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. 2012 Mar 7;35(3):973–984. doi: 10.1007/s11357-012-9398-6

Fitness, fatness and survival in elderly populations

Jean Woo 1,3,, Ruby Yu 1, Forrest Yau 2
PMCID: PMC3636403  PMID: 22391688

Abstract

This study examines the relative importance of fitness versus fatness in predicting mortality in elderly populations aged 70 years and over, and whether fitness may account for the ‘paradoxical’ relationship between better survival and increasing weight. Four thousand community-living Chinese men and women aged 65 years or over were recruited and stratified so that approximately 33% were in each of the age groups: 65–69, 70–74, and 75 or above. Medical history, height, weight, waist–hip ratio, body composition using DEXA, and walking speed were obtained. They were followed up for a mean of 7.0 years to ascertain death. Compared with the high fitness category, those in the moderate and low categories have a 43% and 68% increased risk of mortality at 7 years adjusting for multiple confounders. When mortality risk according to various fatness indicators was examined, only the lowest quartile of BMI, BFI, and FLMR conferred statistically significant increased risk. Fitness categories were significantly associated with all fatness indicators. The finding of fewer people in the high fitness category among the highest quartiles of other fatness indicators suggests that fitness is not the underlying mechanism for the obesity paradox. Within each quartile of fatness indicator, there was a significant trend towards reduced mortality with increasing fitness. In conclusion, the study confirms the beneficial effects of cardiorespiratory fitness on mortality but does not explain the ‘obesity paradox’. The findings underscore the importance of maintaining physical fitness through exercise and re-confirm the importance of weight maintenance in reducing mortality risk.

Keywords: Body mass index, Body fat, Waist–hip ratio, Fitness, Mortality

Introduction

An inverse relationship between body mass index and mortality among elderly populations has been documented in several studies among diverse ethnic groups.

Values for body mass index that are considered overweight, as well as other fatness indicators considered to be related to adverse outcomes in the general adult population, appear to confer some survival benefits among elderly populations with mean age of 70–80 years (Auyeung et al. 2010; Flicker et al. 2010; Lee et al. 2011a, b; Stessman et al. 2009; Woo et al. 2001, 2002). Cardiorespiratory fitness has been shown to modulate the adverse health outcomes of obesity in terms of mortality, morbidity, and the development of cardiovascular risk factors (Fogelholm 2010). A review of 36 studies showed that outcomes for participants who were obese and fit were better compared with those with normal weight but were unfit (Fogelholm 2010). However, only two studies examined the elderly population prospectively among Caucasian population aged >60 years (McAuley et al. 2009; Sui et al. 2007), and the lowest mortality was observed in obese men with high fitness, suggesting that in studies of the relationship between fatness and mortality, cardiorespiratory fitness may be a major confounder (McAuley et al. 2010b).

Findings from a previous study using data from the Mr & Ms Os cohort of elderly Chinese aged 65 years and above showed that survival in older men may benefit from being slightly overweight and centrally obese (Auyeung et al. 2010). However, the role of cardiorespiratory fitness in modulating this relationship was not addressed. The relative importance of fitness versus fatness and any interaction between them in predicting adverse outcomes in elderly populations has not been examined. Addressing this question is important in guiding health promotion efforts among the elderly with respect to lifestyle goals. Furthermore, it would contribute to understanding the underlying mechanisms for the obesity paradox (McAuley et al. 2010a). These research questions were explored using available data from a large cohort study.

Methods

Four thousand community-living Chinese men and women aged 65 years or over were recruited for a cohort study on osteoporosis and general health in Hong Kong between August 2001 and December 2003. Recruitment was by notices in senior social centers and housing estates as a large proportion of the elderly population resides in housing estates and attends senior social centers. Talks were given to explain the purpose, procedures, and investigations to be carried out. We excluded those who were unable to walk independently, had bilateral hip replacements, were not competent to give informed consent, and had medical conditions (in the judgment of the study physicians) which made it unlikely that they would survive a follow-up period of at least 4 years. The sample was stratified so that approximately 33% were in each of the age groups: 65–69, 70–74, and 75 or above. The study was approved by the Clinical Research Ethics Committee of the Chinese University of Hong Kong. All participants gave written consent to allow their personal, psychosocial, and physical data thus obtained to be used for research purposes.

A questionnaire containing information regarding demographics and medical history was administered by trained interviewers. Smokers were classified by having ever smoked more than five packs of cigarettes in the past, smoking currently, or never smoked. Medical diagnoses were based on the subjects’ report of their physician’s diagnoses, supplemented by medications brought to the interviewers. Diabetes, heart disease, and cancer were defined by self-reporting (ever being told to have the condition by a physician). Heart disease included coronary heart disease, heart failure, and myocardial infarction. The number of medications was taken as the total number of medications the participants were taking at the time of the assessment and which they brought to the place of the assessment. The name of the medication was recorded and subsequently classified into broad groups by a medical doctor.

Body weight was measured, with subjects wearing a light dressing gown, by the Physician Balance Beam Scale (Health-O-Meter, Arlington Heights, IL, USA). Height was measured by the Holtain Harpenden stadiometer (Holtain Ltd, Crosswell, UK). Waist circumferences (the circumference around the trunk midway between the rib cage and the pelvis) and hip circumferences (the maximum circumference around the buttock posteriorly and the pubis symphysis anteriorly) were measured with a flexible measuring tape. Only one measurement was taken. Four research assistants were involved in the measurement of the waist and the hip. The inter-rater reliability intra-class correlation using 15 subjects was 0.985 and 0.879 for waist and hip circumference, respectively.

Body composition (total body muscle mass, total body fat mass, and truncal fit mass) was measured by DXA using Hologic Delphi W4500 (Hologic Delphi, auto whole body version 12.4, Hologic Inc, Bedford, MA, USA) at baseline. The upper border of the abdominal region was defined by a horizontal line drawn through the lower one-third of the vertical height between the left midpoint acromion and the external end of left iliac crest. The lower border of the abdominal region was defined by a horizontal line through the external ends of the iliac crests (adapted from Bertin et al. 2000). The abdominal height was reduced to the lower one-third instead of the lower half as in the report by Bertin et al. because the latter method would have included the lungs and heart due to the smaller body size in the Chinese population. We were not able to use the method of measuring abdominal fat as defined by the region between the L1 and L4 vertebrae because many subjects had scoliosis and low bone mass, making the delineation of the upper or lower borders of these vertebrae difficult from a whole-body DXA scan. The relative truncal fat (RTF) was calculated as the proportion of abdominal fat within whole body fat (RTF = truncal fat/whole body fat ×100%). The maximum coefficient of variation for fat is 1.47%. Body mass index (BMI) was calculated by dividing the weight in kilograms by height in square meters. Body fat index (BFI) was calculated as the total body fat mass divided by height in square meters. Fat to lean mass ratio (FLMR), an indicator of fat to muscle mass, was calculated by dividing the total body fat mass by the total body muscle mass. Two indicators of visceral obesity were used: waist to hip ratio (WHR) and relative truncal fat (RTF).

Walking speed was measured using the average time in seconds to complete a walk along a straight line 6 m long. A warm-up period of <5 min was followed by two walks, and the average time recorded. In this study we used this measure as an indicator of cardiorespiratory fitness (CF) as it is easier to incorporate in large cohort studies, compared with maximal oxygen uptake (VO2max) on treadmill or bicycle exercises. In a subgroup of the cohort during a subsequent follow-up, we measured VO2max values in 757 men and 488 women and noted a good age-adjusted correlation between walking speed and VO2max (ϒ = 0.43, P < 0.001) (Yau 2011). This correlation was comparable to another indicator of CF used in other studies, the distance walked over 6 min (ϒ = 0.51, P < 0.001) (Rolland et al. 2004; Simonsick et al. 2001). As we did not carry out the 6-min walk distance test at baseline but only measured the walking speed, the latter was used as a surrogate of CF.

After a mean follow-up period of 7.0 ± 1.3 years, death was ascertained from the Hong Kong government’s Death Registry in the Department of Health, with the cause of death classified according to the International Classification of Disease (ICD) version 10 codes.

Statistical analysis

Continuous variables are presented as mean ± SD and categorical variables as absolute and percentage. Descriptive statistics summarized baseline characteristics by BMI category. Subjects were also categorized based on their fitness (using walking speed as indicator, in meters per second) and fatness levels. Cox proportional hazards analyses were used to determine the associations of fitness category with time to death adjusting for age in years, sex, medical history (diabetes, stroke, hypertension, myocardial infarction, angina, and congestive heart failure), cardiovascular disease medications (angiotensin-converting enzyme inhibitors, aspirin, β-blockers, calcium channel blockers, and statins), current smoking, and BMI in kilograms per square meter, or other fatness indices (entered as continuous variables). The associations of each fatness index category with time to death were also determined by Cox proportional hazards analyses. For each fatness index, three multivariate models were undertaken, with the first model adjusting for age in years, sex, medical history, cardiovascular disease medications, and current smoking and the second model adjusting for the covariates included in model 1 with additional adjustment of fitness as a continuous variable, and the third model adjusting for the covariates included in model 2 with additional adjustment of the interaction term between each fatness index and fitness, e.g., BMI in kilograms per square meter × fitness in meters per second. Additionally, fitness–fatness groups were tested using chi-square tests, and the joint effects of fitness and fatness on time to death were determined by Cox proportional hazards analyses. Tests for linear trend in mortality across the fitness category of each fatness quartile were also obtained by using chi-square tests. All analyses were carried out using the Window-based SPSS statistical package (version 17.0; SPSS Inc., Chicago, IL), and P values less than 0.05 were considered statistically significant.

Results

The baseline characteristics of study participants are shown in Table 1. Compared with the high ambulatory capacity (high fitness) category, those in the moderate and low categories have a 43% and 68% increased risk of mortality at 7 years adjusting for multiple confounders (Table 2). When mortality risk according to various fatness indicators was examined, only the lowest quartile of BMI, BFI, and FLMR conferred statistically significant increased risk. The relationship with WHR, an indicator of visceral obesity, showed a U-shape relationship with mortality with the second quartile having the lowest risk. No association was observed with relative truncal fat (Table 3). These results were unchanged when fitness was added as a potential confounder (model 2, Table 3), suggesting that fatness and fitness have independent effects on mortality as a health outcome. Additional tests for interaction between fatness and fitness were not statistically significant (model 3, Table 3). However, fitness categories were significantly associated with all fatness indicators (Table 4). The association is generally inverse, with fewer people in the high fitness category among the highest quartiles of fatness indicators, the only exception being RTF. For the highest RTF quartile, there were more people in the high fitness category. The findings of fewer people in the high fitness category among the highest quartiles of other fatness indicators suggest that fitness is not the underlying mechanism for the obesity paradox.

Table 1.

Baseline characteristics of study participants

Variable BMI category
All (n = 4,000) Underweight Normal weight Overweight Obese
< 18.5 (n = 215) 18.5–24.9 (n = 2,471) 25.0–29.9 (n = 1,190) ≥ 30.0 (n = 124)
Demographics
 Age (years) 72.5 ± 5.2 74.7 ± 6.2 72.6 ± 5.3 72.0 ± 4.7 71.8 ± 4.5
Fatness indicators
 BMI (kg/m2) 23.7 ± 3.3 17.2 ± 1.1 22.3 ± 1.7 26.8 ± 1.3 31.9 ± 1.9
 BFI (kg/m2) 7.1 ± 2.4 3.3 ± 1.2 6.3 ± 1.6 8.8 ± 1.8 12.1 ± 2.1
 FLMR (kg/kg) 0.5 ± 0.2 0.3 ± 0.1 0.4 ± 0.1 0.5 ± 0.1 0.7 ± 0.2
 WHR (cm/cm) 0.9 ± 0.1 0.8 ± 0.1 0.9 ± 0.1 1.0 ± 0.1 1.0 ± .01
 RTF (kg/kg) 0.5 ± 0.1 0.5 ± 0.1 0.5 ± 0.1 0.6 ± 0.1 0.5 ± 0.0
Medical history
 Diabetes 579 (14.5) 9 (4.2) 341 (13.8) 204 (17.1) 25 (20.2)
 Stroke 175 (4.4) 8 (3.7) 111 (4.5) 53 (4.5) 3 (2.4)
 Hypertension 1,707 (42.7) 41 (19.1) 955 (38.6) 650 (54.6) 61 (49.2)
 Heart attack/coronary/myocardial infarction 393 (9.8) 7 (3.3) 217 (8.8) 149 (12.5) 20 (16.1)
 Angina (chest pain) 352 (8.8) 10 (4.7) 186 (7.5) 135 (11.3) 21 (16.9)
 Congestive heart failure/enlarged heart 151 (3.8) 7 (3.3) 78 (3.2) 62 (5.2) 4 (3.2)
 Current smoker 275 (6.9) 37 (17.2) 176 (7.1) 57 (4.8) 5 (4.0)
Medications
 ACE inhibitor 438 (11.0) 14 (6.5) 230 (9.3) 172 (14.5) 22 (17.7)
 Aspirin 446 (11.2) 13 (6.0) 253 (10.2) 162 (13.6) 18 (14.5)
 Beta blocker 647 (16.2) 6 (2.8) 341 (13.8) 269 (22.6) 31 (25.0)
 Calcium channel blocker 722 (18.1) 17 (7.9) 424 (17.2) 256 (21.5) 25 (20.2)
 HMG CoA reductase inhibitor (statin) 238 (6.0) 3 (1.4) 125 (5.1) 98 (8.2) 12 (9.7)
Clinical
 SBP (mm Hg) 142.6 ± 19.3 137.1 ± 21.3 142.0 ± 19.0 144.7 ± 19.0 145.1 ± 21.3
 DBP (mm Hg) 77.8 ± 9.2 74.8 ± 9.9 77.4 ± 9.2 78.9 ± 9.0 81.2 ± 8.5
Fitness (walking speed, m/s)a 0.97 ± 0.22 0.93 ± 0.25 0.98 ± 0.22 0.95 ± 0.21 0.89 ± 0.21
Fitness categoryb
 Low fitness 1,338 (33.5) 84 (39.1) 763 (30.9) 436 (36.6) 55 (44.4)
 Moderate fitness 1,339 (33.5) 63 (29.3) 823 (33.3) 414 (34.8) 39 (31.5)
 High fitness 1,323 (33.1) 68 (31.6) 885 (35.8) 340 (28.6) 30 (24.2)

Data are presented as mean ± SD or number (percentage)

ACE angiotensin-converting enzyme inhibitor, BFI body fat index, BMI body mass index, DBP diastolic blood pressure, FLMR fat–lean mass ratio, RTF relative truncal fat, SBP systolic blood pressure, WHR waist to hip ratio

aFitness was assessed with a 6-m walk test

bFitness was assessed with a 6-m walk test. Fitness tertiles: 1st, walking speed <0.88 m/s (low fitness); 2nd, walking speed 0.88– <1.05 m/s (moderate fitness); 3 rd, walking speed ≥1.05 m/s (high fitness)

Table 2.

Multivariate proportional mortality hazard ratios (HRs) by fitness category in study participants

Fitness categorya No. of subjects No. (%) of deaths HR (95% CI)
Model 1 Model 2 Model 3 Model 4 Model 5 Model 6
Low fitness 1,338 209 (15.6) 1.65 (1.30–2.10)** 1.66 (1.30–2.11)** 1.68 (1.32–2.14)** 1.68 (1.32–2.14)** 1.65 (1.29–2.10)** 1.61 (1.27–2.05)**
Moderate fitness 1,339 159 (11.9) 1.41 (1.11–1.80)** 1.43 (1.12–1.81)** 1.44 (1.13–1.83)** 1.44 (1.13–1.83)** 1.41 (1.11–1.80)** 1.41 (1.11–1.80)**
High fitness 1,323 119 (9.0) 1 (reference) 1 (reference) 1 (reference) 1 (reference) 1 (reference) 1 (reference)

Model 1, adjusted for age, sex, medical history (diabetes, stroke, hypertension, myocardial infarction, angina, and congestive heart failure), current smoking, and CVD medications (ACE inhibitor, aspirin, beta blocker, calcium channel blocker, and statin)

Model 2, adjusted for covariates listed in model 1 plus BMI (entered as a continuous variable in kilograms per square meter)

Model 3, adjusted for covariates listed in model 1 plus BFI (entered as a continuous variable in kilograms per square meter)

Model 4, adjusted for covariates listed in model 1 plus FLMR (entered as a continuous variable in kilograms per kilogram)

Model 5, adjusted for covariates listed in model 1 plus WHR (entered as a continuous variable in centimeters per centimeter)

Model 6, adjusted for covariates listed in model 1 plus RTF (entered as a continuous variable in kilograms per kilogram)

CI confidence interval

**P < 0.01

aFitness was assessed with a 6-m walk test. Fitness tertiles: 1st, walking speed <0.88 m/s (low fitness); 2nd, walking speed 0.88– <1.05 m/s (moderate fitness); 3 rd, walking speed ≥1.05 m/s (high fitness)

Table 3.

Multivariate proportional mortality hazard ratios (HRs) by fatness category in study participants

Fatness indicators No. of subjects No. (%) of deaths Model 1 Model 2 Model 3
HR (95% CI) P value HR (95% CI) P value HR (95% CI) P value P interaction
BMI
 1st quartile 1,000 168 (16.8) 1.63 (1.27–2.11) 0.000 1.63 (1.26–2.10) 0.000 1.37 (1.00–1.88) 0.049 0.066
 2nd quartile 1,000 96 (9.6) 1 (reference) 1 (reference) 1 (reference)
 3rd quartile 1,000 115 (11.5) 1.16 (0.88–1.52) 0.298 1.15 (0.88–1.51) 0.318 1.29 (0.95–1.73) 0.099
 4th quartile 1,000 108 (10.8) 1.20 (0.91–1.59) 0.192 1.16 (0.88–1.53) 0.299 1.53 (1.02–2.29) 0.038
BFI
 1st quartile 1,000 194 (19.4) 1.37 (0.99–1.88) 0.056 1.44 (1.05–1.99) 0.025 1.20 (0.66–2.19) 0.553 0.474
 2nd quartile 1,000 118 (11.8) 0.89 (0.64–1.23) 0.485 0.93 (0.67–1.29) 0.676 0.83 (0.52–1.31) 0.421
 3rd quartile 1,000 100 (10.0) 0.90 (0.66–1.23) 0.510 0.92 (0.67–1.26) 0.586 0.85 (0.59–1.24) 0.400
 4th quartile 1,000 75 (7.5) 1 (reference) 1 (reference) 1 (reference)
FLMR
 1st quartile 1,000 196 (19.6) 1.71 (1.16–2.52) 0.007 1.83 (1.24–2.69) 0.002 1.87 (0.96–3.65) 0.065 0.930
 2nd quartile 1,000 139 (13.9) 1.23 (0.84–1.80) 0.287 1.29 (0.88–1.88) 0.192 1.31 (0.78–2.21) 0.314
 3rd quartile 1,000 91 (9.1) 1.11 (0.78–1.56) 0.567 1.14 (0.81–1.60) 0.467 1.15 (0.76–1.72) 0.507
 4th quartile 1,000 61 (6.1) 1 (reference) 1 (reference) 1 (reference)
WHR
 1st quartile 997 124 (12.4) 1.50 (1.14–1.98) 0.004 1.50 (1.14–1.98) 0.004 1.60 (1.16–2.20) 0.004 0.459
 2nd quartile 962 86 (8.9) 1 (reference) 1 (reference) 1 (reference)
 3rd quartile 1,040 139 (13.4) 1.43 (1.09–1.87) 0.010 1.41 (1.08–1.85) 0.013 1.35 (1.01–1.81) 0.045
 4th quartile 1,000 138 (13.8) 1.42 (1.08–1.87) 0.012 1.34 (1.02–1.77) 0.036 1.21 (0.81–1.79) 0.358
RTF
 1st quartile 1,000 126 (12.6) 1.28 (0.99–1.67) 0.061 1.25 (0.96–1.62) 0.098 1.36 (0.98–1.88) 0.068 0.412
 2nd quartile 1,001 106 (10.6) 1 (reference) 1 (reference) 1 (reference)
 3rd quartile 999 125 (12.5) 0.93 (0.72–1.21) 0.606 0.93 (0.71–1.20) 0.565 0.88 (0.66–1.18) 0.384
 4th quartile 1,000 130 (13.0) 0.79 (0.60–1.03) 0.081 0.79 (0.60–1.03) 0.083 0.70 (0.46–1.04) 0.079

BMI quartiles: 1st, < 21.57; 2nd, 21.57– < 23.53; 3rd, 23.53– < 25.72; 4th, ≥ 25.72. BFI quartiles: 1st, < 5.41; 2nd, 5.41– < 6.88; 3rd, 6.88– < 8.59; 4th, ≥ 8.59. FLMR quartiles: 1st, < 0.34; 2nd, 0.34– < 0.43; 3rd, 0.43– < 0.56; 4th, ≥ 0.56. WHR quartiles: 1st, < 0.88; 2nd, 0.88– < 0.92; 3rd, 0.92– < 0.97; 4th, ≥ 0.97. RTF quartiles: 1st, < 0.50; 2nd, 0.50– < 0.54; 3rd, 0.54– < 0.58; 4th, ≥ 0.58

Model 1, adjusted for age, sex, medical history (diabetes, stroke, hypertension, myocardial infarction, angina, and congestive heart failure/enlarged heart), current smoking, and CVD medications (ACE inhibitor, aspirin, beta blocker, calcium channel blocker, and statin)

Model 2, adjusted for covariates listed in model 1 plus fitness, i.e., walking speed in meters per second (entered as a continuous variable)

Model 3, adjusted for covariates listed in model 2 plus the interaction term between each fatness index and fitness, e.g., BMI in kilograms per square meter × walking speed in meters per second

P interaction = P values for interaction between each fatness index and fitness in the Cox proportional hazard model

BFI body fat index, BMI body mass index, CI confidence interval, FLMR fat–lean mass ratio, RTF relative truncal fat, WHR waist to hip ratio

Table 4.

Fatness indices and fitness categories

Fitness categorya
Fatness index Low fitness (n = 1,338) Moderate fitness (n = 1,339) High fitness (n = 1,323) P value
BMI
 1st quartile 331 (24.7) 330 (24.6) 339 (25.6) 0.000
 2nd quartile 314 (23.5) 310 (23.2) 376 (28.4)
 3rd quartile 318 (23.8) 349 (26.1) 333 (25.2)
 4th quartile 375 (28.0) 350 (26.1) 275 (20.8)
BFI
 1st quartile 286 (21.4) 284 (21.2) 430 (32.5) 0.000
 2nd quartile 263 (19.7) 357 (26.7) 380 (28.7)
 3rd quartile 355 (26.5) 339 (25.3) 306 (23.1)
 4th quartile 434 (32.4) 359 (26.8) 207 (15.6)
FLMR
 1st quartile 265 (19.8) 288 (21.5) 447 (33.8) 0.000
 2nd quartile 264 (19.7) 357 (26.7) 379 (28.6)
 3rd quartile 370 (27.7) 340 (25.4) 290 (21.9)
 4th quartile 439 (32.8) 354 (26.4) 207 (15.6)
WHR
 1st quartile 292 (21.8) 351 (26.2) 354 (26.8) 0.000
 2nd quartile 282 (21.1) 323 (24.1) 357 (27.0)
 3rd quartile 339 (25.3) 331 (24.7) 370 (28.0)
 4th quartile 425 (31.8) 334 (24.9) 241 (18.2)
RTF
 1st quartile 384 (28.7) 343 (25.6) 273 (20.6) 0.000
 2nd quartile 348 (26.0) 334 (24.9) 319 (24.1)
 3rd quartile 326 (24.4) 316 (23.6) 357 (27.0)
 4th quartile 280 (20.9) 346 (25.8) 374 (28.3)

BMI quartiles: 1st, < 21.57; 2nd, 21.57– < 23.53; 3rd, 23.53− < 25.72; 4th, ≥ 25.72. BFI quartiles: 1st, < 5.41; 2nd, 5.41– < 6.88; 3rd, 6.88– < 8.59; 4th, ≥ 8.59. FLMR quartiles: 1st, < 0.34; 2nd, 0.34– < 0.43; 3rd, 0.43– < 0.56; 4th, ≥ 0.56. WHR quartiles: 1st, < 0.88; 2nd, 0.88– < 0.92; 3rd, 0.92– < 0.97; 4th, ≥ 0.97. RTF quartiles: 1st, < 0.50; 2nd, 0.50– < 0.54; 3rd, 0.54– < 0.58; 4th, ≥ 0.58

P values were obtained by using chi-square test

BFI body fat index, BMI body mass index, FLMR fat–lean mass ratio, RTF relative truncal fat, WHR waist to hip ratio

aFitness was assessed with a 6-m walk test. Fitness tertiles: 1st, walking speed < 0.88 m/s (low fitness); 2nd, walking speed 0.88– < 1.05 m/s (moderate fitness); 3rd, walking speed ≥ 1.05 m/s (high fitness)

In general, within each quartile of fatness indicator, there was a significant trend towards reduced mortality with increasing fitness. For BMI and FLMR, this trend was not observed for the highest quartile, suggesting that fitness does not have any beneficial effect on health outcome in terms of mortality for those in the highest quartiles of total body fat indicators (BMI, FLMR) (Tables 5 and 6). However, the protective effect of fitness was observed for all quartiles of abdominal obesity indicators (WHR and RTF) including the highest quartile (Tables 7 and 8).

Table 5.

Multivariate proportional mortality hazard ratios (HRs) by body mass index (BMI) and fitness category in study participants

Fitness categorya No. of subjects No. (%) of deaths P trendb HR (95% CI)c P value
BMI < 18.5 (kg/m2)
 Low fitness 84 29 (34.5) 0.018 3.34 (2.13–5.24) 0.000
 Moderate fitness 63 15 (23.8) 2.67 (1.54–4.73) 0.001
 High fitness 68 12 (17.6) 2.17 (1.18–4.01) 0.013
BMI 18.5–24.9 (kg/m2)
 Low fitness 763 115 (15.1) 0.000 1.61 (1.19–2.18) 0.002
 Moderate fitness 823 102 (12.4) 1.54 (1.14–2.07) 0.005
 High fitness 885 76 (8.6) 1 (reference)
BMI 25.0–29.9 (kg/m2)
 Low fitness 436 59 (13.5) 0.010 1.66 (1.17–2.36) 0.005
 Moderate fitness 414 40 (9.7) 1.22 (0.83–1.80) 0.315
 High fitness 340 27 (7.9) 0.92 (0.59–1.43) 0.697
BMI ≥ 30.0 (kg/m2)
 Low fitness 55 6 (10.9) 0.874 1.65 (0.71–3.84) 0.242
 Moderate fitness 39 2 (5.1) 0.78 (0.19–3.19) 0.730
 High fitness 30 4 (13.3) 1.53 (0.56–4.22) 0.407

BMI body mass index, CI confidence interval

aFitness was assessed with a 6-m walk test. Fitness tertiles: 1st, walking speed < 0.88 m/s (low fitness); 2nd, walking speed 0.88– < 1.05 m/s (moderate fitness); 3 rd, walking speed ≥ 1.05 m/s (high fitness)

b P values for trend were obtained by using chi-square test (linear-by-linear association)

cAdjusted for age, sex, medical history (diabetes, stroke, hypertension, myocardial infarction, angina, and congestive heart failure), current smoking, and CVD medications (ACE inhibitor, aspirin, beta blocker, calcium channel blocker, and statin)

Table 6.

Multivariate proportional mortality hazard ratios (HRs) by fat–lean mass ratio (FLMR) and fitness category in study participants

Fitness categorya No. of subjects No. (%) of deaths P trendsb HR (95% CI)c P value
FLMR 1st quartile
 Low fitness 265 74 (27.9) 0.000 2.16 (1.07–4.39) 0.033
 Moderate fitness 288 69 (24.0) 2.31 (1.13–4.70) 0.022
 High fitness 447 53 (11.9) 1.15 (0.56–2.36) 0.715
FLMR 2nd quartile
 Low fitness 264 54 (20.5) 0.000 1.59 (0.78–3.24) 0.205
 Moderate fitness 357 48 (13.4) 1.30 (0.63–2.67) 0.480
 High fitness 379 37 (9.8) 1.00 (0.48–2.09) 0.993
FLMR 3rd quartile
 Low fitness 370 46 (12.4) 0.007 1.44 (0.72–2.89) 0.303
 Moderate fitness 340 26 (7.6) 1.02 (0.49–2.13) 0.964
 High fitness 290 19 (6.6) 0.97 (0.45–2.11) 0.934
FLMR 4th quartile
 Low fitness 439 35 (8.0) 0.063 1.24 (0.61–2.51) 0.555
 Moderate fitness 354 16 (4.5) 0.89 (0.40–1.96) 0.764
 High fitness 207 10 (4.8) 1 (reference)

FLMR quartiles: 1st, < 0.34; 2nd, 0.34– < 0.43; 3rd, 0.43– < 0.56; 4th, ≥ 0.56

CI confidence interval, FLMR fat–lean mass ratio

aFitness was assessed with a 6-m walk test. Fitness tertiles: 1st, walking speed < 0.88 m/s (low fitness); 2nd, walking speed 0.88– < 1.05 m/s (moderate fitness); 3 rd, walking speed ≥ 1.05 m/s (high fitness)

b P values for trend were obtained by using chi-square test (linear-by-linear association)

cAdjusted for age, sex, medical history (diabetes, stroke, hypertension, myocardial infarction, angina, and congestive heart failure), current smoking, and CVD medications (ACE inhibitor, aspirin, beta blocker, calcium channel blocker, and statin)

Table 7.

Multivariate proportional mortality hazard ratios (HRs) by waist–hip ratio (WHR) and fitness category in study participants

Fitness categorya No. of subjects No. (%) of deaths P trendsb HR (95% CI)c P value
WHR 1st quartile
 Low fitness 292 52 (17.8) 0.001 2.68 (1.62–4.42) 0.000
 Moderate fitness 351 39 (11.1) 2.06 (1.23–3.46) 0.006
 High fitness 354 33 (9.3) 1.65 (0.97–2.81) 0.067
WHR 2nd quartile
 Low fitness 282 26 (9.2) 0.177 1.39 (0.79–2.45) 0.260
 Moderate fitness 323 37 (11.5) 1.88 (1.12–3.18) 0.017
 High fitness 357 23 (6.4) 1 (reference)
WHR 3rd quartile
 Low fitness 339 56 (16.5) 0.026 2.42 (1.47–3.96) 0.000
 Moderate fitness 331 43 (13.0) 2.04 (1.23–3.39) 0.006
 High fitness 370 40 (10.8) 1.60 (0.96–2.67) 0.074
WHR 4th quartile
 Low fitness 425 75 (17.6) 0.002 2.58 (1.60–4.18) 0.000
 Moderate fitness 334 40 (12.0) 1.89 (1.13–3.17) 0.016
 High fitness 241 23 (9.5) 1.31 (0.73–2.34) 0.366

WHR quartiles: 1st, < 0.88; 2nd, 0.88– < 0.92; 3rd, 0.92– < 0.97; 4th, ≥ 0.97

CI confidence interval, WHR waist to hip ratio

aFitness was assessed with a 6-m walk test. Fitness tertiles: 1st, walking speed < 0.88 m/s (low fitness); 2nd, walking speed 0.88– < 1.05 m/s (moderate fitness); 3rd, walking speed ≥ 1.05 m/s (high fitness)

b P values for trend were obtained by using chi-square test (linear-by-linear association)

cAdjusted for age, sex, medical history (diabetes, stroke, hypertension, myocardial infarction, angina, and congestive heart failure), current smoking, and CVD medications (ACE inhibitor, aspirin, beta blocker, calcium channel blocker, and statin)

Table 8.

Multivariate proportional mortality hazard ratios (HRs) by relative truncal fat (RTF) and fitness category in study participants

Fitness categorya No. of subjects No. (%) of deaths P trendsb HR (95% CI)c P value
RTF 1st quartile
 Low fitness 384 60 (15.6) 0.033 2.32 (1.40–3.83) 0.001
 Moderate fitness 343 38 (11.1) 1.91 (1.13–3.24) 0.017
 High fitness 273 28 (10.3) 1.70 (0.97–2.98) 0.063
RTF 2nd quartile
 Low fitness 348 48 (13.8) 0.004 1.93 (1.15–3.23) 0.012
 Moderate fitness 334 36 (10.8) 1.73 (1.02–2.95) 0.043
 High fitness 319 22 (6.9) 1 (Reference)
RTF 3rd quartile
 Low fitness 326 54 (16.6) 0.003 1.73 (1.05–2.87) 0.033
 Moderate fitness 316 39 (12.3) 1.58 (0.94–2.67) 0.087
 High fitness 357 32 (9.0) 1.06 (0.61–1.83) 0.837
RTF 4th quartile
 Low fitness 280 47 (16.8) 0.009 1.50 (0.90–2.52) 0.123
 Moderate fitness 346 46 (13.3) 1.27 (0.76–2.12) 0.365
 High fitness 374 37 (9.9) 0.93 (0.55–1.58) 0.789

RTF quartiles: 1st, < 0.50; 2nd, 0.50– < 0.54; 3rd, 0.54– < 0.58; 4th, ≥ 0.58

CI confidence interval, RTF relative truncal fat

aFitness was assessed with a 6-m walk test. Fitness tertiles: 1st, walking speed < 0.88 m/s (low fitness); 2nd, walking speed 0.88– < 1.05 m/s (moderate fitness); 3 rd, walking speed ≥ 1.05 m/s (high fitness)

b P values for trend were obtained by using chi-square test (linear-by-linear association)

cAdjusted for age, sex, medical history (diabetes, stroke, hypertension, myocardial infarction, angina, and congestive heart failure), current smoking, and CVD medications (ACE inhibitor, aspirin, beta blocker, calcium channel blocker, and statin)

Discussion

This study showed that among an elderly population with a mean age of 72 years, higher measures of body fat, particularly FLMR and RTF, were associated with lower mortality, confirming results of previous studies using BMI, and the observation of an obesity paradox. It also confirms that lower cardiorespiratory fitness as measured by the 6-m walk was associated with increased mortality. However, no interaction between fatness and fitness measures was detected with respect to mortality, although within each fatness quartile for measures of abdominal fat (RTF and WHR) and for total body fat (BMI and FLMR) except for the highest quartile, increasing levels of fitness was associated with decreasing mortality. Fitness did not account for the obesity paradox, since higher levels of fitness were not present in subjects with higher BMI or other fatness measures, with the exception of RTF. The finding of higher level of fitness in those with higher RTF in Table 4 is difficult to explain, as it is against the trend for other fatness indicators. It is unlikely to be explained by a different association between fitness and abdominal fatness compared with total body fatness, since this was not observed for another measure of abdominal fatness, the waist to hip ratio (WHR). The finding may be related to the method of analysis, since Table 4 represents a cross-sectional association between fatness and fitness, and the results may be misleading compared with prospective analyses using Cox proportional hazards model. Using the latter method, both measures of abdominal fat (WHR and RTF) gave the same trends, with lower hazard ratios for mortality with increasing fatness quartiles and a decreasing mortality trend with increasing fitness within each fatness quartile.

This finding contrasts with other studies of the general adult population (Fogelholm 2010) and does not support the suggestion that fitness may account for the obesity paradox as suggested by McAuley et al. (2010a). Two previous prospective studies were carried out in elderly Caucasian cohorts. Sui et al. (2007) followed up 2087 men and 516 women aged 60–100 years in the USA for a mean of 12 years and showed that for all BMI categories 18–≥ 35 kg/m2, mortality risk was highest among these classified as unfit compared with those who were fit. In another study of 981 men with a mean age of 65 years, mortality was increased for those with BMI < 20 kg/m2 and decreased with increasing BMI values to ≥ 35 kg/m2, being lowest in the latter group. Mortality risk also decreased with increasing fitness (McAuley et al. 2009). The lowest mortality risk occurred among the obese, highly fit participants. It is interesting to speculate on the underlying mechanism(s) for the obesity paradox, if cardiorespiratory fitness is unlikely to be a factor. It is possible that among older people aged 70 years and over, weight loss exerts a greater impact on mortality as it may be an indicator of frailty (Morley 2007) and that higher levels of body fat may represent better reserve for episodes of acute illness when negative energy balance is more likely to occur.

This study also provides another novel contribution to existing literature, in that we were able to examine fatness indicators other than BMI, and such analyses have not been carried out previously. It is recognized that BMI may have limitations as the main marker for obesity. Total body fat, fat to lean mass ratio, and the distribution of body fat may be better indicators. The findings of this study also have important implications for public health, in highlighting that promotion/maintenance of fitness reduces mortality even in old age, whatever the level of body fatness. Furthermore, those with the lowest quartile of fatness measures have the highest mortality, irrespective of fitness levels. These findings show that public health guidelines for the general adult population may need to be modified for people aged 70 years and above, placing the emphasis on avoiding of weight loss as well as maintenance of fitness, rather than on weight reduction towards values for middle-age adults. These observations are important in view of the growing numbers of people in this age group, with population ageing in many developed countries.

Another novel aspect of this study is the assessment of walking speed as an indicator of cardiorespiratory fitness. This has not been examined in younger adult population, who may undertake treadmill or bicycle test with the measurement of maximal oxygen uptake with little difficulty. However, ageing adults may have increasing difficulty with using this equipment as a result of various stages of functional decline, so alternative safer and less costly assessments based on self-walking test have been developed. These are based on the distance covered by the subject within a defined time. Originally a 12-min walk test was developed to predict maximal oxygen uptake among athletes (Cooper 1968), and later a 6-min walk test became widely used for assessing older people with a wide spectrum of health and functional state (Simonsick et al. 2000; Troosters et al. 1999). We further adapted this measure to use the time taken to walk along a corridor over a distance of 6 m, recognizing that fitness may be underestimated as the warm-up effect may be lost due to the short distance walked. The advantage is that it is quick and suitable for the clinical and epidemiological research settings where associations with health outcomes and monitoring changes with time may be more important than accurate absolute values. The use of walking speed as an indicator of fitness is more accurate than assessment of physical activity using questionnaire such as the Physical Activity Scale for the Elderly (PASE) (Washburn et al. 1993). In a subgroup of 754 men and 488 women in whom maximal oxygen uptake was measured during the follow-up period, the age-adjusted correlation between maximal oxygen uptake with PASE was only 0.24 in men and 0.21 in women (Yau 2011). Recently, slow walking speed was shown to be a predictor of cardiovascular death in a French cohort study (Dumurgier et al. 2009).

Walking speed as a measure of fitness is particularly relevant for older populations with respect to gradual decline into the frail state, a physiological syndrome characterized by decreased reserve and diminished resistance to stressors as a result of cumulative decline across multiple physiological systems. Slow walking speed has been included as one of the features of the frailty phenotype (Fried et al. 2001) and indicator of frailty (Harwood and Conroy 2009), as well as one of the definitions of sarcopenia (Cruz-Jentoft et al. 2010). For the latter a cut-off value of walking speed of 1 m/s had been proposed. In our study, the high fitness category had a walking speed of ≥ 1.05 m/s, a value associated with lowest mortality and also ameliorating the adverse impact of body fatness on health outcomes.

There are limitations in this study. The participants were not representative of the Hong Kong population, in that their education level was higher. The results may not be strictly comparable with other studies that used different measures of cardiorespiratory fitness. Nevertheless, we have attempted to validate the use of walking speed in a subsequent subgroup study where maximal oxygen uptake was measured. The numbers of participants in the lowest and highest categories of BMI were smaller compared with those in the 18.5–29.9 kg/m2 range. It is possible that the findings may be different with larger numbers. We chose these BMI categories for comparison with other studies examining cardiorespiratory fitness with health outcomes. For other fatness indicators, there were larger numbers in each subgroup as quartile values were used. The strengths of this study include the large number of participants, the inclusion of women, the relatively long duration of follow-up, the use of DEXA to measure body composition, and adjustment for multiple potential confounders.

In conclusion, the study confirms the beneficial effects of cardiorespiratory fitness on mortality but does not explain the obesity paradox. The findings underscore the importance of maintaining physical fitness through exercise and re-confirm the importance of weight maintenance in reducing mortality risk.

Acknowledgements

This study is supported by the SH Ho Centre for Gerontology and Geriatrics, the Centre for Nutritional Studies, Faculty of Medicine, The Chinese University of Hong Kong, and the Hong Kong Jockey Club Charities Trust.

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