Elhoseeny Mohamed Mahmoud, Rageh Fatma, Bakry Nadia, Elgamal Rasha, Ahmed Samar S, Rezk Samar M, Othman Amira A A
Internal Medicine Department, Faculty of Medicine, Suez University, Suez, Egypt.
Infectious Diseases, Gastroenterology and Hepatology Department, Faculty of Medicine, Suez University, Suez, Egypt.
Lipids Health Dis. 2025 Sep 23;24(1):286. doi: 10.1186/s12944-025-02710-7.
Metabolic dysfunction-associated steatotic liver disease (MASLD) represents a growing public health challenge in Egypt, driven by westernized dietary patterns, urbanization, and physical inactivity. Despite lifestyle intervention being the first-line management, data on structured hypocaloric diets tailored to Egyptian patients remain limited, particularly regarding their effects on hepatic steatosis, inflammatory pathways, and oxidative stress biomarkers. This study aimed to evaluate the impact of a culturally adapted 6-month hypocaloric diet on hepatic fat reduction, metabolic parameters, inflammatory-oxidative biomarkers, and lifestyle factors in Egyptian MASLD patients, with additional exploration of weight-independent mechanisms.
In this single-center interventional trial, 30 newly diagnosed MASLD patients received a personalized hypocaloric diet (500-1000 kcal/day deficit). Outcomes measured at baseline and post-intervention included anthropometrics, liver enzymes, metabolic profile, hepatic steatosis (CAP score), inflammatory markers (TNF-α, MDA), antioxidant enzymes (SOD, CAT), and lifestyle behaviors (physical activity, sleep). Advanced statistical analyses included effect size estimation, multivariate regression, mediation analysis, and subgroup comparisons (lean vs. obese MASLD).
After 6 months, patients achieved significant reductions in weight (- 10.9 kg), BMI (- 3.9 kg/m), and CAP score (- 89.5 dB/m) (all P < 0.001). Liver enzymes improved significantly, with ALT decreasing by - 22.2 U/L and AST by - 21.3 U/L (both P < 0.001). TNF-α (- 88.2 pg/mL, baseline 166.1 pg/mL) and MDA (- 1.1 nmol/mL, baseline 2.7 nmol/mL) decreased markedly, with large effect sizes (CAP: d = 1.9; TNF-α: d = 2.1; MDA: d = 1.4). Antioxidant biomarkers improved significantly, with SOD increasing by 209% (d = 1.8) and CAT by 48.5% (d = 1.2) (both P < 0.001). Although BMI and weight loss were strongly associated with hepatic fat reduction, TNF-α reduction remained an independent predictor of CAP improvement (β = 0.31, P = 0.02), mediating 32% of the diet's effect after adjusting for BMI. Patients achieving ≥ 5% weight loss were 4.2 times more likely to experience ≥ 10% CAP score reduction. Lean MASLD patients (n = 6) exhibited greater improvements in hepatic fat and inflammation despite less weight loss; however, these findings should be interpreted with caution due to the small subgroup size. Dietary adherence strongly correlated with CAP reduction (r = - 0.71, P < 0.001) and antioxidant gains.
A culturally tailored hypocaloric diet effectively improved hepatic steatosis, inflammatory status, and antioxidant capacity in Egyptian MASLD patients. These improvements were partially weight-independent and partially mediated by anti-inflammatory responses. These findings support hypocaloric dietary strategies as a potentially scalable therapeutic option for MASLD management in resource-limited settings, though the absence of a control group limits causal inference, and further evaluation of implementation feasibility and cost-effectiveness is warranted. Additional benefits were also observed in lifestyle behaviors such as physical activity and sleep.
代谢功能障碍相关脂肪性肝病(MASLD)在埃及对公共卫生构成日益严峻的挑战,这是由西方化饮食模式、城市化和身体活动不足所驱动的。尽管生活方式干预是一线治疗方法,但针对埃及患者的结构化低热量饮食的数据仍然有限,尤其是关于其对肝脏脂肪变性、炎症途径和氧化应激生物标志物的影响。本研究旨在评估一种根据文化调整的为期6个月的低热量饮食对埃及MASLD患者肝脏脂肪减少、代谢参数、炎症 - 氧化生物标志物和生活方式因素的影响,并进一步探索与体重无关的机制。
在这项单中心干预试验中,30名新诊断的MASLD患者接受了个性化低热量饮食(每天热量 deficit 500 - 1000千卡)。在基线和干预后测量的结果包括人体测量学指标、肝酶、代谢谱、肝脏脂肪变性(CAP评分)、炎症标志物(TNF-α、MDA)、抗氧化酶(SOD、CAT)和生活方式行为(身体活动、睡眠)。先进的统计分析包括效应大小估计、多元回归、中介分析和亚组比较(瘦型与肥胖型MASLD)。
6个月后,患者的体重(-10.9千克)、BMI(-3.9千克/平方米)和CAP评分(-89.5分贝/米)均显著降低(所有P < 0.001)。肝酶显著改善,ALT降低了-22.2 U/L,AST降低了-21.3 U/L(两者P < 0.001)。TNF-α(-88.2皮克/毫升,基线为166.1皮克/毫升)和MDA(-1.1纳摩尔/毫升,基线为2.7纳摩尔/毫升)显著降低,效应大小较大(CAP:d = 1.9;TNF-α:d = 2.1;MDA:d = 1.4)。抗氧化生物标志物显著改善,SOD增加了209%(d = 1.8),CAT增加了48.5%(d = 1.2)(两者P < 0.001)。虽然BMI和体重减轻与肝脏脂肪减少密切相关,但TNF-α的降低仍然是CAP改善的独立预测因素(β = 0.31,P = 0.02),在调整BMI后介导了饮食效果的32%。体重减轻≥5%的患者CAP评分降低≥10%的可能性高出4.2倍。瘦型MASLD患者(n = 6)尽管体重减轻较少,但肝脏脂肪和炎症的改善更大;然而,由于亚组规模较小,这些发现应谨慎解释。饮食依从性与CAP降低(r = -0.71,P < 0.001)和抗氧化剂增加密切相关。
一种根据文化定制的低热量饮食有效地改善了埃及MASLD患者的肝脏脂肪变性、炎症状态和抗氧化能力。这些改善部分与体重无关,部分由抗炎反应介导。这些发现支持低热量饮食策略作为资源有限环境中MASLD管理的一种潜在可扩展的治疗选择,尽管缺乏对照组限制了因果推断,并且有必要进一步评估实施可行性和成本效益。在身体活动和睡眠等生活方式行为方面也观察到了额外的益处。