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唐氏综合征儿童桥本甲状腺炎中细胞毒性 T 淋巴细胞相关蛋白 4 +49A/G 多态性。

Cytotoxic T-lymphocyte-associated protein 4 +49A/G polymorphism in Down syndrome children with Hashimoto's thyroiditis.

机构信息

Faculty of Medicine, Department of Child Health, Dr. Soetomo General Hospital, Universitas Airlangga, Surabaya, East Java, Indonesia.

Faculty of Medicine, Universitas Airlangga, Surabaya, East Java, Indonesia.

出版信息

Biomol Biomed. 2023 Jul 3;23(4):634-639. doi: 10.17305/bb.2022.7869.

Abstract

Thyroid dysfunction is the most common endocrine disorder in Down syndrome (DS) children. Cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4) is one of the immune regulatory genes that correlates with Hashimoto's thyroiditis (HT). However, studies on CTLA-4 +49A/G in DS children with HT are still limited. We aimed to evaluate CTLA-4 +49A/G gene polymorphism in DS children with HT. This case-control study, conducted from February 2020 to February 2022 at Dr. Soetomo General Hospital, Surabaya, enrolled 40 DS children with HT and 50 healthy children. The DNA sequencing was performed to identify the polymorphism (Sanger sequencing). Thyroid peroxidase antibodies (TPOAb), thyroglobulin antibodies (TgAb), thyroid-stimulating hormone (TSH), and free thyroxine (FT4) levels were analyzed by enzyme-linked immunosorbent assay (ELISA). The mean age of DS children with HT was 1.78 years. Males predominated in the study population. Subjects with GG genotype were diagnosed earliest with hypothyroidism (8 months) compared with other studies. The most common thyroid dysfunction was central hypothyroidism, with TgAb positivity present in all patients. The AA genotype (odds ratio [OR] 0.265, 95% confidence interval [CI] 0.094-0.746; P = 0.012) and A allele (OR 0.472, 95% CI 0.309-0.721; P = 0.0002) were significantly more frequent in the control group. The AG genotype (OR 2.65, 95% CI 0.094-0.746; P = 0.003) and G allele (OR 2.116, 95% CI 1.386-3.23; P = 0.003) were more frequent in the DS with HT group. The age of the subjects in this study was younger than in previous studies. The AG genotype and the G allele were more prevalent in the DS with HT group and may be a risk factor in HT development in DS children. Furthermore, the AA genotype may act as a protective factor against HT in DS children.

摘要

甲状腺功能障碍是唐氏综合征(DS)儿童中最常见的内分泌疾病。细胞毒性 T 淋巴细胞相关抗原 4(CTLA-4)是与桥本甲状腺炎(HT)相关的免疫调节基因之一。然而,关于 DS 儿童 HT 中 CTLA-4+49A/G 的研究仍然有限。我们旨在评估 HT 中 DS 儿童的 CTLA-4+49A/G 基因多态性。这项病例对照研究于 2020 年 2 月至 2022 年 2 月在泗水苏托莫综合医院进行,共纳入 40 名 HT 合并 DS 的儿童和 50 名健康儿童。通过 DNA 测序(Sanger 测序)鉴定多态性。酶联免疫吸附试验(ELISA)分析甲状腺过氧化物酶抗体(TPOAb)、甲状腺球蛋白抗体(TgAb)、促甲状腺激素(TSH)和游离甲状腺素(FT4)水平。HT 合并 DS 儿童的平均年龄为 1.78 岁。研究人群中男性居多。与其他研究相比,GG 基因型的受试者最早被诊断为甲状腺功能减退(8 个月)。最常见的甲状腺功能障碍是中枢性甲状腺功能减退,所有患者的 TgAb 均为阳性。AA 基因型(比值比 [OR] 0.265,95%置信区间 [CI] 0.094-0.746;P=0.012)和 A 等位基因(OR 0.472,95%CI 0.309-0.721;P=0.0002)在对照组中更为常见。AG 基因型(OR 2.65,95%CI 0.094-0.746;P=0.003)和 G 等位基因(OR 2.116,95%CI 1.386-3.23;P=0.003)在 HT 合并 DS 组中更为常见。本研究中受试者的年龄小于以往研究。AG 基因型和 G 等位基因在 HT 合并 DS 组中更为常见,可能是 DS 儿童 HT 发病的危险因素。此外,AA 基因型可能是 DS 儿童 HT 的保护因素。

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