Neonatal diabetes mellitus:: Chromosomal analysis in transient and permanent cases

被引:73
作者
Metz, C
Cavé, H
Bertrand, AM
Deffert, C
Gueguen-Giroux, B
Czernichow, P
Polak, M
机构
[1] Hop Robert Debre, INSERM Unite 457, Serv Endocrinol & Diabetol Pediat, F-75019 Paris, France
[2] Hop Robert Debre, Pediat Endocrine Unit, F-75019 Paris, France
[3] Hosp Morvan, Dept Pediat, Brest, France
[4] CHU Besancon, Dept Pediat, F-25030 Besancon, France
关键词
D O I
10.1067/mpd.2002.127089
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Objectives: To describe a large cohort of patients with transient neonatal diabetes mellitus TNDM) and permanent neonatal diabetes mellitus (PNDM), and to investigate whether chromosome 6 analysis helps to distinguish TNDM from PNDM. Study design: Patients with TNDM (n = 29) (insulin therapy for <3,ears) and 21 with PNDM were identified through a nationwide study. Results: Although patients with PNDM were less likely to have had intrauterine growth restriction (36% vs 74% for TNDM, P < .006), were older at diagnosis (median: 27 vs 6 clays, P < .01), and had higher initial insulin requirements (1.4 U/kg/day vs 0.6 U/kg/day, P < .006), no clinical features were reliable in distinguishing PNDM from TNDM on an individual case basis. Permanent insulin-dependent diabetes developed in 5 TNDM patients after 8 years of age, emphasizing the need For prolonged follow-up. Among the 19 TNDM patients tested. two had paternal isodisomy of chromosome 6, seven from 4 families had paternally-derived trisomy of the 6q region, and two had a methylation defect in the 6q24 region. No chromosome 6 anomalies were found in the 9 PNDM patients tested. Conclusion: When present, a chromosome 6 abnormality is strongly in favor of the "transient" form of the disease.
引用
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页码:483 / 489
页数:7
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