Diabetes mellitus associated with the 3243 mitochondrial tRNA(Leu(UUR)) mutation: Insulin secretion and sensitivity

被引:23
作者
Suzuki, Y
Iizuka, T
Kobayashi, T
Nishikawa, T
Atsumi, Y
Kadowaki, T
Oka, Y
Kadowaki, H
Taniyama, M
Hosokawa, K
机构
[1] YOKOHAMA ROSAI HOSP, DEPT MED, YOKOHAMA, KANAGAWA, JAPAN
[2] TORANOMON GEN HOSP, DEPT ENDOCRINOL & METAB, TOKYO, JAPAN
[3] UNIV TOKYO, DEPT INTERNAL MED 3, TOKYO 113, JAPAN
[4] YAMAGUCHI UNIV, DEPT INTERNAL MED 3, YAMAGUCHI, JAPAN
[5] ASAHI LIFE FDN, INST DIABET CARE & RES, TOKYO, JAPAN
[6] SHOWA UNIV, DEPT INTERNAL MED 3, TOKYO, JAPAN
来源
METABOLISM-CLINICAL AND EXPERIMENTAL | 1997年 / 46卷 / 09期
关键词
D O I
10.1016/S0026-0495(97)90272-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To investigate the pathophysiology of diabetes mellitus associated with the 3243 mitochondrial tRNA(LeU(UUR)) mutation (DM-Mt3243), insulin secretion and sensitivity were studied using the 75-g oral glucose tolerance test (oGTT), l-mg intravenous glucagon test, and euglycemic glucose clamp test. Twelve DM-Mt3243 patients were investigated (seven men and five women). Their ages ranged from 36 to 74 years, and the onset of diabetes occurred at 44.5 +/- 9.5 years (mean +/- SD). In the glucose tolerance test, nine patients (75.0%) showed lower C-peptide reactivity (CPR) than normal at 30 minutes, suggesting blunted insulin secretion. Three patients showed an impaired glucose tolerance (IGT) pattern, although they had absolute hyperglycemia at the onset of diabetes. In the glucagon test, 10 patients (76.3%) had CPR within the normal range at 6 minutes, indicating an adequate response. In the glucose clamp test, the WI value was 8.70 +/- 2.35 mg/kg/min and was within normal limits in all patients. The glucose metabolized (Fn value) was negatively correlated with 24-hour urinary C-peptide excretion (r=.696, P<.05). Thus, plasma CPR to glucose loading was blunted in many DM-Mt3243 patients, but CPR to glucagon was relatively well preserved. This difference in the intrinsic insulin response to the two stimuli may be characteristic of DM-Mt3243. Although M values were normal in all subjects, the correlation with 24-hour urinary C-peptide excretion suggests a relationship between insulin sensitivity and insulin secretion. These two mechanisms may cooperate to maintain homeostasis in this disease. Since three patients did not progress with aging, this mutation may not always cause gradual beta-cell destruction. Copyright (C) 1997 by W.B. Saunders Company.
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收藏
页码:1019 / 1023
页数:5
相关论文
共 23 条
[1]  
[Anonymous], 1985, World Health Organ Tech Rep Ser, V727, P1
[2]  
FRIER BM, 1977, DIABETES, V26, P369
[3]  
IIZUKA T, 1994, J JPN DIABETES SOC S, V37, P255
[4]  
Iizuka Takashi, 1996, Endocrine Journal, V43, pS107, DOI 10.1507/endocrj.43.Suppl_S107
[5]   INSULIN SENSITIVITY IN PATIENTS WITH NIDDM AND THE A-TO-G MUTATION AT NUCLEOTIDE-3,243 OF THE MITOCHONDRIAL TRNA(LEU(UUR)) GENE [J].
IWASAKI, N ;
WASADA, T ;
TAKAHASHI, Y ;
BABAZONO, T ;
OHGAWARA, H ;
OMORI, Y .
DIABETES CARE, 1995, 18 (06) :886-888
[6]   LEBERS HEREDITARY OPTIC NEUROPATHY - CLINICAL MANIFESTATIONS OF THE 3460 MUTATION [J].
JOHNS, DR ;
SMITH, KH ;
MILLER, NR .
ARCHIVES OF OPHTHALMOLOGY, 1992, 110 (11) :1577-1581
[7]   MITOCHONDRIAL GENE MUTATION AND INSULIN-DEFICIENT TYPE OF DIABETES-MELLITUS [J].
KADOWAKI, H ;
TOBE, K ;
MORI, Y ;
SAKURA, H ;
SAKUTA, R ;
NONAKA, I ;
HAGURA, R ;
YAZAKI, Y ;
AKANUMA, Y ;
KADOWAKI, T .
LANCET, 1993, 341 (8849) :893-894
[8]   A SUBTYPE OF DIABETES-MELLITUS ASSOCIATED WITH A MUTATION OF MITOCHONDRIAL-DNA [J].
KADOWAKI, T ;
KADOWAKI, H ;
MORI, Y ;
TOBE, K ;
SAKUTA, R ;
SUZUKI, Y ;
TANABE, Y ;
SAKURA, H ;
AWATA, T ;
GOTO, Y ;
HAYAKAWA, T ;
MATSUOKA, K ;
KAWAMORI, R ;
KAMADA, T ;
HORAI, S ;
NONAKA, I ;
HAGURA, R ;
AKANUMA, Y ;
YAZAKI, Y .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 330 (14) :962-968
[9]   INSULIN-RESISTANCE IN MITOCHONDRIAL GENE MUTATION [J].
KANAMORI, A ;
TANAKA, K ;
UMEZAWA, S ;
MATOBA, K ;
FUJITA, Y ;
IIZUKA, T ;
YAJIMA, Y .
DIABETES CARE, 1994, 17 (07) :778-779
[10]   MITOCHONDRIAL DIABETES-MELLITUS - PREVALENCE AND CLINICAL CHARACTERIZATION OF DIABETES DUE TO MITOCHONDRIAL TRNA(LEU(UUR)) GENE MUTATION IN JAPANESE PATIENTS [J].
KATAGIRI, H ;
ASANO, T ;
ISHIHARA, H ;
INUKAI, K ;
ANAI, M ;
YAMANOUCHI, T ;
TSUKUDA, K ;
KIKUCHI, M ;
KITAOKA, H ;
OHSAWA, N ;
YAZAKI, Y ;
OKA, Y .
DIABETOLOGIA, 1994, 37 (05) :504-510