GENETIC-BASIS OF ENDOCRINE DISEASE .1. MOLECULAR-GENETICS OF INSULIN RESISTANT DIABETES-MELLITUS

被引:59
作者
TAYLOR, SI
CAMA, A
ACCILI, D
BARBETTI, F
IMANO, E
KADOWAKI, H
KADOWAKI, T
机构
[1] UNIV TOKYO, FAC MED, DEPT INTERNAL MED 3, TOKYO 113, JAPAN
[2] ASAHI LIFE FDN, INST DIABET CARE & RES, TOKYO, JAPAN
[3] OSAKA UNIV, DEPT INTERNAL MED 1, OSAKA, JAPAN
关键词
D O I
10.1210/jcem-73-6-1158
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
GENETIC factors are an important determinant of whether an individual will develop noninsulindependent diabetes mellitus (NIDDM). However, the pattern of inheritance of NIDDM is complex and not well understood. In fact, the genetic complexity led one author to refer to diabetes mellitus as a “geneticist’s nightmare” (1). Nevertheless, the pathophysiology of the disease is becoming better understood. Most patients with NIDDM are resistant to the biological actions of insulin (2, 3). Prospective studies have demonstrated that insulin resistance is a prominent feature early in the natural history of the disease when the patients have impaired glucose tolerance, even before the time that they develop overt diabetes. Whether or not an insulin resistant patient develops NIDDM is determined by the capacity of the pancreatic β-cell to secrete sufficient insulin to overcome the insulin resistance (2-4). In those patients who develop insulin deficiency in addition to insulin resistance, the level of plasma glucose rises and the patient develops diabetes mellitus. © 1991 by The Endocrine Society.
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页码:1158 / 1163
页数:6
相关论文
共 31 条
[1]  
ACCILI D, 1991, J BIOL CHEM, V266, P434
[2]   A MUTATION IN THE INSULIN-RECEPTOR GENE THAT IMPAIRS TRANSPORT OF THE RECEPTOR TO THE PLASMA-MEMBRANE AND CAUSES INSULIN-RESISTANT DIABETES [J].
ACCILI, D ;
FRAPIER, C ;
MOSTHAF, L ;
MCKEON, C ;
ELBEIN, SC ;
PERMUTT, MA ;
RAMOS, E ;
LANDER, E ;
ULLRICH, A ;
TAYLOR, SI .
EMBO JOURNAL, 1989, 8 (09) :2509-2517
[3]   GENE FOR NON-INSULIN-DEPENDENT DIABETES-MELLITUS (MATURITY-ONSET DIABETES OF THE YOUNG SUBTYPE) IS LINKED TO DNA POLYMORPHISM ON HUMAN CHROMOSOME-20Q [J].
BELL, GI ;
XIANG, KS ;
NEWMAN, MV ;
WU, SH ;
WRIGHT, LG ;
FAJANS, SS ;
SPIELMAN, RS ;
COX, NJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (04) :1484-1488
[4]   A MUTATION IN THE TYROSINE KINASE DOMAIN OF THE INSULIN-RECEPTOR ASSOCIATED WITH INSULIN RESISTANCE IN AN OBESE WOMAN [J].
CAMA, A ;
SIERRA, MDLL ;
OTTINI, L ;
KADOWAKI, T ;
GORDEN, P ;
IMPERATOMCGINLEY, J ;
TAYLOR, SI .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1991, 73 (04) :894-901
[5]   THE AMINO-ACID-SEQUENCE OF THE INSULIN-RECEPTOR IS NORMAL IN AN INSULIN-RESISTANT PIMA INDIAN [J].
CAMA, A ;
PATTERSON, AP ;
KADOWAKI, T ;
KADOWAKI, H ;
SIEGEL, G ;
DAMBROSIO, D ;
LILLIOJA, S ;
ROTH, J ;
TAYLOR, SI .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1990, 70 (04) :1155-1161
[6]   THE TRIUMVIRATE - BETA-CELL, MUSCLE, LIVER - A COLLUSION RESPONSIBLE FOR NIDDM [J].
DEFRONZO, RA .
DIABETES, 1988, 37 (06) :667-687
[7]  
DEPREZ RHL, 1989, DIABETOLOGIA, V32, P740
[8]   2 PATIENTS WITH INSULIN RESISTANCE DUE TO DECREASED LEVELS OF INSULIN-RECEPTOR MESSENGER-RNA [J].
IMANO, E ;
KADOWAKI, H ;
KADOWAKI, T ;
IWAMA, N ;
WATARAI, T ;
KAWAMORI, R ;
KAMADA, T ;
TAYLOR, SI .
DIABETES, 1991, 40 (05) :548-557
[9]  
KADOWAKI H, 1990, J BIOL CHEM, V265, P21285
[10]   A NONSENSE MUTATION CAUSING DECREASED LEVELS OF INSULIN-RECEPTOR MESSENGER-RNA - DETECTION BY A SIMPLIFIED TECHNIQUE FOR DIRECT SEQUENCING OF GENOMIC DNA AMPLIFIED BY THE POLYMERASE CHAIN-REACTION [J].
KADOWAKI, T ;
KADOWAKI, H ;
TAYLOR, SI .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (02) :658-662