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基因在女性单纯性甲状腺肿病因中的主要作用:一项基于人群的双胞胎研究。

Major role of genes in the etiology of simple goiter in females: a population-based twin study.

作者信息

Brix T H, Kyvik K O, Hegedüs L

机构信息

Department of Endocrinology M, Odense University Hospital, Odense University, Odense C, Denmark.

出版信息

J Clin Endocrinol Metab. 1999 Sep;84(9):3071-5. doi: 10.1210/jcem.84.9.5958.

Abstract

The etiology of simple goiter, affecting up to 5% of a population in nonendemic areas, is incompletely understood. It is generally believed to be multifactorial in origin, but the relative contributions of genetic and environmental factors remain to be clarified. Therefore, we investigated a well defined population of Danish twins. We performed a historical cohort study of 5.479 same sex twin pairs born between 1953 and 1972. Information on goiter was obtained from a nationwide questionnaire survey in 1994. Information from hospitals, out-patient clinics, and the subjects' general practitioners was sought to verify the diagnoses. Concordance rates, tetrachoric correlations, and heritability were determined. The crude probandwise concordance rates were 0.42 [95% confidence interval (CI), 0.26-0.591 and 0.13 (95% CI, 0.06-0.24) for female monozygotic and female dizygotic pairs, respectively. The age-adjusted cumulative probandwise risk for simple goiter from birth to age 43 yr was 0.53 (95% CI, 0.23-0.83) for female monozygotic twins and 0.18 (95% CI, 0.05-0.35) for female dizygotic twins (P = 0.003). The tetrachoric correlations were substantially higher in monozygotic (0.82; SE, 0.07) than in dizygotic twins (0.47; SE, 0.12). Model-fitting analysis suggested that the heritability of the liability to the development of simple goiter in women is approximately 82%. Individual-specific environmental factors not shared by cotwins seemed to explain the remaining 18%. We conclude that the etiology of clinically overt simple goiter is multifactorial. Genetic factors play a major role in the etiology of simple goiter in females, but environmental factors are also of importance.

摘要

单纯性甲状腺肿在非地方性流行地区影响着高达5%的人群,其病因尚未完全明确。一般认为其起源是多因素的,但遗传和环境因素的相对作用仍有待阐明。因此,我们对丹麦双胞胎这一明确界定的人群进行了研究。我们对1953年至1972年间出生的5479对同性双胞胎进行了一项历史性队列研究。甲状腺肿信息来自1994年的一项全国性问卷调查。我们从医院、门诊诊所及受试者的全科医生处获取信息以核实诊断。确定了一致性率、四分相关系数和遗传度。女性单卵双胞胎和女性双卵双胞胎的粗先证者一致性率分别为0.42[95%置信区间(CI),0.26 - 0.59]和0.13(95%CI,0.06 - 0.24)。女性单卵双胞胎从出生到43岁时单纯性甲状腺肿的年龄调整累积先证者风险为0.53(95%CI,0.23 - 0.83),女性双卵双胞胎为0.18(95%CI,0.05 - 0.35)(P = 0.003)。四分相关系数在单卵双胞胎(0.82;标准误,0.07)中显著高于双卵双胞胎(0.47;标准误,0.12)。模型拟合分析表明,女性发生单纯性甲状腺肿易感性的遗传度约为82%。双胞胎未共享的个体特异性环境因素似乎解释了其余的18%。我们得出结论,临床显性单纯性甲状腺肿的病因是多因素的。遗传因素在女性单纯性甲状腺肿的病因中起主要作用,但环境因素也很重要。

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