Shortened telomere length in white blood cells of patients with IDDM

被引:181
作者
Jeanclos, E
Krolewski, A
Skurnick, J
Kimura, M
Aviv, H
Warram, JH
Aviv, A
机构
[1] Univ Med & Dent New Jersey, New Jersey Med Sch, Hypertens Res Ctr, Ctr Human & Mol Genet, Newark, NJ 07103 USA
[2] Univ Med & Dent New Jersey, New Jersey Med Sch, Dept Prevent Med & Community Hlth, Newark, NJ 07103 USA
[3] Harvard Univ, Sch Med, Joslin Diabet Ctr, Sect Epidemiol & Genet, Boston, MA 02115 USA
关键词
D O I
10.2337/diabetes.47.3.482
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IDDM is a polygenic and autoimmune disorder in which subsets of white blood cells (WBCs) are engaged in the destruction of beta-cells of the pancreas, The mechanisms that account for the abnormal behavior of these cells in IDDM are not fully understood, By measuring the mean length of telomeres of WBCs from patients with IDDM, we tested the concept that telomeres might play a role in IDDM. We examined the lengths of the terminal restriction fragments (TRFs) of DNA of WBCs from 234 white men comprising 54 patients with IDDM, 74 patients with NIDDM, and 106 control subjects, When adjusted for age, the TRP length from WBCs of patients with IDDM was significantly shorter than that of nondiabetic control subjects (mean +/- SE: 8.6 +/- 0.1 vs, 9.2 +/- 0.1, P = 0.002), No significant difference was observed between the TRF length from WBCs of patients with NIDDM versus nondiabetic subjects, Neither the duration nor the complications of IDDM (i,e,, nephropathy and hypertension) had apr effect on the TRF length of WBCs from patients with IDDM. The shortened TRF length of WBCs of patients with IDDM likely reflects a marked reduction in the TRF length of subsets of WBCs that play a role in the pathogenesis of IDDM.
引用
收藏
页码:482 / 486
页数:5
相关论文
共 24 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]   Of telomeres and tumors [J].
Axelrod, N .
NATURE MEDICINE, 1996, 2 (02) :158-159
[4]   TELOMERASE ACTIVITY IN NORMAL AND MALIGNANT HEMATOPOIETIC-CELLS [J].
BROCCOLI, D ;
YOUNG, JW ;
DELANGE, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (20) :9082-9086
[5]  
Chiu CP, 1997, P SOC EXP BIOL MED, V214, P99
[6]   Shortened telomeres in the expanded CD28- CD8+ cell subset in HIV disease implicate replicative senescence in HIV pathogenesis [J].
Effros, RB ;
Allsopp, R ;
Chiu, CP ;
Hausner, MA ;
Hirji, K ;
Wang, LL ;
Harley, CB ;
Villeponteau, B ;
West, MD ;
Giorgi, JV .
AIDS, 1996, 10 (08) :F17-F22
[7]   Mouse and man: Multiple genes and multiple autoantigens in the aetiology of type I DM and related autoimmune disorders [J].
Gottlieb, PA ;
Eisenbarth, GS .
JOURNAL OF AUTOIMMUNITY, 1996, 9 (02) :277-281
[8]   Telomere length regulation [J].
Greider, CW .
ANNUAL REVIEW OF BIOCHEMISTRY, 1996, 65 :337-365
[9]   TELOMERES SHORTEN DURING AGING OF HUMAN FIBROBLASTS [J].
HARLEY, CB ;
FUTCHER, AB ;
GREIDER, CW .
NATURE, 1990, 345 (6274) :458-460
[10]  
Hiyama E, 1996, INT J ONCOL, V9, P453