Age related alteration at pancreatic beta-cell function - Increased proinsulin and proinsulin-to-insulin molar ratio in elderly, but not in obese, subjects without glucose intolerance

被引:58
作者
Shimizu, M [1 ]
Kawazu, S [1 ]
Tomono, S [1 ]
Ohno, T [1 ]
Utsugi, T [1 ]
Kato, N [1 ]
Ishii, C [1 ]
Ito, Y [1 ]
Murata, K [1 ]
机构
[1] GUNMA UNIV,SCH MED,DEPT INTERNAL MED 2,MAEBASHI,GUMMA 371,JAPAN
关键词
D O I
10.2337/diacare.19.1.8
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
OBJECTIVE - To determine the secretion of insulin, C-peptide, and proinsulin after oral glucose loading in healthy elderly subjects compared with middle-aged subjects with and without obesity and with NIDDM. RESEARCH DESIGN AND METHODS - Subjects fell into four groups: nonobese middle-aged normal control subjects (CNT group; n = 38, 40-64 years old); obese normal subjects (OB group; n = 18, 40-64 years old); nonobese NIDDM subjects (NIDDM group; n = 28, 40-64 years old); and nonobese elderly subjects (OL group; n = 17, 65-92 years old). Insulin, C-peptide, and proinsulin were determined by radioimmunoassay in plasma samples taken at 0, 30, 60, and 120 min during a 75-g oral glucose tolerance test (OGTT). RESULTS - There were no differences in plasma glucose during the OGTT among the three nondiabetic groups. Hyperinsulinemia was significant in the OB and NIDDM groups but not in the OL group. On the other hand, absolute hyperproinsulinemia was significant in the OL and NIDDM groups compared with the CNT group. Increased proinsulin was rather dominant in the OL group, especially late after glucose loading. Molar ratios of proinsulin to insulin or C-peptide thus were significantly higher in the OL and NIDDM groups. CONCLUSIONS - Alteration of pancreatic beta-cell function independent of that seen with NIDDM occurred in relation to aging. This may be a predisposing factor to the development of impaired glucose tolerance or NIDDM in elderly subjects, that is, independent of obesity.
引用
收藏
页码:8 / 11
页数:4
相关论文
共 16 条
[1]
INSULIN DEFICIENCY AND INCREASED PLASMA-CONCENTRATION OF INTACT AND 32/33 SPLIT PROINSULIN IN SUBJECTS WITH IMPAIRED GLUCOSE-TOLERANCE [J].
DAVIES, MJ ;
RAYMAN, G ;
GRAY, IP ;
DAY, JL ;
HALES, CN .
DIABETIC MEDICINE, 1993, 10 (04) :313-320
[2]
EFFECTS OF AGING ON INSULIN-SECRETION [J].
GUMBINER, B ;
POLONSKY, KS ;
BELTZ, WF ;
WALLACE, P ;
BRECHTEL, G ;
FINK, RI .
DIABETES, 1989, 38 (12) :1549-1556
[3]
PREVALENCE OF DIABETES AND IMPAIRED GLUCOSE-TOLERANCE AND PLASMA-GLUCOSE LEVELS IN UNITED-STATES POPULATION AGED 20-74 YR [J].
HARRIS, MI ;
HADDEN, WC ;
KNOWLER, WC ;
BENNETT, PH .
DIABETES, 1987, 36 (04) :523-534
[4]
PREPARATION OF IODINE-131 LABELLED HUMAN GROWTH HORMONE OF HIGH SPECIFIC ACTIVITY [J].
HUNTER, WM ;
GREENWOOD, FC .
NATURE, 1962, 194 (4827) :495-&
[5]
INSULIN RESPONSES IN EQUIVOCAL AND DEFINITE DIABETES, WITH SPECIAL REFERENCE TO SUBJECTS WHO HAD MILD GLUCOSE-INTOLERANCE BUT LATER DEVELOPED DEFINITE DIABETES [J].
KOSAKA, K ;
HAGURA, R ;
KUZUYA, T .
DIABETES, 1977, 26 (10) :944-952
[6]
LEAKY JL, 1992, DIABETES CARE, V15, P442
[7]
ALTERATIONS IN IMMUNOREACTIVE PROINSULIN AND INSULIN-CLEARANCE INDUCED BY WEIGHT-LOSS IN NIDDM [J].
POLONSKY, KS ;
GUMBINER, B ;
OSTREGA, D ;
GRIVER, K ;
TAGER, H ;
HENRY, RR .
DIABETES, 1994, 43 (07) :871-877
[8]
HYPERPROINSULINEMIA AND AMYLOID IN NIDDM - CLUES TO ETIOLOGY OF ISLET BETA-CELL DYSFUNCTION [J].
PORTE, D ;
KAHN, SE .
DIABETES, 1989, 38 (11) :1333-1336
[9]
RAYMOND IF, 1983, J CLIN INVEST, V71, P1523
[10]
WHAT BETA-CELL DEFECT COULD LEAD TO HYPERPROINSULINEMIA IN NIDDM - SOME CLUES FROM RECENT ADVANCES MADE IN UNDERSTANDING THE PROINSULIN-PROCESSING MECHANISM [J].
RHODES, CJ ;
ALARCON, C .
DIABETES, 1994, 43 (04) :511-517