High basal metabolic rate is a risk factor for mortality: The Baltimore Longitudinal Study of Aging

被引:110
作者
Ruggiero, Carmelinda [1 ,4 ]
Metter, E. Jeffrey [1 ]
Melenovsky, Vojtech [2 ]
Cherubini, Antonio [4 ]
Najjar, Samer S. [3 ]
Ble, Alessandro [1 ]
Senin, Umberto [4 ]
Longo, Dan L. [1 ]
Ferrucci, Luigi [1 ]
机构
[1] NIA, Longitudinal Studies Sect, Clin Res Branch, NIH, Baltimore, MD 21224 USA
[2] Inst Clin & Expt Med IKEM, Dept Cardiol, Prague, Czech Republic
[3] NIA, NIH, Human Cardiovasc Studies Unit, Lab Cardiovasc Sci, Baltimore, MD 21225 USA
[4] Univ Perugia, Sch Med, Dept Clin & Expt Med, Inst Gerontol & Geriatr, I-06100 Perugia, Italy
来源
JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES | 2008年 / 63卷 / 07期
关键词
basal metabolic rate; metabolism; mortality; longevity; theory of aging; aging;
D O I
10.1093/gerona/63.7.698
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Background. Despite longstanding controversies from animal studies on the relationship between basal metabolic rate (BMR) and longevity, whether BMR is a risk factor for mortality has never been tested in humans. We evaluate the longitudinal changes in BMR and the relationship between BMR and mortality in the Baltimore Longitudinal Study of Aging (BLSA) participants. Methods. BMR and medical information were collected at the study entry and approximately every 2 years in 1227 participants (972 men) over a 40-year follow-up. BMR, expressed as kcal/m(2)/h, was estimated from the basal O-2 consumption and CO2 production measured by open-circuit method. Data on all-cause and specific-cause mortality were also obtained. Result. BMR declined with age at a rate that accelerated at older ages. Independent of age. participants who died had a higher BMR compared to those who survived. BMR was a significant risk factor for mortality independent of secular trends in mortality and other well-recognized risk factors for mortality, such as age, body mass index, smoking, white blood cell count, and diabetes. BMR was nonlinearly associated with mortality. The lowest mortality rate was found in the BMR range 31.3-33.9 kcal/m(2)/h. Participants with BMR in the range 33.9-36.4 kcal/m(2)/h and above the threshold of 36.4 kcal/m(2)/h experienced 28% (hazard ratio: 1.28; 95% confidence interval, 1.02-1.61) and 53% (hazard ratio: 1.53; 95% confidence interval, 1.19-1.96) higher mortality risk compared to participants with BMR 31.3-33.9 kcal/m2/h. Conclusion. We confirm previous findings of an age-related decline of BMR. In our study, a blunted age-related decline in BMR was associated with higher mortality, suggesting that such condition reflects poor health status.
引用
收藏
页码:698 / 706
页数:9
相关论文
共 38 条
[1]   COMPENDIUM OF PHYSICAL ACTIVITIES - CLASSIFICATION OF ENERGY COSTS OF HUMAN PHYSICAL ACTIVITIES [J].
AINSWORTH, BE ;
HASKELL, WL ;
LEON, AS ;
JACOBS, DR ;
MONTOYE, HJ ;
SALLIS, JF ;
PAFFENBARGER, RS .
MEDICINE AND SCIENCE IN SPORTS AND EXERCISE, 1993, 25 (01) :71-80
[2]  
[Anonymous], PUBLICATION CARNEGIE
[3]  
[Anonymous], 1932, Quantitative Clinical Chemistry
[4]   The free radical theory of aging matures [J].
Beckman, KB ;
Ames, BN .
PHYSIOLOGICAL REVIEWS, 1998, 78 (02) :547-581
[5]  
Bodkin NL, 2003, J GERONTOL A-BIOL, V58, P212
[6]   A network-based analysis of systemic inflammation in humans [J].
Calvano, SE ;
Xiao, WZ ;
Richards, DR ;
Felciano, RM ;
Baker, HV ;
Cho, RJ ;
Chen, RO ;
Brownstein, BH ;
Cobb, JP ;
Tschoeke, SK ;
Miller-Graziano, C ;
Moldawer, LL ;
Mindrinos, MN ;
Davis, RW ;
Tompkins, RG ;
Lowry, SF .
NATURE, 2005, 437 (7061) :1032-1037
[7]   THE THEORETICAL BASES OF INDIRECT CALORIMETRY - A REVIEW [J].
FERRANNINI, E .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1988, 37 (03) :287-301
[8]   The origins of age-related proinflammatory state [J].
Ferrucci, L ;
Corsi, A ;
Lauretani, F ;
Bandinelli, S ;
Bartali, B ;
Taub, DD ;
Guralnik, JM ;
Longo, DL .
BLOOD, 2005, 105 (06) :2294-2299
[9]  
HARE RS, 1950, P SOC EXP BIOL MED, V74, P148
[10]   AGING - A THEORY BASED ON FREE-RADICAL AND RADIATION-CHEMISTRY [J].
HARMAN, D .
JOURNALS OF GERONTOLOGY, 1956, 11 (03) :298-300