Xie Shangdan, Jiang Mengying, Liu Hejing, Xue Fang, Chen Xin, Zhu Xueqiong
Department of Obstetrics and Gynecology, The Second Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Front Genet. 2022 Jun 20;13:844684. doi: 10.3389/fgene.2022.844684. eCollection 2022.
Uterine leiomyomas (ULs) is the most common gynecological benign tumor in women. Our previous study showed that the phenomenon of vitamin D deficiency existed in patients with ULs. However, the association of vitamin D anabolism-related gene polymorphisms and susceptibility to ULs was unclear. Vitamin D anabolism-related gene polymorphisms in 110 patients with ULs and 110 healthy controls were detected by sequencing and the differences of the 92 SNPs were analyzed in the two groups chi-square test. To verify the association between the significantly different SNPs and the risk of ULs, the SNPs were genotyped in another 340 patients and 340 healthy controls. Additionally, an unconditional logistic regression model was conducted to calculate the odds ratio (OR) of ULs occurrence and the 95% confidence interval (CI), adjusting for age and BMI. In sequencing samples, there were differences in DHCR7 rs1044482 C > T ( = 0.008) and NADSYN1 rs2276360 G > C ( = 0.025) between patients with ULs and healthy controls. DHCR7 rs1044482 was related to the susceptibility to ULs in validation samples (heterogeneous: adjusted OR = 1.967, = 0.002; homogenous: adjusted OR = 2.494, = 0.002; additive: adjusted OR = 1.485, < 0.041; and dominant: adjusted OR = 2.084, < 0.001). Stratified analysis further showed that the DHCR7 rs1044482 polymorphisms were associated with ULs risks in women over 40 and with 18.5-25.0 BMI. In contrast to the wild-type CG haplotype vectors, individuals with TC haplotypes had a higher risk of developing ULs. The vitamin D anabolism-related gene DHCR7 rs1044482 C > T polymorphism was a risk factor of ULs, especially in patients over 40 with 18.5-25.0 BMI, while the relationship between NADSYN1 rs2276360 and ULs risk was not clear.
子宫肌瘤(ULs)是女性最常见的妇科良性肿瘤。我们之前的研究表明,子宫肌瘤患者存在维生素D缺乏现象。然而,维生素D合成代谢相关基因多态性与子宫肌瘤易感性之间的关联尚不清楚。通过测序检测了110例子宫肌瘤患者和110例健康对照者的维生素D合成代谢相关基因多态性,并采用卡方检验分析了两组中92个单核苷酸多态性(SNPs)的差异。为了验证显著不同的SNPs与子宫肌瘤风险之间的关联,在另外340例患者和340例健康对照者中对这些SNPs进行基因分型。此外,进行无条件逻辑回归模型以计算子宫肌瘤发生的比值比(OR)和95%置信区间(CI),并对年龄和体重指数(BMI)进行校正。在测序样本中,子宫肌瘤患者与健康对照者之间在DHCR7 rs1044482 C>T(P = 0.008)和NADSYN1 rs2276360 G>C(P = 0.025)存在差异。DHCR7 rs1044482与验证样本中子宫肌瘤的易感性相关(异质性:校正OR = 1.967,P = 0.002;同质性:校正OR = 2.494,P = 0.002;加性:校正OR = 1.485,P < 0.041;显性:校正OR = 2.084,P < 0.001)。分层分析进一步表明,DHCR7 rs1044482多态性与40岁以上且BMI为18.5 - 25.0的女性子宫肌瘤风险相关。与野生型CG单倍型载体相比,携带TC单倍型的个体患子宫肌瘤的风险更高。维生素D合成代谢相关基因DHCR7 rs1044482 C>T多态性是子宫肌瘤发生的危险因素,尤其是在40岁以上且BMI为18.5 - 25.0的患者中,而NADSYN1 rs2276360与子宫肌瘤风险之间的关系尚不清楚。