Eur J Endocrinol
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


DOI: 10.1530/eje.1.02308
European Journal of Endocrinology, Vol 156, Issue 1, 83-90
Copyright © 2007 by European Society of Endocrinology
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (2)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Hovind, P.
Right arrow Articles by Janssen, J. A M J L
Right arrow Search for Related Content
PubMed
Right arrow Articles by Hovind, P.
Right arrow Articles by Janssen, J. A M J L

CLINICAL STUDY

An IGF-I gene polymorphism modifies the risk of developing persistent microalbuminuria in type 1 diabetes

Peter Hovind1,4, Steven Lamberts2, Wim Hop3, Jaap Deinum2, Lise Tarnow1, Hans-Henrik Parving1 and Joop A M J L Janssen2

1 Steno Diabetes Center, Gentofte, Denmark, 2 Departments of Internal Medicine and 3 Epidemiology and Biostatistics, Erasmus MC, Room D-436, s-Gravendijkwal, 230 3015 CE Rotterdam, The Netherlands and 4 Department of Clinical Physiology and Nuclear Medicine, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark

(Correspondence should be addressed to J A M J L Janssen; Email: j.a.m.j.l.janssen{at}erasmusmc.nl)

Objective: Derangements of the GH–IGF-I axis have been associated with microalbuminuria (MA) in type 1 diabetes. The aim of this study was to investigate whether an IGF-I gene promoter polymorphism influenced the development of persistent MA in type 1 diabetes.

Design: A prospective follow-up study of a cohort of 277 patients with newly diagnosed type 1 diabetes consecutively enrolled between September 1979 and August 1984.

Methods: Urinary albumin excretion rate over 24 h was measured in each patient at least once a year. Persistent MA was defined as a urinary albumin excretion rate between 30 and 300 mg/24 h.

Results: During a median follow-up of 18.0 years (range 1.0–21.5), 79 of 277 patients developed persistent MA. IGF-I gene genotype was available for 216 subjects; in 73% of the subjects, the wild-type genotype of this IGF-I gene polymorphism was present, while 27% had the variant type. At baseline, there were no differences in IGF-I levels and HbA1c values between subjects with the wild type and subjects with variant type. By Kaplan–Meier analysis, subjects with the variant type of this polymorphism had during follow-up a higher risk of development of MA compared subjects with the wild type (P = 0.03).

Conclusions: Subjects with the variant type of an IGF-I gene polymorphism had a significantly increased risk of developing MA. This risk was not mediated through changes in circulating IGF-I levels. Our study suggests that in type 1 diabetes, this IGF-I gene polymorphism is a risk factor of MA.




This article has been cited by other articles:


Home page
Diabetes CareHome page
A. Morimoto, R. Nishimura, T. Matsudaira, H. Sano, N. Tajima, and for the Diabetes Epidemiology Research Internation
Is Pubertal Onset a Risk Factor for Blindness and Renal Replacement Therapy in Childhood-Onset Type 1 Diabetes in Japan?
Diabetes Care, September 1, 2007; 30(9): 2338 - 2340.
[Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2007 European Society of Endocrinology.