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Epidemiologic investigations of amyotrophic lateral sclerosis. 2. Familial aggregations indicative of dominant inheritance. II.肌萎缩侧索硬化症的流行病学调查。2. 提示显性遗传的家族聚集性。II.
Neurology. 1955 Apr;5(4):249-68. doi: 10.1212/wnl.5.4.249.
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Twin study using mortality data: a new sampling method.使用死亡率数据的双胞胎研究:一种新的抽样方法。
Int J Epidemiol. 1995 Aug;24(4):758-62. doi: 10.1093/ije/24.4.758.
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Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis.铜锌超氧化物歧化酶基因突变与家族性肌萎缩侧索硬化症相关。
Nature. 1993 Mar 4;362(6415):59-62. doi: 10.1038/362059a0.
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Human genetics. Did radicals strike Lou Gehrig?人类遗传学。是自由基侵袭了卢·格里克吗?
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The British Isles survey of multiple sclerosis in twins.英国双胞胎多发性硬化症调查。
Neurology. 1994 Jan;44(1):11-5. doi: 10.1212/wnl.44.1.11.
6
Cu/Zn superoxide dismutase (SOD1) mutations and sporadic amyotrophic lateral sclerosis.铜/锌超氧化物歧化酶(SOD1)突变与散发性肌萎缩侧索硬化症
Lancet. 1993 Oct 23;342(8878):1050-1. doi: 10.1016/0140-6736(93)92905-9.
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Twin studies in medical research.医学研究中的双胞胎研究。
Lancet. 1993 May 29;341(8857):1419.
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Twin studies in medical research.医学研究中的双胞胎研究。
Lancet. 1993 May 29;341(8857):1418-9.
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Twin studies in medical research.医学研究中的双胞胎研究。
Lancet. 1993 May 29;341(8857):1418.
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Twin studies in medical research: can they tell us whether diseases are genetically determined?医学研究中的双胞胎研究:它们能告诉我们疾病是否由基因决定吗?
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英国运动神经元病双胞胎研究。

British motor neuron disease twin study.

作者信息

Graham A J, Macdonald A M, Hawkes C H

机构信息

Clinical Neurology Department, The Ipswich Hospital NHS Trust, UK.

出版信息

J Neurol Neurosurg Psychiatry. 1997 Jun;62(6):562-9. doi: 10.1136/jnnp.62.6.562.

DOI:10.1136/jnnp.62.6.562
PMID:9219739
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1074137/
Abstract

OBJECTIVES

To investigate the cause of sporadic motor neuron disease (MND) by twin study, so allowing (1) estimation of the genetic contribution, and (2) collection of matched pairs for a case-control study of possible environmental factors.

METHODS

10872 death certificates bearing the diagnosis MND were collected from 1979 to 1989 inclusive. Inspection of individual birth entries allowed identification of potential twins. The status of each co-twin was determined and contact made through the National Health Service Central Register (NHS-CR) and their general practitioner (GP). The diagnosis of MND was verified via the co-twin and relatives, and medical records where available. Zygosity was assessed using a recognised questionnaire. Details concerning environmental exposures and health were gathered by interview of cotwin and relatives using a semistructured questionnaire. Heritability (h2) of MND was estimated, and the environmental information was analysed by conditional logistic regression modelling.

RESULTS

Seventy seven probands were identified, of whom 26 were monozygotic and 51 dizygotic. Four monozygotic probands were concordant, but two probands came from a family known to have familial MND. The estimated heritability was between 0.38 and 0.85. Most environmental risk factors were not significant. Regular vehicle maintenance (odds ratio (OR) = 7.0; 95% confidence interval (95% CI) 1.3-89.9) and occupational paint usage (OR = 3.75; 95% CI 1.0-17.1), however, occurred significantly more often in the affected cases.

CONCLUSIONS

This "death discordant" method for twin collection has proved to be viable, and has allowed the ascertainment of a large population sample in a rare disease. The genetic role in sporadic MND is substantial, and higher than expected. Exposure to industrial chemicals, particularly constituents of petrochemicals and paints, may contribute to the aetiology of MND.

摘要

目的

通过双胞胎研究调查散发性运动神经元病(MND)的病因,从而(1)估计遗传因素的作用,以及(2)收集匹配的双胞胎对,用于可能的环境因素的病例对照研究。

方法

收集了1979年至1989年(含)期间10872份诊断为MND的死亡证明。检查个人出生记录以识别潜在的双胞胎。确定每个双胞胎的状况,并通过国家卫生服务中央登记处(NHS-CR)及其全科医生(GP)进行联系。通过双胞胎和亲属以及现有病历核实MND的诊断。使用公认的问卷评估合子性。通过使用半结构化问卷对双胞胎和亲属进行访谈,收集有关环境暴露和健康的详细信息。估计MND的遗传率(h2),并通过条件逻辑回归模型分析环境信息。

结果

确定了77名先证者,其中26对为单卵双胞胎,51对为双卵双胞胎。4对单卵双胞胎先证者一致,但其中2名先证者来自一个已知有家族性MND的家庭。估计的遗传率在0.38至0.85之间。大多数环境风险因素不显著。然而,定期进行车辆维护(优势比(OR)=7.0;95%置信区间(95%CI)1.3-89.9)和职业性使用油漆(OR=3.75;95%CI 1.0-17.1)在患病病例中出现的频率明显更高。

结论

这种“死亡不一致”的双胞胎收集方法已被证明是可行的,并使得在罕见病中确定了大量人群样本。遗传因素在散发性MND中起重要作用,且比预期的更高。接触工业化学品,特别是石化产品和油漆的成分,可能有助于MND的病因学研究。