Suppr超能文献

1型糖尿病青少年的高血压、血压昼夜节律状态与[具体基因名称]基因多态性之间的关联

Association Between Hypertension, Dipping Status, and and Gene Polymorphisms in Adolescents with Type 1 Diabetes.

作者信息

Kovacevic Smiljka, Jesic Maja, Zdravkovic Vera, Djordjevic Stefan, Miolski Jelena, Gasic Vladimir, Jelovac Marina, Ugrin Milena, Pavlovic Sonja, Subosic Branko

机构信息

Endocrinology Department, University Children's Hospital, 11000 Belgrade, Serbia.

Faculty of Medicine, University of Belgrade, 11000 Belgrade, Serbia.

出版信息

Biomedicines. 2025 Mar 3;13(3):615. doi: 10.3390/biomedicines13030615.

Abstract

: This study aims to show the distribution of angiotensin-converting enzyme () rs1799752 (I>D) gene insertion/deletion () polymorphism and angiotensin II receptor type 1 () rs5186 (A>C) gene polymorphism in adolescents with hypertension (HT) and type 1 diabetes (T1D), as well as its association with hypertension and the diurnal variation of mean blood pressure (dipping phenomenon). : A cross-sectional study was conducted involving 118 adolescents diagnosed with T1D who underwent clinical and laboratory investigations, genetic analyses, and 24 h ambulatory blood pressure monitoring. The genotype frequencies were compared between adolescents with HT and those with normal blood pressure. Additionally, the genotype frequencies were compared between dippers and non-dippers. : Patients with HT were more likely to be female and exhibited significantly poorer glycemic control and higher triglycerides, along with increased body mass index and daily insulin dosage. The prevalence of genotypes in the hypertensive group was 20% II, 66.7% ID, and 13.3% DD, which did not significantly differ from the normal blood pressure group with 29.1% II, 53.4% ID, and 17.5% DD ( 0.625). The prevalence of genotypes in the hypertensive group was 53.3% AC, 40% AA, and 6.7% CC, which also did not significantly differ from the normal blood pressure group with 39.8% AC, 52.4% AA, and 7.8% CC ( 0.608). A total of 46% of the patients exhibited non-dipping phenomena. The prevalence of non-dippers among the genotypes was 13% DD, 33.3% II, and 53.7% ID ( 0.369), while for the genotypes, it was 50% AA, 42.6% AC, and 7.4% CC ( 0.976). : Our results indicate that in our adolescents with T1D, clinical and metabolic factors such as higher body mass index, triglycerides, suboptimal glycemic control, and female gender are more indicative of the development of hypertension than and gene polymorphisms. A potential reason for this finding could be the young age of the patients or the relatively small size of the study group. Future research involving larger sample sizes is needed to further investigate the genetic predisposition for the development of hypertension.

摘要

本研究旨在揭示高血压(HT)和1型糖尿病(T1D)青少年中血管紧张素转换酶()rs1799752(I>D)基因插入/缺失()多态性及血管紧张素II 1型受体()rs5186(A>C)基因多态性的分布情况,及其与高血压和平均血压昼夜变化(杓型现象)的关联。:开展了一项横断面研究,纳入118例诊断为T1D的青少年,对其进行临床和实验室检查、基因分析以及24小时动态血压监测。比较了高血压青少年与血压正常青少年的基因型频率。此外,还比较了杓型血压者与非杓型血压者的基因型频率。:高血压患者更可能为女性,血糖控制明显较差,甘油三酯水平较高,体重指数和每日胰岛素剂量增加。高血压组中基因型的患病率为II型20%、ID型66.7%、DD型13.3%,与血压正常组(II型29.1%、ID型53.4%、DD型17.5%)相比无显著差异( =0.625)。高血压组中基因型的患病率为AC型53.3%、AA型40%、CC型6.7%,与血压正常组(AC型39.8%、AA型52.4%、CC型7.8%)相比也无显著差异( =0.608)。共有46%的患者出现非杓型现象。基因型中,非杓型血压者的患病率为DD型13%、II型33.3%、ID型53.7%( =0.369),而基因型中,非杓型血压者的患病率为AA型50%、AC型42.6%、CC型7.4%( =0.976)。:我们的结果表明,在我们的T1D青少年患者中,较高的体重指数、甘油三酯、血糖控制欠佳以及女性性别等临床和代谢因素比和基因多态性更能预示高血压的发生。这一发现的一个潜在原因可能是患者年龄较小或研究组规模相对较小。需要开展涉及更大样本量的未来研究,以进一步调查高血压发生的遗传易感性。

相似文献

本文引用的文献

4
Prevalence of Hypertension in Children.儿童高血压患病率。
Hypertension. 2019 Jan;73(1):148-152. doi: 10.1161/HYPERTENSIONAHA.118.11673.
5
Familial aggregation and childhood blood pressure.家族聚集性与儿童血压
Curr Hypertens Rep. 2015 Jan;17(1):509. doi: 10.1007/s11906-014-0509-x.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验