Increased prevalence of imprinting defects in patients with Angelman syndrome born to subfertile couples

被引:213
作者
Ludwig, M
Katalinic, A
Gross, S
Sutcliffe, A
Varon, R
Horsthemke, B
机构
[1] Endokrinologikum Hamburg, Zentrum Hormone & Stoffwechselerkrankungen Gyneko, D-22767 Hamburg, Germany
[2] Univ Klinikum Essen, Inst Humangenet, Essen, Germany
[3] UCL, Dept Paediat, London WC1E 6BT, England
[4] Humboldt Univ, Charite, Inst Humangenet, D-1086 Berlin, Germany
关键词
D O I
10.1136/jmg.2004.026930
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Recent case reports have suggested that infertility treatment with intracytoplasmic sperm injection (ICSI) may increase the risk of imprinting defects leading to Angelman syndrome (AS). Although imprinting defects account for only 4% of patients with AS, we have found four cases among 16 AS patients born to subfertile couples, who conceived with or without infertility treatment (25%; relative risk (RR) 6.25; 95% confidence interval (CI) 1.68 to 16.00). The risk in untreated couples with time to pregnancy (TTP) exceeding 2 years was identical to that of those treated by ICSI or by hormonal stimulation alone (RR 6.25; 95% CI 0.70 to 22.57). It was twice as high in couples who had received treatment and also had TTP > 2 years (RR 12.5; 95% CI 1.40 to 45.13). Our findings suggest that imprinting defects and subfertility may have a common cause, and that superovulation rather than ICSI may further increase the risk of conceiving a child with an imprinting defect.
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页码:289 / 291
页数:3
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