TY - JOUR
T1 - Low- and high-density lipoprotein subclasses in subjects with nonalcoholic fatty liver disease
AU - Rizzo, Manfredi
AU - Nikolic, Dragana
AU - Montalto, Giuseppe
AU - Genc, Halil
AU - Banach, Maciej
AU - Cesur, Mustafa
AU - Ercin, Cemal Nuri
AU - Rizzo, Manfredi
AU - Karslioʇlu, Yildirim
AU - Dogru, Teoman
AU - Sonmez, Alper
AU - Bagci, Sait
AU - Toth, Peter P.
AU - Rizzo, Manfredi
AU - Tapan, Serkan
PY - 2015
Y1 - 2015
N2 - Background Nonalcoholic fatty liver disease (NAFLD) is associated with increased cardiometabolic risk. Although dyslipidemia represents a key factor in this disease, its impact on serum levels of distinct lipoprotein subfractions is largely unknown. Objective To assess the full low-density lipoprotein (LDL) and high-density lipoprotein (HDL) profiles in patients with NAFLD. Methods Seven LDL and 10 HDL subfractions were assessed by gel electrophoresis (Lipoprint, Quantimetrix Corporation, USA) in men with biopsy proven NAFLD (simple steatosis [n = 17, age, 34 ± 7 years] and nonalcoholic steatohepatitis [NASH; n = 24, age, 32 ± 6 years]). Exclusion criteria included robust alcohol consumption, infection with hepatitis B or C virus, body mass index ≥40 kg/m2, diabetes mellitus, and hypertension. Results Compared with simple steatosis, NASH patients had similar body mass index, homeostasis model assessment of insulin resistance index and plasma lipids, with increased levels of both aspartate aminotransferase and alanine transaminase. NASH subjects had lower levels of larger LDL1 (10 ± 4 vs 13 ± 4%, P =.010) and increased smaller LDL3 and LDL4 particles (9 ± 5 vs 5 ± 5%, P =.017 and 3 ± 3 vs 1 ± 2%, P =.012, respectively). No changes were found in the HDL subclass profile. By multiple regression analysis, we found that NASH was associated only with increased levels of LDL3 (P =.0470). Conclusions The increased levels of small, dense LDL3 and LDL4 in NASH may help to at least partly explain the increased risk for atherosclerosis and cardiovascular diseases in these patients.
AB - Background Nonalcoholic fatty liver disease (NAFLD) is associated with increased cardiometabolic risk. Although dyslipidemia represents a key factor in this disease, its impact on serum levels of distinct lipoprotein subfractions is largely unknown. Objective To assess the full low-density lipoprotein (LDL) and high-density lipoprotein (HDL) profiles in patients with NAFLD. Methods Seven LDL and 10 HDL subfractions were assessed by gel electrophoresis (Lipoprint, Quantimetrix Corporation, USA) in men with biopsy proven NAFLD (simple steatosis [n = 17, age, 34 ± 7 years] and nonalcoholic steatohepatitis [NASH; n = 24, age, 32 ± 6 years]). Exclusion criteria included robust alcohol consumption, infection with hepatitis B or C virus, body mass index ≥40 kg/m2, diabetes mellitus, and hypertension. Results Compared with simple steatosis, NASH patients had similar body mass index, homeostasis model assessment of insulin resistance index and plasma lipids, with increased levels of both aspartate aminotransferase and alanine transaminase. NASH subjects had lower levels of larger LDL1 (10 ± 4 vs 13 ± 4%, P =.010) and increased smaller LDL3 and LDL4 particles (9 ± 5 vs 5 ± 5%, P =.017 and 3 ± 3 vs 1 ± 2%, P =.012, respectively). No changes were found in the HDL subclass profile. By multiple regression analysis, we found that NASH was associated only with increased levels of LDL3 (P =.0470). Conclusions The increased levels of small, dense LDL3 and LDL4 in NASH may help to at least partly explain the increased risk for atherosclerosis and cardiovascular diseases in these patients.
KW - Diabetes and Metabolism; Internal Medicine; Nutrition and Dietetics; Medicine (all)
KW - HDL; Lipoproteins
KW - LDL; Male; Middle Aged; Non-alcoholic Fatty Liver Disease; Risk Factors; Cardiology and Cardiovascular Medicine; Endocrinology
KW - Lipids; Lipoproteins; Nonalcoholic fatty liver disease; Nonalcoholic steatohepatitis; Simple steatosis; Adult; Alanine Transaminase; Aspartate Aminotransferases; Atherosclerosis; Body Mass Index; Fatty Liver; Female; Humans; Lipoproteins
KW - Diabetes and Metabolism; Internal Medicine; Nutrition and Dietetics; Medicine (all)
KW - HDL; Lipoproteins
KW - LDL; Male; Middle Aged; Non-alcoholic Fatty Liver Disease; Risk Factors; Cardiology and Cardiovascular Medicine; Endocrinology
KW - Lipids; Lipoproteins; Nonalcoholic fatty liver disease; Nonalcoholic steatohepatitis; Simple steatosis; Adult; Alanine Transaminase; Aspartate Aminotransferases; Atherosclerosis; Body Mass Index; Fatty Liver; Female; Humans; Lipoproteins
UR - http://hdl.handle.net/10447/197817
UR - http://www.elsevier.com/wps/find/journaldescription.cws_home/710566/description#description
M3 - Article
SN - 1933-2874
VL - 9
SP - 576
EP - 582
JO - Journal of Clinical Lipidology
JF - Journal of Clinical Lipidology
ER -