TY - JOUR
T1 - Epicardial fat thickness correlates with body fat stores, insulin resistance and alanine aminotransferase in patients affected by nonalcoholic steatohepatitis (NASH)
AU - Capristo, Esmeralda
AU - Patti, Riccardo
AU - Malandrino, Noemi
AU - Farnetti, Sara
AU - Grieco, Antonio
AU - Mingrone, Geltrude
AU - Gasbarrini, Giovanni Battista
PY - 2010
Y1 - 2010
N2 - Introduction: Nonalcoholic steatohepatitis is frequently associated with obesity and metabolic
syndrome. The aim of the present study was to evaluate the relationship between epicardial fat
thickness, body composition, insulin resistance and alanine aminotransferase level in people affected
by nonalcoholic steatohepatitis.
Materials and methods: Fourteen adult male patients (body mass index [BMI] 28.8±2.0 kg/m2)
with biopsy-proven nonalcoholic steatohepatitis were enrolled in the study; 14 healthy men were
used as controls. All study participants underwent a clinical evaluation and an abdominal ultrasound
examination. A blood sample was drawn after an overnight fast for determination of plasma glucose,
insulin, HOMA-IR, blood lipids and parameters of liver and renal function. Epicardial fat thickness on
the free wall of the right ventricle from both parasternal long- and short-axis views and left ventricular
mass were measured by the same observer. Body composition was evaluated by anthropometry and
dual-energy absorptiometry.
Results: Epicardial fat thickness was greater in men with nonalcoholic steatohepatitis than in controls
(7.9±2.1 vs 4.1±1.8 mm, p<0.001) and correlated positively with percentage body fat (p<0.001), BMI
(p<0.001), waist circumference (p<0.001), HOMA-IR (p<0.01), and alanine aminotransferase level
(p<0.01).
Conclusion: The present study showed that epicardial fat thickness correlates with HOMA-IR and
body fat stores in subjects affected by nonalcoholic steatohepatitis. Since weight reduction is able
to reduce epicardial fat thickness in obese individuals, a correct dietary intervention program should
decrease epicardial fat thickness and insulin resistance, thus reducing cardiovascular risk factors in
patients with nonalcoholic steatohepatitis.
AB - Introduction: Nonalcoholic steatohepatitis is frequently associated with obesity and metabolic
syndrome. The aim of the present study was to evaluate the relationship between epicardial fat
thickness, body composition, insulin resistance and alanine aminotransferase level in people affected
by nonalcoholic steatohepatitis.
Materials and methods: Fourteen adult male patients (body mass index [BMI] 28.8±2.0 kg/m2)
with biopsy-proven nonalcoholic steatohepatitis were enrolled in the study; 14 healthy men were
used as controls. All study participants underwent a clinical evaluation and an abdominal ultrasound
examination. A blood sample was drawn after an overnight fast for determination of plasma glucose,
insulin, HOMA-IR, blood lipids and parameters of liver and renal function. Epicardial fat thickness on
the free wall of the right ventricle from both parasternal long- and short-axis views and left ventricular
mass were measured by the same observer. Body composition was evaluated by anthropometry and
dual-energy absorptiometry.
Results: Epicardial fat thickness was greater in men with nonalcoholic steatohepatitis than in controls
(7.9±2.1 vs 4.1±1.8 mm, p<0.001) and correlated positively with percentage body fat (p<0.001), BMI
(p<0.001), waist circumference (p<0.001), HOMA-IR (p<0.01), and alanine aminotransferase level
(p<0.01).
Conclusion: The present study showed that epicardial fat thickness correlates with HOMA-IR and
body fat stores in subjects affected by nonalcoholic steatohepatitis. Since weight reduction is able
to reduce epicardial fat thickness in obese individuals, a correct dietary intervention program should
decrease epicardial fat thickness and insulin resistance, thus reducing cardiovascular risk factors in
patients with nonalcoholic steatohepatitis.
KW - insulin resistance
KW - liver steatosis
KW - obesity
KW - insulin resistance
KW - liver steatosis
KW - obesity
UR - http://hdl.handle.net/10807/7932
M3 - Article
SN - 1828-6232
SP - 137
EP - 142
JO - NUTRITIONAL THERAPY & METABOLISM
JF - NUTRITIONAL THERAPY & METABOLISM
ER -