The age modification to leukocyte telomere length effect on bone mineral density and osteoporosis among Chinese elderly women

被引:15
作者
Tao, Lailin [1 ]
Huang, Qin [2 ]
Yang, Rui [3 ]
Dai, Yu [4 ]
Zeng, Yun [5 ]
Li, Can [1 ]
Li, Xiaolong [1 ]
Zeng, Junchao [3 ]
Wang, Qi [1 ]
机构
[1] Huazhong Univ Sci & Technol, Dept Epidemiol & Biostat, MOE Key Lab Environm & Hlth, Sch Publ Hlth,Tongji Med Coll, Wuhan 430030, Hubei, Peoples R China
[2] Huazhong Univ Sci & Technol, Dept Rehabil Med, Union Hosp, Tongji Med Coll, Wuhan 430030, Hubei, Peoples R China
[3] Huazhong Univ Sci & Technol, Union Hosp, Tongji Med Coll, Dept Hlth Checkup, Wuhan 430030, Hubei, Peoples R China
[4] Huazhong Univ Sci & Technol, Union Hosp, Tongji Med Coll, Dept Nucl Med, Wuhan 430030, Hubei, Peoples R China
[5] Wuhan 1 Hosp, Wuhan 430030, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
Bone mineral density; Osteoporosis; Telomere length; Elderly population; Aging; LIFE-SPAN; ASSOCIATION; FRACTURE; ESTROGEN; PERSPECTIVE; DIAGNOSIS; HEALTH; MODEL; TIME; MEN;
D O I
10.1007/s00774-019-01004-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Critically short telomeres indicate cellular senescence. Leukocyte telomere length (LTL) is regarded as an aging predictor. Osteoporosis is an age-related disease. The purpose of our study is to examine the association between LTL, and BMD and osteoporosis among an elderly Chinese population. A total of 1017 participants (584 postmenopausal women) with a mean age of 66.4 years were recruited from April 2016 to August 2017. Dual-energy X-ray absorptiometry was used for BMD measurement at skeleton sites of lumbar spine (LS), femoral neck (FN), and total hip (TH). LTL was measured using quantitative real-time polymerase chain reaction. Among women, age significantly modified the effect of LTL on BMD at FN. Additionally, significant age modification was observed for the association between LTL and LS BMD category (indicative of control or osteopenia or osteoporosis), and the number of osteoporotic sites at LS or TH. The corresponding estimates (95% CI) for the relative excess risk due to interaction (RERI) were - 0.07 (- 0.11, - 0.01) and - 0.11 (- 0.16, - 0.03) sequentially in ordinal logistic regression models. The estimated RERIs (95% CI) were - 0.11 (- 0.25, - 0.02) and - 0.23 (- 0.39, - 0.10) in multinomial logistic regression models for LS/FN/TH BMD category, and - 0.20 (- 0.31, - 0.09) and - 0.34 (- 0.49, - 0.21) for FN BMD category. However, similar findings did not show in men. The effect of LTL on BMD and osteoporosis risk is modified by age in elderly women but not in men, suggesting that the predictive role of LTL in bone loss differs by sex.
引用
收藏
页码:1004 / 1012
页数:9
相关论文
共 43 条
[1]  
[Anonymous], 2008, Modern epidemiology
[2]   Sex differences in telomeres and lifespan [J].
Barrett, Emma L. B. ;
Richardson, David S. .
AGING CELL, 2011, 10 (06) :913-921
[3]   Telomere length versus hormonal and bone mineral status in healthy elderly men [J].
Bekaert, S ;
Van Pottelbergh, I ;
De Meyer, T ;
Zmierczak, H ;
Kaufman, JM ;
Van Oostveldt, P ;
Goemaere, S .
MECHANISMS OF AGEING AND DEVELOPMENT, 2005, 126 (10) :1115-1122
[4]   STRUCTURE AND FUNCTION OF TELOMERES [J].
BLACKBURN, EH .
NATURE, 1991, 350 (6319) :569-573
[5]   CHRONIC CONDITIONS THAT LEAD TO FUNCTIONAL LIMITATION IN THE ELDERLY [J].
BOULT, C ;
KANE, RL ;
LOUIS, TA ;
BOULT, L ;
MCCAFFREY, D .
JOURNALS OF GERONTOLOGY, 1994, 49 (01) :M28-M36
[6]   Effects of estrogen plus progestin on risk of fracture and bone mineral density - The Women's Health Initiative randomized trial [J].
Cauley, JA ;
Robbins, J ;
Chen, Z ;
Cummings, SR ;
Jackson, RD ;
LaCroix, AZ ;
LeBoff, M ;
Lewis, CE ;
McGowan, J ;
Neuner, J ;
Pettinger, M ;
Stefanick, ML ;
Wactawski-Wende, J ;
Watts, NB .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2003, 290 (13) :1729-1738
[7]   Telomere measurement by quantitative PCR [J].
Cawthon, RM .
NUCLEIC ACIDS RESEARCH, 2002, 30 (10) :e47
[8]   The association between physical activity in leisure time and leukocyte telomere length [J].
Cherkas, Lynn F. ;
Hunkin, Janice L. ;
Kato, Bernet S. ;
Richards, J. Brent ;
Gardner, Jeffrey P. ;
Surdulescu, Gabriela L. ;
Kimura, Masayuki ;
Lu, Xiaobin ;
Spector, Tim D. ;
Aviv, Abraham .
ARCHIVES OF INTERNAL MEDICINE, 2008, 168 (02) :154-158
[9]   Identification of seven loci affecting mean telomere length and their association with disease [J].
Codd, Veryan ;
Nelson, Christopher P. ;
Albrecht, Eva ;
Mangino, Massimo ;
Deelen, Joris ;
Buxton, Jessica L. ;
Hottenga, Jouke Jan ;
Fischer, Krista ;
Esko, Tonu ;
Surakka, Ida ;
Broer, Linda ;
Nyholt, Dale R. ;
Leach, Irene Mateo ;
Salo, Perttu ;
Hagg, Sara ;
Matthews, Mary K. ;
Palmen, Jutta ;
Norata, Giuseppe D. ;
O'Reilly, Paul F. ;
Saleheen, Danish ;
Amin, Najaf ;
Balmforth, Anthony J. ;
Beekman, Marian ;
de Boer, Rudolf A. ;
Bohringer, Stefan ;
Braund, Peter S. ;
Burton, Paul R. ;
de Craen, Anton J. M. ;
Denniff, Matthew ;
Dong, Yanbin ;
Douroudis, Konstantinos ;
Dubinina, Elena ;
Eriksson, Johan G. ;
Garlaschelli, Katia ;
Guo, Dehuang ;
Hartikainen, Anna-Liisa ;
Henders, Anjali K. ;
Houwing-Duistermaat, Jeanine J. ;
Kananen, Laura ;
Karssen, Lennart C. ;
Kettunen, Johannes ;
Klopp, Norman ;
Lagou, Vasiliki ;
van Leeuwen, Elisabeth M. ;
Madden, Pamela A. ;
Maegi, Reedik ;
Magnusson, Patrik K. E. ;
Mannisto, Satu ;
McCarthy, Mark I. ;
Medland, Sarah E. .
NATURE GENETICS, 2013, 45 (04) :422-427
[10]   Insulin resistance, oxidative stress, hypertension, and leukocyte telomere length in men from the Framingham Heart Study [J].
Demissie, S. ;
Levy, D. ;
Benjamin, E. J. ;
Cupples, L. A. ;
Gardner, J. P. ;
Herbert, A. ;
Kimura, M. ;
Larson, M. G. ;
Meigs, J. B. ;
Keaney, J. F. ;
Aviv, A. .
AGING CELL, 2006, 5 (04) :325-330