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Whole-Exome Sequencing for Identification of Genetic Variants Involved in Vitamin D Metabolic Pathways in Families With Vitamin D Deficiency in Saudi Arabia.沙特阿拉伯维生素D缺乏家庭中用于鉴定参与维生素D代谢途径的基因变异的全外显子组测序
Front Genet. 2021 Jun 8;12:677780. doi: 10.3389/fgene.2021.677780. eCollection 2021.
4
Evaluation of vitamin D receptor expression in uterine leiomyoma and nonneoplastic myometrial tissue: a cross-sectional controlled study.评价子宫肌瘤和非肿瘤性子宫肌层组织中维生素 D 受体的表达:一项横断面对照研究。
Reprod Biol Endocrinol. 2021 May 5;19(1):67. doi: 10.1186/s12958-021-00752-x.
5
Vitamin D deficiency and uterine fibroids: an opportunity for treatment or prevention?维生素D缺乏与子宫肌瘤:治疗还是预防的契机?
Fertil Steril. 2021 May;115(5):1175-1176. doi: 10.1016/j.fertnstert.2021.02.040. Epub 2021 Mar 18.
6
An intronic DHCR7 genetic polymorphism associates with vitamin D serum level and incidence of acute coronary syndrome.内含子 DHCR7 基因多态性与维生素 D 血清水平和急性冠状动脉综合征的发生有关。
Steroids. 2021 May;169:108825. doi: 10.1016/j.steroids.2021.108825. Epub 2021 Mar 17.
7
rs12785878 T>C Polymorphism Is Associated With an Increased Risk of Early Onset of Alzheimer's Disease in Chinese Population.rs12785878基因T>C多态性与中国人群早发性阿尔茨海默病风险增加有关。
Front Genet. 2021 Feb 22;12:583695. doi: 10.3389/fgene.2021.583695. eCollection 2021.
8
The Effect of Vitamin D Deficiency on Overgrowth of Uterine Fibroids: A Blinded Randomized Clinical Trial.维生素D缺乏对子宫肌瘤过度生长的影响:一项双盲随机临床试验
Int J Fertil Steril. 2021 Apr;15(2):95-100. doi: 10.22074/IJFS.2020.134567. Epub 2021 Mar 11.
9
Vitamin D: Mechanism of Action and Biological Effects in Uterine Fibroids.维生素 D:在子宫肌瘤中的作用机制和生物学效应。
Nutrients. 2021 Feb 11;13(2):597. doi: 10.3390/nu13020597.
10
Candidate Genes for Age at Menarche Are Associated With Uterine Leiomyoma.初潮年龄的候选基因与子宫平滑肌瘤相关。
Front Genet. 2021 Jan 22;11:512940. doi: 10.3389/fgene.2020.512940. eCollection 2020.

维生素D合成相关基因多态性与子宫肌瘤易感性的关联

Association of Vitamin D Anabolism-Related Gene Polymorphisms and Susceptibility to Uterine Leiomyomas.

作者信息

Xie Shangdan, Jiang Mengying, Liu Hejing, Xue Fang, Chen Xin, Zhu Xueqiong

机构信息

Department of Obstetrics and Gynecology, The Second Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.

出版信息

Front Genet. 2022 Jun 20;13:844684. doi: 10.3389/fgene.2022.844684. eCollection 2022.

DOI:10.3389/fgene.2022.844684
PMID:35795205
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9251306/
Abstract

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.

摘要

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。