of Cerebrovascular and Neurodegenerative Diseases, Tianjin, China.
Department of Neurology, Tianjin Union Medical Center, Tianjin, China.
Brain Behav. 2023 May;13(5):e2960. doi: 10.1002/brb3.2960. Epub 2023 Mar 28.
Despite its public health importance, the causes of small vessel disease (SVD) are not fully understood. The presence of SVD in monogenic twins indicates the involvement of genetic factors in the pathogenesis of this disease. The purpose of this study was to investigate the association of methylenetetrahydrofolate reductase (MTHFR) gene polymorphisms with SVD risk.
Patients with SVD and matched controls were recruited from Tianjin Union Medical Center and Tianjin Huanhu Hospital. Clinical and laboratory data were collected. Plasma total homocysteine (tHcy) and folate levels were measured, and MTHFR rs1801133 (C677T) and rs1801131 (A1298C) single-nucleotide polymorphisms were genotyped. We analyzed potential associations among SVD and MTHFR polymorphisms, tHcy, and folate levels.
Patients with SVD displayed significantly decreased plasma folate levels (Z = -3.537, p < .001) and increased tHcy levels (Z = 4.910, p < .001) compared with controls. Significantly different plasma tHcy levels were associated with rs1801133 (χ = 6.664, p = .036), and post hoc analysis indicated higher plasma tHcy levels in individuals carrying the TT allele compared with levels in those carrying the TC allele (Z = 2.478, p = .013). No significant differences in tHcy levels were observed for rs1801131 alleles. The genotype and allele frequencies of rs1801133 were different between SVD and control groups (χ = 9.378, p = .009). There was no significant difference in distributions of rs1801131 genotypes between the two groups, and multivariable logistic regression analysis showed that rs1801131 and rs1801133 were not significantly associated with the risk of SVD.
Our study indicates that an elevated plasma tHcy level is independently associated with the development of SVD. Although MTHFR rs1801133 is linked to increased plasma homocysteine (Hcy) levels, it is not a risk factor for SVD. rs1801131 is not related to Hcy levels or SVD risk.
尽管小血管疾病(SVD)具有重要的公共卫生意义,但其病因尚不完全清楚。单基因双胞胎中 SVD 的存在表明遗传因素在该疾病的发病机制中起作用。本研究旨在探讨亚甲基四氢叶酸还原酶(MTHFR)基因多态性与 SVD 风险的关系。
我们从天津医科大学总医院和天津环湖医院招募了 SVD 患者和匹配的对照组。收集临床和实验室数据。测量血浆总同型半胱氨酸(tHcy)和叶酸水平,并对 MTHFR rs1801133(C677T)和 rs1801131(A1298C)单核苷酸多态性进行基因分型。我们分析了 SVD 与 MTHFR 多态性、tHcy 和叶酸水平之间的潜在关联。
与对照组相比,SVD 患者的血浆叶酸水平明显降低(Z = -3.537,p <.001),tHcy 水平明显升高(Z = 4.910,p <.001)。rs1801133 与血浆 tHcy 水平显著相关(χ ² = 6.664,p =.036),事后分析表明,携带 TT 等位基因的个体的血浆 tHcy 水平高于携带 TC 等位基因的个体(Z = 2.478,p =.013)。rs1801131 等位基因的 tHcy 水平无显著差异。rs1801133 的基因型和等位基因频率在 SVD 和对照组之间存在差异(χ ² = 9.378,p =.009)。两组 rs1801131 基因型的分布无显著差异,多变量逻辑回归分析显示 rs1801131 和 rs1801133 与 SVD 风险无显著相关性。
我们的研究表明,血浆 tHcy 水平升高与 SVD 的发生独立相关。虽然 MTHFR rs1801133 与血浆同型半胱氨酸(Hcy)水平升高有关,但它不是 SVD 的危险因素。rs1801131 与 Hcy 水平或 SVD 风险无关。