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.
引用
收藏
页码:1019 / 1023
页数:5
相关论文
共 50 条
  • [41] Novel mitochondrial tRNA(Leu(UUR)) gene mutations associated with diabetes in Japan.
    Hinokio, Y
    Suzuki, S
    Toyota, T
    DIABETES, 1996, 45 : 838 - 838
  • [42] Mitochondrial diabetes associated with tRNA Leu (UUR) mutation at position 3271 and two times of GAD antibody negative conversion
    Suzuki, Yoshihiko
    Irie, Junichiro
    Sano, Motoaki
    Kawai, Toshihide
    Meguro, Shu
    Ikemura, Nobuhiro
    DIABETES RESEARCH AND CLINICAL PRACTICE, 2016, 120 : S77 - S78
  • [43] β-Cell function in individuals carrying the mitochondrial tRNA Leu (UUR) mutation
    Salles, Joao Eduardo
    Kasamatsu, Teresa S.
    Dib, Sergio A.
    Moises, Regina S.
    PANCREAS, 2007, 34 (01) : 133 - 137
  • [44] INSULIN SENSITIVITY IN PATIENTS WITH NIDDM AND THE A-TO-G MUTATION AT NUCLEOTIDE-3,243 OF THE MITOCHONDRIAL TRNA(LEU(UUR)) GENE
    IWASAKI, N
    WASADA, T
    TAKAHASHI, Y
    BABAZONO, T
    OHGAWARA, H
    OMORI, Y
    DIABETES CARE, 1995, 18 (06) : 886 - 888
  • [45] The A to G transition at nt 3243 of the mitochondrial tRNA(Leu)(UUR) may cause an MERRF syndrome
    Fabrizi, GM
    Cardaioli, E
    Grieco, GS
    Cavallaro, T
    Malandrini, A
    Manneschi, L
    Dotti, MT
    Federico, A
    Guazzi, G
    JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1996, 61 (01): : 47 - 51
  • [46] GAD antibody in mitochondrial diabetes associated with tRNA(UUR) mutation at position 3271
    Suzuki, Y
    Taniyama, M
    Shimada, A
    Atumi, Y
    Matsuoka, K
    Oka, Y
    DIABETES CARE, 2002, 25 (06) : 1097 - 1098
  • [47] MATERNALLY INHERITED DIABETES AND DEAFNESS (MIDD) - A DISTINCT SUBTYPE OF DIABETES-ASSOCIATED WITH A MITOCHONDRIAL TRNA(LEU(UUR)) GENE POINT MUTATION
    VANDENOUWELAND, JMW
    LEMKES, HHPJ
    GERBITZ, KD
    MAASSEN, JA
    MUSCLE & NERVE, 1995, : S124 - S130
  • [48] A new mitochondrial DNA mutation associated with mitochondrial myopathy: tRNA(Leu(UUR)) 3254C-to-G
    Kawarai, T
    Kawakami, H
    Kozuka, K
    Izumi, Y
    Matsuyama, Z
    Watanabe, C
    Kohriyama, T
    Nakamura, S
    NEUROLOGY, 1997, 49 (02) : 598 - 600
  • [49] beta-cell loss and glucose induced signalling defects in diabetes mellitus caused by mitochondrial tRNA(Leu)(UUR) gene mutation
    Oka, Y
    Katagiri, H
    Ishihara, H
    Asano, T
    Kobayashi, T
    Kikuchi, M
    DIABETIC MEDICINE, 1996, 13 (09) : S98 - S102
  • [50] The mitochondrial tRNALeu(UUR) A to G 3243 mutation is associated with insulin-dependent and non-insulin-dependent diabetes in a Chinese population
    Smith, PR
    Dronsfield, MJ
    Mijovic, CH
    Hattersley, AT
    Yeung, VTF
    Cockram, C
    Chan, JCN
    Barnett, AH
    Bain, SC
    DIABETIC MEDICINE, 1997, 14 (12) : 1026 - 1031