Telomere shortening of peripheral blood mononuclear cells in coronary disease patients with metabolic disorders

被引:50
作者
Obana, N
Takagi, S
Kinouchi, Y
Tokita, Y
Sekikawa, A
Takahashi, S
Hiwatashi, N
Oikawa, S
Shimosegawa, T
机构
[1] Tohoku Univ, Postgrad Med Sch, Dept Gastroenterol, Aoba Ku, Sendai, Miyagi 9808574, Japan
[2] Tohoku Univ, Postgrad Med Sch, Dept Mol Metab & Diabet, Aoba Ku, Sendai, Miyagi 9808574, Japan
[3] Nippon Med Coll, Dept Med, Div Endocrinol Diabet & Metab, Tokyo 113, Japan
关键词
telomere; coronary diseases; hypercholesterolemia; diabetes mellitus;
D O I
10.2169/internalmedicine.42.150
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective Telomere shortening is correlated with cell turnover and aging, but it has been recently suggested to occur not only by aging but by several biochemical factors of metabolic disorders predisposing to atherosclerosis. Patients and Methods We compared telomere length of peripheral blood mononuclear cells of patients with the metabolic disorders, hypercholesterolemia (HC) and diabetes mellitus (DM), according to the presence or absence of coronary diseases. Results The results demonstrated that HC and/or DM patients with coronary diseases have significantly shorter telomere length than healthy controls (p=0.0014). Conclusion Telomere shortening may be involved in the mechanisms that promote coronary diseases under some circumstances of metabolic disorders.
引用
收藏
页码:150 / 153
页数:4
相关论文
共 23 条
[1]   TELOMERE LENGTH PREDICTS REPLICATIVE CAPACITY OF HUMAN FIBROBLASTS [J].
ALLSOPP, RC ;
VAZIRI, H ;
PATTERSON, C ;
GOLDSTEIN, S ;
YOUNGLAI, EV ;
FUTCHER, AB ;
GREIDER, CW ;
HARLEY, CB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (21) :10114-10118
[2]   Reflections on telomeres, growth, aging, and essential hypertension [J].
Aviv, A ;
Aviv, H .
HYPERTENSION, 1997, 29 (05) :1067-1072
[3]   STRUCTURE AND FUNCTION OF TELOMERES [J].
BLACKBURN, EH .
NATURE, 1991, 350 (6319) :569-573
[4]   GENE-EXPRESSION IN QUIESCENT AND SENESCENT FIBROBLASTS [J].
CAMPISI, J .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES-SERIES, 1992, 663 :195-201
[5]   TELOMERE LENGTH AND REPLICATIVE AGING IN HUMAN VASCULAR TISSUES [J].
CHANG, E ;
HARLEY, CB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (24) :11190-11194
[6]   Age-dependent telomere shortening is slowed down by enrichment of intracellular vitamin C via suppression of oxidative stress [J].
Furumoto, K ;
Inoue, E ;
Nagao, N ;
Hiyama, E ;
Miwa, N .
LIFE SCIENCES, 1998, 63 (11) :935-948
[7]   TELOMERES SHORTEN DURING AGING OF HUMAN FIBROBLASTS [J].
HARLEY, CB ;
FUTCHER, AB ;
GREIDER, CW .
NATURE, 1990, 345 (6274) :458-460
[8]   TELOMERE REDUCTION IN HUMAN COLORECTAL-CARCINOMA AND WITH AGING [J].
HASTIE, ND ;
DEMPSTER, M ;
DUNLOP, MG ;
THOMPSON, AM ;
GREEN, DK ;
ALLSHIRE, RC .
NATURE, 1990, 346 (6287) :866-868
[9]   Shortened telomere length in white blood cells of patients with IDDM [J].
Jeanclos, E ;
Krolewski, A ;
Skurnick, J ;
Kimura, M ;
Aviv, H ;
Warram, JH ;
Aviv, A .
DIABETES, 1998, 47 (03) :482-486
[10]  
Kinoshita M, 2000, CLIN CHEM, V46, P822