代谢功能障碍相关的脂肪变性肝病改变肝脏和脂肪组织中的脂肪酸谱。

Saana Palomurto, Kirsi A Virtanen, Vesa Kärjä, Ursula Schwab, Dorota Kaminska, Pirjo Käkelä, Jussi Pihlajamäki, Ville Männistö
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引用次数: 0

摘要

背景:代谢功能障碍相关脂肪变性肝病(MASLD)中全身脂肪酸(FA)代谢的改变尚不清楚。目的:研究MASLD患者FA代谢的组织间串音,我们比较了重度肥胖和正常肝脏、单纯性脂肪变性或代谢功能障碍相关脂肪性肝炎(MASH)患者的肝脏、血清、内脏和皮下脂肪组织中的FA谱。方法:对183例重度肥胖患者(女性122例,平均年龄46.9±9.7岁,体重指数43.5±5.7 kg/m2)进行腹腔镜胃分流术术前血清、肝脏、皮下及内脏脂肪组织采集。采用气液色谱法分析FA成分。采用Kruskal-Wallis试验比较不同组织库的FA比例。结果:脂肪肝患者肝脏FA比例变化大于脂肪组织FA比例。多不饱和脂肪酸(PUFA)在MASH患者肝脏中的比例明显低于正常肝脏(P < 0.01)。相反,二同γ -亚麻酸、肾上腺酸和花生四烯酸在MASH患者脂肪组织中的比例更高(调整后p < 0.001)。结论:MASH患者表现出肝脏PUFA含量降低,肝脏饱和FAs增加,n6 / n3 PUFA比值较高,而脂肪组织中没有明显的趋势。这些发现强调了脂肪肝和脂肪组织之间FA代谢的明显差异,强调了组织特异性调节机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Metabolic dysfunction-associated steatotic liver disease alters fatty acid profiles in the liver and adipose tissue.

Context: The alterations in systemic fatty acid (FA) metabolism in metabolic dysfunction-associated steatotic liver disease (MASLD) remain unclear.

Objective: To investigate inter-tissue crosstalk in FA metabolism in patients with MASLD, we compared FA profiles in the liver, serum, visceral, and subcutaneous adipose tissue of patients with severe obesity and normal liver, simple steatosis, or metabolic dysfunction-associated steatohepatitis (MASH).

Methods: Preoperative serum, liver, subcutaneous, and visceral adipose tissue samples were collected during laparoscopic gastric bypass surgery from 183 patients with severe obesity patients (122 women, mean age 46.9 ± 9.7 years, body mass index 43.5 ± 5.7 kg/m2). FA composition was analyzed using gas-liquid chromatography. The Kruskal-Wallis test was used to compare the FA proportions in different tissue depots.

Results: FA proportions varied more in the liver than in adipose tissue in patients with MASH. Polyunsaturated FAs (PUFA) proportions were significantly lower in the livers of patients with MASH than in those with normal livers (all adjusted P< 0.01). Conversely, dihomo-gamma-linolenic acid, adrenic acid, and arachidonic acid proportions were higher in the adipose tissues of patients with MASH (all adjusted p < 0.001).

Conclusions: Patients with MASH exhibited reduced hepatic PUFA content, increased hepatic saturated FAs, and a higher n6-to-n3 PUFA ratio, whereas no clear trends were observed in adipose tissue. These findings highlight distinct differences in FA metabolism between the liver and adipose tissue in MASLD, emphasizing tissue-specific regulatory mechanisms.

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