Center of Nutrition for the Research and the Care of Obesity and Metabolic Diseases, National Institute of Gastroenterology IRCCS "Saverio de Bellis", Castellana Grotte, 70013 Bari, Italy.
Laboratory of Epidemiology and Statistics, National Institute of Gastroenterology "Saverio de Bellis", IRCCS Hospital, Castellana Grotte, 70013 Bari, Italy.
Nutrients. 2024 May 8;16(10):1408. doi: 10.3390/nu16101408.
Obesity and metabolic syndrome are linked to steatotic liver disease (SLD), the most common form of chronic liver disease. Lifestyle modifications and dieting are strategies that can prevent metabolic dysfunction-associated steatotic liver disease (MASLD). The very low-calorie ketogenic diet (VLCKD) is a helpful treatment for MASLD and has been recommended for people affected by obesity; we evaluated the effect of gender on steatosis and fibrosis in a cohort of 112 overweight or obese patients undergoing an eight-week treatment with a VLCKD. Differences between the genders in terms of anthropometric measures, body composition, and metabolic indicators were examined before, during, and after the nutritional intervention. At baseline, there were significant differences between men and women in terms of anthropometric parameters, blood pressure, Homeostatic Model Assessment for Insulin Resistance (HOMA-IR), fasting insulin, hepatic markers, and lipid profile. Men had considerably higher levels of liver steatosis (measured by CAP) and liver stiffness (measured by E) under basal conditions than women. After the VLCKD, there were reductions in both genders of controlled attenuation parameter (CAP), body weight, body mass index (BMI), waist circumference, systolic and diastolic blood pressure, insulin resistance, fat mass (FM), free fat mass (FFM), and fasting blood glucose, insulin, glycated hemoglobin (HbA1c), triglycerides, total cholesterol, low-density lipoprotein (LDL) cholesterol, alanine transaminase (ALT), gamma-glutamyl transferase (γGT), and uric acid levels. Only in men, liver stiffness, aspartate aminotransferase (AST), creatinine, and C-reactive protein (CRP) levels significantly decreased. Moreover, men had significantly greater levels of liver steatosis: the male gender featured an increase of 23.96 points of the Fibroscan CAP. Men exhibited higher levels of steatosis and fibrosis than women, and these differences persist despite VLCKD. These gender-specific variations in steatosis and fibrosis levels could be caused by hormonal and metabolic factors, suggesting that different therapeutic strategies might be required depending on the gender.
肥胖和代谢综合征与脂肪性肝病(SLD)有关,这是最常见的慢性肝病形式。生活方式的改变和节食是预防代谢功能障碍相关脂肪性肝病(MASLD)的策略。极低卡路里生酮饮食(VLCKD)是治疗 MASLD 的有效方法,已被推荐用于肥胖人群;我们评估了性别对 112 名超重或肥胖患者接受 8 周 VLCKD 治疗后脂肪变性和纤维化的影响。在营养干预之前、期间和之后,检查了性别之间在人体测量学指标、身体成分和代谢指标方面的差异。在基线时,男性和女性在人体测量参数、血压、胰岛素抵抗稳态模型评估(HOMA-IR)、空腹胰岛素、肝标志物和血脂谱方面存在显著差异。在基础状态下,男性的肝脂肪变性(通过 CAP 测量)和肝硬度(通过 E 测量)明显高于女性。在 VLCKD 后,两种性别均降低了受控衰减参数(CAP)、体重、体重指数(BMI)、腰围、收缩压和舒张压、胰岛素抵抗、脂肪量(FM)、去脂体重(FFM)和空腹血糖、胰岛素、糖化血红蛋白(HbA1c)、甘油三酯、总胆固醇、低密度脂蛋白(LDL)胆固醇、丙氨酸转氨酶(ALT)、γ-谷氨酰转移酶(γGT)和尿酸水平。只有男性的肝硬度、天冬氨酸转氨酶(AST)、肌酐和 C 反应蛋白(CRP)水平显著降低。此外,男性的肝脂肪变性水平显著更高:男性 Fibroscan CAP 增加了 23.96 分。男性的脂肪变性和纤维化水平高于女性,尽管进行了 VLCKD,但这些差异仍然存在。脂肪变性和纤维化水平的这些性别特异性差异可能是由激素和代谢因素引起的,这表明可能需要根据性别采用不同的治疗策略。