Cleveland Clinic, Cleveland, Ohio, USA.
Department of Pathology, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Aliment Pharmacol Ther. 2024 Nov;60(10):1351-1360. doi: 10.1111/apt.18236. Epub 2024 Sep 5.
Metabolic dysfunction-associated steatotic liver disease (MASLD) is common in people with HIV (PWH). The morphological spectrum of MASLD compared to matched controls and of the correlation between the NAFLD activity score (NAS) and fibrosis stage in PWH remains unknown.
Overall, 107 liver biopsies from PWH with MASLD (MASLD-PWH) were matched to 107 biopsies from individuals with MASLD and without HIV (MASLD controls) on age at biopsy, race/ethnicity, sex, type 2 diabetes, body mass index (BMI) and alanine aminotransferase (ALT) level. Biopsies were scored using NAS.
Compared to MASLD-controls, MASLD-PWH had lower steatosis grade (OR: 0.65, 95% CI: (0.47-0.90), p = 0.01), lower lobular inflammation grade (OR: 0.55, 95% CI: (0.34-0.89), p = 0.02), less portal inflammation (OR: 0.42, 95% CI: (0.25-0.72), p = 0.002) and less ballooned hepatocytes (OR: 0.60, 95% CI: (0.41-0.88), p = 0.01). Thus, NAS was lower in MASLD-PWH (OR: 0.69, 95% CI: (0.56-0.85), p < 0.001) than in MASLD controls. There was a trend towards lower prevalence of steatohepatitis in MASLD-PWH (OR: 0.84, 95% CI: (0.68-1.03), p = 0.09). A multivariate analysis demonstrated that MASLD-PWH cases had significantly less steatosis (OR: 0.66, p = 0.03), portal inflammation (OR: 0.34, p = 0.001) and ballooned hepatocytes (OR: 0.55, p = 0.01), yet higher stage fibrosis (OR: 1.42, p = 0.03) compared to MASLD controls.
The NAS and histological drivers of fibrosis (e.g. inflammation and hepatocyte ballooning) are less pronounced in MASLD-PWH, and yet fibrosis stage was generally higher when compared to matched controls with MASLD without HIV. This suggests HIV-specific factors beyond hepatic necroinflammation may contribute to fibrosis progression in MASLD-PWH.
代谢功能障碍相关脂肪性肝病(MASLD)在 HIV 感染者(PWH)中很常见。与匹配的对照组相比,MASLD 的形态谱以及 PWH 中 NAFLD 活动评分(NAS)与纤维化分期之间的相关性尚不清楚。
总体而言,对 107 例 MASLD-PWH 患者(MASLD-PWH)和 107 例 MASLD 无 HIV 感染患者(MASLD 对照组)的肝活检进行了匹配,匹配因素包括活检时的年龄、种族/民族、性别、2 型糖尿病、体重指数(BMI)和丙氨酸氨基转移酶(ALT)水平。使用 NAS 对活检进行评分。
与 MASLD 对照组相比,MASLD-PWH 的脂肪变性程度评分较低(OR:0.65,95%CI:(0.47-0.90),p=0.01),肝小叶炎症程度评分较低(OR:0.55,95%CI:(0.34-0.89),p=0.02),门静脉炎症程度较轻(OR:0.42,95%CI:(0.25-0.72),p=0.002),气球样肝细胞较少(OR:0.60,95%CI:(0.41-0.88),p=0.01)。因此,MASLD-PWH 的 NAS 评分较低(OR:0.69,95%CI:(0.56-0.85),p<0.001),低于 MASLD 对照组。MASLD-PWH 患者的脂肪性肝炎患病率呈下降趋势(OR:0.84,95%CI:(0.68-1.03),p=0.09)。多变量分析表明,MASLD-PWH 患者的脂肪变性(OR:0.66,p=0.03)、门静脉炎症(OR:0.34,p=0.001)和气球样肝细胞(OR:0.55,p=0.01)程度明显较低,但纤维化分期(OR:1.42,p=0.03)明显较高。
与 MASLD 对照组相比,MASLD-PWH 的 NAS 和纤维化的组织学驱动因素(如炎症和肝细胞气球样变)不那么明显,但与无 HIV 的 MASLD 匹配对照组相比,纤维化分期通常更高。这表明,除了肝脏坏死性炎症之外,HIV 特异性因素可能会导致 MASLD-PWH 患者的纤维化进展。