TY - JOUR
T1 - Alcohol consumption and body composition in a population-based sample of elderly Australian men
AU - Coulson, Carolyn
AU - Williams, Lana
AU - Brennan, Sharon Lee
AU - Berk, Michael
AU - Kotowicz, Mark
AU - Lubman, Dan
AU - Pasco, Julie Anne
PY - 2013
Y1 - 2013
N2 - Alcohol is calorie dense, and impacts activity, appetite and lipid processing. The aim of this study was to therefore investigate the association between alcohol consumption and components of body composition including bone, fat and lean tissue. Methods: Participants were recruited from a randomly selected, population-based sample of 534 men aged 65 years and older enrolled in the Geelong Osteoporosis Study. Alcohol intake was ascertained using a food frequency questionnaire and the sample categorised as non-drinkers or alcohol users who consumed =2, 3-4 or =5 standard drinks on a usual drinking day. Bone mineral density (BMD), lean body mass and body fat mass were measured using dual energy X-ray absorptiometry; overall adiposity ( body fat), central adiposity ( truncal fat) and body mass index (BMI) were calculated. Bone quality was determined by quantitative heel ultrasound (QUS). Results: There were 90 current non-drinkers (16.9 ), 266 (49.8 ) consumed 1-2 drinks/day, 104 (19.5 ) 3-4 drinks/day and 74 (13.8 ) =5 drinks/day. Those consuming =5 drinks/day had greater BMI (+4.8 ), fat mass index (+20.1 ), waist circumference (+5.0 ), body fat (+15.2 ) and proportion of trunk fat (+5.3 ) and lower lean mass (-5.0 ) than non-drinkers after adjustment for demographic and lifestyle factors. Furthermore, they were more likely to be obese than non-drinkers according to criteria based on BMI (OR = 2.83, 95 CI 1.10-7.29) or waist circumference (OR = 3.36, 95 CI 1.32-8.54). There was an inverse relationship between alcohol consumption and QUS parameters and BMD at the mid forearm site; no differences were detected for BMD at other skeletal sites. Conclusion: Higher alcohol intake was associated with greater total and central adiposity and reduced bone quality
AB - Alcohol is calorie dense, and impacts activity, appetite and lipid processing. The aim of this study was to therefore investigate the association between alcohol consumption and components of body composition including bone, fat and lean tissue. Methods: Participants were recruited from a randomly selected, population-based sample of 534 men aged 65 years and older enrolled in the Geelong Osteoporosis Study. Alcohol intake was ascertained using a food frequency questionnaire and the sample categorised as non-drinkers or alcohol users who consumed =2, 3-4 or =5 standard drinks on a usual drinking day. Bone mineral density (BMD), lean body mass and body fat mass were measured using dual energy X-ray absorptiometry; overall adiposity ( body fat), central adiposity ( truncal fat) and body mass index (BMI) were calculated. Bone quality was determined by quantitative heel ultrasound (QUS). Results: There were 90 current non-drinkers (16.9 ), 266 (49.8 ) consumed 1-2 drinks/day, 104 (19.5 ) 3-4 drinks/day and 74 (13.8 ) =5 drinks/day. Those consuming =5 drinks/day had greater BMI (+4.8 ), fat mass index (+20.1 ), waist circumference (+5.0 ), body fat (+15.2 ) and proportion of trunk fat (+5.3 ) and lower lean mass (-5.0 ) than non-drinkers after adjustment for demographic and lifestyle factors. Furthermore, they were more likely to be obese than non-drinkers according to criteria based on BMI (OR = 2.83, 95 CI 1.10-7.29) or waist circumference (OR = 3.36, 95 CI 1.32-8.54). There was an inverse relationship between alcohol consumption and QUS parameters and BMD at the mid forearm site; no differences were detected for BMD at other skeletal sites. Conclusion: Higher alcohol intake was associated with greater total and central adiposity and reduced bone quality
UR - http://download.springer.com/static/pdf/827/art%253A10.1007%252Fs40520-013-0026-9.pdf?auth66=1399082665_372e29b46f70be720835aee3d9a33382&ext=.pdf
U2 - 10.1007/s40520-013-0026-9
DO - 10.1007/s40520-013-0026-9
M3 - Article
SN - 1594-0667
VL - 25
SP - 183
EP - 192
JO - Aging Clinical and Experimental Research
JF - Aging Clinical and Experimental Research
IS - 2
ER -