印尼1型糖尿病患者CTLA-4 CT-60 A/G和CTLA-4 1822 C/T基因多态性

IF 2.6 Q2 GENETICS & HEREDITY
N. Rochmah, M. Faizi, Suhasta Nova, R. A. Setyoningrum, S. Basuki, A. Endaryanto
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In the control group, the inclusion criteria were healthy children, aged 4–18 years and willing to join this study. The exclusion criteria included children with ongoing infection, history of other autoimmune diseases, allergies, or malignancy. Results The mean age was 12.48 years old, and the mean of T1DM onset was 9.28 years old. The CTLA-4 1822 T allele observed in 62% T1DM and 56% in control (p = 0.388, OR = 0.78, 95% CI = 0.44–1.37) and CTLA-4 CT-60 G allele observed in 52% T1DM and 58% in control (p = 0.393, OR = 1.27, 95% CI = 0.73–2.22). The C/T genotypes was significantly higher in control group (p = 0.045, OR = 3.27, 95% CI = 1.00–10.62). The A/G genotypes was commonly found in control group (p = 0.765, OR = 1.20, 95% CI = 0.37–3.86). The Javanese was the dominant ethnic group in our study. Conclusion The frequency of CTLA-4 CT-60 A/G polymorphism almost equivalent in T1DM and control group. 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引用次数: 2

摘要

CTLA-4基因多态性在儿童1型糖尿病(T1DM)中起重要作用。然而,关于这一主题的数据在不同的种族和民族之间有所不同。目的分析T1DM患儿CTLA-4 CT-60 A/G和CTLA-4 1822 C/T基因与对照组的多态性。患者与方法采用聚合酶链反应-限制性片段长度多态性对25例T1DM患儿和25例对照组的CTLA-4 CT-60 A/G和CTLA-4 1822 C/T基因多态性进行分析。纳入标准是在Dr. Soetomo医院儿科内分泌门诊定期对照、年龄4-18岁且愿意加入本研究的患者,排除标准是在儿科重症监护室住院的T1DM患者。对照组的纳入标准为4-18岁的健康儿童,并自愿加入本研究。排除标准包括持续感染、其他自身免疫性疾病、过敏史或恶性肿瘤的儿童。结果患者平均年龄12.48岁,T1DM发病年龄9.28岁。CTLA-4 1822 T等位基因在T1DM患者中占62%,对照组中占56% (p = 0.388, OR = 0.78, 95% CI = 0.44-1.37), CTLA-4 CT-60 G等位基因在T1DM患者中占52%,对照组中占58% (p = 0.393, OR = 1.27, 95% CI = 0.73-2.22)。对照组C/T基因型差异有统计学意义(p = 0.045, OR = 3.27, 95% CI = 1.00-10.62)。对照组A/G基因型较多(p = 0.765, OR = 1.20, 95% CI = 0.37 ~ 3.86)。爪哇人是我们研究中的主要族群。结论CTLA-4 CT-60 A/G多态性在T1DM组与对照组的频率基本相当。而CTLA-4 1822 C/T多态性在对照组中更为普遍;因此,该基因型可能对T1DM具有保护作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CTLA-4 CT-60 A/G and CTLA-4 1822 C/T Gene Polymorphisms in Indonesians with Type 1 Diabetes Mellitus
Introduction CTLA-4 gene polymorphism plays an important role in children with type 1 diabetes mellitus (T1DM). However, data on this subject vary among different races and ethnics. Purpose To analyze CTLA-4 CT-60 A/G and CTLA-4 1822 C/T gene polymorphism among children with T1DM compared to control. Patients and Methods The CTLA-4 CT-60 A/G and CTLA-4 1822 C/T gene polymorphism in children with T1DM using polymerase chain reaction-restriction fragment length polymorphism in 25 T1DM and 25 controls. The inclusion criteria were patients regularly controlled at the Pediatric Endocrine Outpatient Clinic of Dr. Soetomo Hospital, aged 4–18 years and willing to join this study and the exclusion criteria were T1DM patients hospitalized in the pediatric intensive care unit. In the control group, the inclusion criteria were healthy children, aged 4–18 years and willing to join this study. The exclusion criteria included children with ongoing infection, history of other autoimmune diseases, allergies, or malignancy. Results The mean age was 12.48 years old, and the mean of T1DM onset was 9.28 years old. The CTLA-4 1822 T allele observed in 62% T1DM and 56% in control (p = 0.388, OR = 0.78, 95% CI = 0.44–1.37) and CTLA-4 CT-60 G allele observed in 52% T1DM and 58% in control (p = 0.393, OR = 1.27, 95% CI = 0.73–2.22). The C/T genotypes was significantly higher in control group (p = 0.045, OR = 3.27, 95% CI = 1.00–10.62). The A/G genotypes was commonly found in control group (p = 0.765, OR = 1.20, 95% CI = 0.37–3.86). The Javanese was the dominant ethnic group in our study. Conclusion The frequency of CTLA-4 CT-60 A/G polymorphism almost equivalent in T1DM and control group. However, CTLA-4 1822 C/T polymorphism was more prevalent in the control group; thus, this genotype may have a protective effect against T1DM.
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来源期刊
Application of Clinical Genetics
Application of Clinical Genetics Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
5.40
自引率
0.00%
发文量
20
审稿时长
16 weeks
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