<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10(1)</volume><submitter>Sharma M</submitter><pubmed_abstract>A significant proportion of patients with non-alcoholic fatty liver disease (NAFLD) in Asian sub-continent are non-overweight and may have different underlying risk factors, lifestyles and metabolic profiles. Seven hundred fifty patients of NAFLD with raised alanine-amino-transferase (ALT) were divided into non-overweight and obese group based on their body mass index (BMI). Detailed dietary and lifestyle history were obtained through questionnaires and a detailed assessment of metabolic profile and liver stiffness was done. Normal BMI (&lt;?23 kg/m2) was found in 6.6% patients, of which 69.5% had raised ALT. Though the intake of dietary fat and exercise pattern were not different amongst these groups, yet the amount of aerated drinks was higher in obese subjects (12?±?17 vs. 7?±?7.5 p?=?0.005). Serum low-density lipoprotein (111?±?25.6 vs. 127.7?±?32.7 p?=?0.04) and insulin resistance based on HOMA-IR?>?2 were significantly higher in obese group (4.1?±?0.36 vs. 2.0?±?0.15 p?=?0.001). Insulin resistance and dyslipidemia were prevalent in 12% and 25% non-overweight patients respectively. Metabolic syndrome was more common in obese subjects. In addition, magnetic resonance elastography showed higher mean liver fat in the obese group with similar hepatic fibrosis. Non-overweight patients with NAFLD had lower insulin resistance and prevalence of dyslipidaemia at similar dietary and exercise pattern.</pubmed_abstract><journal>Scientific reports</journal><pagination>15232</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7499301</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Difference in lifestyle and metabolic profile of non-alcoholic fatty liver disease with raised alanine amino-transferases between obese and non-overweight subjects.</pubmed_title><pmcid>PMC7499301</pmcid><pubmed_authors>Gupta R</pubmed_authors><pubmed_authors>Kulkarni A</pubmed_authors><pubmed_authors>Nori VB</pubmed_authors><pubmed_authors>Jagtap N</pubmed_authors><pubmed_authors>Reddy DN</pubmed_authors><pubmed_authors>Rao PN</pubmed_authors><pubmed_authors>Kumar P</pubmed_authors><pubmed_authors>Sharma M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Difference in lifestyle and metabolic profile of non-alcoholic fatty liver disease with raised alanine amino-transferases between obese and non-overweight subjects.</name><description>A significant proportion of patients with non-alcoholic fatty liver disease (NAFLD) in Asian sub-continent are non-overweight and may have different underlying risk factors, lifestyles and metabolic profiles. Seven hundred fifty patients of NAFLD with raised alanine-amino-transferase (ALT) were divided into non-overweight and obese group based on their body mass index (BMI). Detailed dietary and lifestyle history were obtained through questionnaires and a detailed assessment of metabolic profile and liver stiffness was done. Normal BMI (&lt;?23 kg/m2) was found in 6.6% patients, of which 69.5% had raised ALT. Though the intake of dietary fat and exercise pattern were not different amongst these groups, yet the amount of aerated drinks was higher in obese subjects (12?±?17 vs. 7?±?7.5 p?=?0.005). Serum low-density lipoprotein (111?±?25.6 vs. 127.7?±?32.7 p?=?0.04) and insulin resistance based on HOMA-IR?>?2 were significantly higher in obese group (4.1?±?0.36 vs. 2.0?±?0.15 p?=?0.001). Insulin resistance and dyslipidemia were prevalent in 12% and 25% non-overweight patients respectively. Metabolic syndrome was more common in obese subjects. In addition, magnetic resonance elastography showed higher mean liver fat in the obese group with similar hepatic fibrosis. Non-overweight patients with NAFLD had lower insulin resistance and prevalence of dyslipidaemia at similar dietary and exercise pattern.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Sep</publication><modification>2020-10-09T07:07:36Z</modification><creation>2020-09-28T07:02:42Z</creation></dates><accession>S-EPMC7499301</accession><cross_references><pubmed>32943747</pubmed><doi>10.1038/s41598-020-72306-x</doi></cross_references></HashMap>