Alanine Aminotransferase and Body Composition in Obese Men and Women.
Svein Ivar BekkelundRolf JordePublished in: Disease markers (2019)
There is a known relationship between serum alanine aminotransferase (ALT) and obesity in humans, but the mechanism(s) are not clarified. This study investigated the associations between serum ALT and body composition in an overweight and obese population. The results are based on data from a previous randomized controlled trial treating obesity with vitamin D3. A sample of 448 overweight and obese individuals underwent dual-energy X-ray absorptiometry (DEXA) and measured serum ALT along with supplementary blood samples at study baseline. Body fat mass and lean mass indexes were calculated by dividing total body fat/lean weight (kg) by body height squared (kg/m2). ALT correlated with body mass index (BMI) in men but not women (r = 0.33, P < 0.0001 vs. r = 0.06, P = 0.29). In men, serum ALT correlated positively with fat mass index (r = 0.23, P = 0.004) and lean mass index (r = 0.32, P < 0.0001). In women, ALT correlated with lean mass index (r = 0.13, P = 0.031) but not fat mass index (r = 0.003, P = 0.96). In a multivariate model adjusted for age and fat mass index, a 1-unit increase in lean mass index associated with a 0.37 U/L higher ALT in the male subgroup (95% CI 0.024 to 0.040, P < 0.0001). In conclusion, serum ALT was associated with body fat mass index in men and with lean mass index in men and women in an overweight and obese population. The findings also demonstrate a gender difference in the role of fat.
Keyphrases
- body composition
- bone mineral density
- body mass index
- randomized controlled trial
- adipose tissue
- dual energy
- metabolic syndrome
- weight gain
- weight loss
- insulin resistance
- magnetic resonance imaging
- postmenopausal women
- resistance training
- physical activity
- study protocol
- machine learning
- bariatric surgery
- systematic review
- mental health
- mass spectrometry
- middle aged
- high fat diet induced
- data analysis
- breast cancer risk