Arthus Marie-Françoise, Lonergan Michèle, Crumley M Joyce, Naumova Anna K, Morin Denis, DE Marco Luiz A, Kaplan Bernard S, Robertson Gary L, Sasaki Sei, Morgan Kenneth, Bichet Daniel G, Fujiwara T Mary
Department of Medicine, Université de Montréal and Research Centre, Hôpital du Sacré-Coeur de Montréal, Montreal, Canada.
Montreal General Hospital Research Institute, Montreal, Canada.
J Am Soc Nephrol. 2000 Jun;11(6):1044-1054. doi: 10.1681/ASN.V1161044.
X-linked nephrogenic diabetes insipidus (NDI) is a rare disease caused by mutations in the arginine vasopressin receptor 2 gene (AVPR2). Thirty-three novel AVPR2 mutations were identified in 62 families that were not included in our previous studies. This study describes the diversity of mutations observed in a total of 117 families, the number of affected people at the time of diagnosis, skewed X chromosome inactivation in severely affected females, the inferred parental origin of de novo mutations, and it provides estimates of incidence. Among 117 families, there were 82 different putative disease-causing mutations. Based on haplotype analysis, it can be inferred that when the same AVPR2 mutation is identified in different families that were not known to be related, the mutations most likely arose independently. More than half of the families had only one affected male; two families presented with a severely affected female and no family history of NDI. A de novo mutation arose during oogenesis in the mother in 20% of isolated cases. The estimate of about 8.8 per million male live births of the incidence of X-linked NDI in the province of Quebec, Canada may be representative of the general population except in Nova Scotia and New Brunswick, where the incidence is more than six times higher. Documentation of the diversity of mutations will assist in revealing the full spectrum of clinical variation. Discussion of genetic and population genetic aspects of X-linked NDI may contribute to early diagnosis and treatment.
X连锁肾性尿崩症(NDI)是一种由精氨酸加压素受体2基因(AVPR2)突变引起的罕见疾病。在我们之前的研究未纳入的62个家庭中鉴定出33种新的AVPR2突变。本研究描述了在总共117个家庭中观察到的突变多样性、诊断时受影响的人数、严重受影响女性中X染色体失活的偏倚、新发突变的推断亲本来源,并提供了发病率估计。在117个家庭中,有82种不同的假定致病突变。基于单倍型分析,可以推断,当在未知相关的不同家庭中鉴定出相同的AVPR2突变时,这些突变很可能是独立出现的。超过一半的家庭只有一名受影响的男性;两个家庭中有一名严重受影响的女性,且无NDI家族史。在20%的散发病例中,新发突变发生在母亲的卵子发生过程中。加拿大魁北克省X连锁NDI发病率约为每百万男性活产8.8例,这一估计可能代表除新斯科舍省和新不伦瑞克省以外的一般人群,在这两个省份发病率高出六倍多。记录突变的多样性将有助于揭示临床变异的全貌。对X连锁NDI的遗传和群体遗传方面的讨论可能有助于早期诊断和治疗。