Decreased mitochondrial DNA content in peripheral blood precedes the development of non-insulin-dependent diabetes mellitus

被引:180
作者
Lee, HK [1 ]
Song, JH
Shin, CS
Park, DJ
Park, KS
Lee, KU
Koh, CS
机构
[1] Seoul Natl Univ, Coll Med, Dept Internal Med, Seoul 110744, South Korea
[2] Natl Inst Hlth, Dept Biomed Sci, Eunpyung Ku, Seoul 122020, South Korea
[3] Univ Ulsan, Coll Med, Dept Internal Med, Seoul, South Korea
基金
美国国家科学基金会;
关键词
mitochondrial DNA; peripheral blood; non-insulin-dependent diabetes mellitus; waist-to-hip ratio; blood pressure; insulin resistance; pre-diabetes;
D O I
10.1016/S0168-8227(98)00110-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Qualitative changes in mitochondrial DNA (mtDNA), such as mutations and deletions, have been implicated in the pathogenesis of diabetes mellitus. In addition to the qualitative changes, mtDNA is subject to quantitative changes, and is vulnerable to oxidative stress, resulting in both qualitative and quantitative changes. This study was performed to investigate whether quantitative changes in mtDNA occur in non-insulin-dependent diabetes mellitus (NIDDM) patients and also in pre-diabetic subjects. MtDNA content from peripheral blood was measured by slot-blot analysis in 55 NIDDM patients and 29 age- and sex-matched control subjects. We have also analysed the mtDNA copies by quantitative polymerase chain reaction (PCR) method in 23 pre-diabetic subjects who converted to diabetic in 2 years and 12 age- and sex-matched control subjects who remained non-diabetic. Mean mtDNA quantity measured by slot blot method was 35% lower in patients with NIDDM than in control subjects (12.3 +/- 8.1 vs. 19.1 +/- 8.2 AU/mu g DNA; P < 0.05). MtDNA quantities did not correlate with age, body mass index, duration of diabetes or HbA(1c) levels. We have also found that the mtDNA copies in subjects who converted to diabetes in 2 years were lower than in controls even before the development of diabetes (102.8 +/- 41.5 vs. 137.8 +/- 67.7 copies/pg template DNA P(0.05). Inverse correlations were noted between mtDNA content and baseline waist hip circumference ratio (WHR) (r = -0.31, P < 0.05), and fasting glucose level (r = -0.35, P < 0.05), diastolic blood pressure (r = -0.36, P < 0.05), and WHR (r = -0.40, P < 0.01) after development of diabetes. In conclusion, we demonstrate that the content of mtDNA decreases in peripheral blood of patients with NIDDM and the lower mtDNA levels precede the development of diabetes. (C) 1998 Published by Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:161 / 167
页数:7
相关论文
共 21 条
[1]   MATERNALLY INHERITED DIABETES-MELLITUS - THE ROLE OF MITOCHONDRIAL-DNA DEFECTS [J].
ALCOLADO, JC ;
THOMAS, AW .
DIABETIC MEDICINE, 1995, 12 (02) :102-108
[2]   INCREASED EXPRESSION OF MITOCHONDRIAL-ENCODED GENES IN SKELETAL-MUSCLE OF HUMANS WITH DIABETES-MELLITUS [J].
ANTONETTI, DA ;
REYNET, C ;
KAHN, CR .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (03) :1383-1388
[3]   MATERNALLY TRANSMITTED DIABETES AND DEAFNESS ASSOCIATED WITH A 10.4 KB MITOCHONDRIAL-DNA DELETION [J].
BALLINGER, SW ;
SHOFFNER, JM ;
HEDAYA, EV ;
TROUNCE, I ;
POLAK, MA ;
KOONTZ, DA ;
WALLACE, DC .
NATURE GENETICS, 1992, 1 (01) :11-15
[4]   QUANTITATIVE PCR - VALIDATION OF THE USE OF A MULTISPECIFIC INTERNAL CONTROL [J].
COTTREZ, F ;
AURIAULT, C ;
CAPRON, A ;
GROUX, H .
NUCLEIC ACIDS RESEARCH, 1994, 22 (13) :2712-2713
[5]   MITOCHONDRIAL DIABETES-MELLITUS - A REVIEW [J].
GERBITZ, KD ;
VANDENOUWELAND, JMW ;
MAASSEN, JA ;
JAKSCH, M .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 1995, 1271 (01) :253-260
[6]   TYPE-2 (ON-INSULIN-DEPENDENT) DIABETES-MELLITUS - THE THRIFTY PHENOTYPE HYPOTHESIS [J].
HALES, CN ;
BARKER, DJP .
DIABETOLOGIA, 1992, 35 (07) :595-601
[7]   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
[8]   DIABETES-MELLITUS CARRYING A MUTATION IN THE MITOCHONDRIAL TRNA(LEU(UUR)) GENE [J].
KISHIMOTO, M ;
HASHIRAMOTO, M ;
ARAKI, S ;
ISHIDA, Y ;
KAZUMI, T ;
KANDA, F ;
KASUGA, M .
DIABETOLOGIA, 1995, 38 (02) :193-200
[9]   Oxidant-mediated repression of mitochondrial transcription in diabetic rats [J].
Kristal, BS ;
Koopmans, SJ ;
Jackson, CT ;
Ikeno, Y ;
Park, BJ ;
Yu, BP .
FREE RADICAL BIOLOGY AND MEDICINE, 1997, 22 (05) :813-822
[10]   Molecular genetic aspects of human mitochondrial disorders [J].
Larsson, NG ;
Clayton, DA .
ANNUAL REVIEW OF GENETICS, 1995, 29 :151-178