Brix T H, Christensen K, Holm N V, Harvald B, Hegedüs L
Department of Endocrinology (M), Odense University Hospital, Denmark.
Clin Endocrinol (Oxf). 1998 Apr;48(4):397-400. doi: 10.1046/j.1365-2265.1998.00450.x.
The aetiology of Graves' disease (GD) is generally thought to fit a multi-factorial pattern of inheritance in which clinical disease develops on the basis of genetic susceptibility interacting with environmental and endogenous factors. In previous twin studies the probandwise concordance rates for hyperthyroidism were as high as 0.86 in monozygotic twins and 0.20 in dizygotic twins, indicating a very strong genetic influence. In these studies, however, no effort was made to distinguish between GD and non-autoimmune hyperthyroidism, and one study also included patients with simple non-toxic goitre, hampering if not invalidating any conclusions. The aim of the present study was to determine whether there is a genetic contribution in the aetiology of GD.
Historical cohort study of pairs of same-sex twins, with information on GD being gathered by questionnaire surveys in the 1950s and 1960s. All available hospital material was sought to verify the diagnosis, which was assigned on the basis of clinical and histopathological evidence. The healthy co-twins were followed through middle age by questionnaire surveys in the 1970s and 1980s.
Same-sex twin individuals born between 1870-1920, included in a population-based nationwide register. A total of 118 subjects indicated hospitalization due to GD. A hospital record was available in 76 subjects. Of these, 55 (46 females and 9 males) could be classified as having GD.
Pairwise and probandwise concordance rates for GD in monozygotic and dizygotic twin pairs.
The probandwise concordance rates were 0.36 for monozygotic pairs and 0 for dizygotic pairs. The pairwise concordance rates were 0.22 and 0 for monozygotic and dizygotic pairs, respectively. The concordance rates were significantly (P = 0.012) higher in monozygotic than in dizygotic pairs.
These results confirm that genetic factors play an important role in the aetiology of Graves' disease. However, they may not be as powerful as previously thought.
一般认为格雷夫斯病(GD)的病因符合多因素遗传模式,即临床疾病是在遗传易感性与环境及内源性因素相互作用的基础上发展而来。在以往的双胞胎研究中,单卵双胞胎中甲状腺功能亢进的先证者一致率高达0.86,双卵双胞胎中为0.20,表明遗传影响非常强烈。然而,在这些研究中,未努力区分GD和非自身免疫性甲状腺功能亢进,且一项研究还纳入了单纯性非毒性甲状腺肿患者,这即便没有使任何结论无效,也妨碍了结论的得出。本研究的目的是确定GD病因中是否存在遗传因素。
对同性双胞胎对进行历史性队列研究,通过20世纪50年代和60年代的问卷调查收集有关GD的信息。寻求所有可用的医院资料以核实诊断,诊断基于临床和组织病理学证据。通过20世纪70年代和80年代的问卷调查对健康的双胞胎进行中年随访。
1870年至1920年出生的同性双胞胎个体,纳入基于人群的全国登记册。共有118名受试者因GD住院。76名受试者有医院记录。其中,55名(46名女性和9名男性)可归类为患有GD。
单卵和双卵双胞胎对中GD的成对和先证者一致率。
单卵双胞胎对的先证者一致率为0.36,双卵双胞胎对为0。单卵和双卵双胞胎对的成对一致率分别为0.22和0。单卵双胞胎对的一致率显著高于双卵双胞胎对(P = 0.012)。
这些结果证实遗传因素在格雷夫斯病的病因中起重要作用。然而,它们可能不如先前认为的那么强大。