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患有 MASLD 个体一级亲属发生主要不良肝脏结局的风险。

Risk of major adverse liver outcomes among first-degree relatives of individuals with MASLD.

机构信息

Department of Medicine, Huddinge, Karolinska Institutet, Stockholm, Sweden.

Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.

出版信息

Liver Int. 2024 May;44(5):1253-1264. doi: 10.1111/liv.15874. Epub 2024 Feb 22.

Abstract

BACKGROUND & AIMS: Previous studies have suggested an increased risk of major adverse liver outcomes (MALO) in relatives of patients with metabolic dysfunction-associated steatotic liver disease (MASLD). However, granular and longitudinal evidence is lacking on the future risk of MALO among family members of individuals with MASLD.

METHODS

We identified 3526 first-degree relatives (FDRs) and 11 079 general population comparators to 1328 patients with MASLD diagnosed between 1974 and 2021, with detailed clinical data, including liver histology in 71% of patients. MALO was defined through diagnostic coding for cirrhosis or its complications. Cox regression models were used to estimate adjusted hazard ratios (aHRs) for MALO among FDRs compared to general population comparators. Cumulative incidence accounting for competing risks was calculated.

RESULTS

During a median follow-up of 13.4 years, there were 65 (2%, 1.12/1000 person-years) and 225 (2%, 1.26/1000 person-years) MALO events in FDRs and general population comparators respectively. After adjusting for demographic factors and comorbidities, FDRs were at no increased risk of MALO (aHR = 0.99, 95% CI: 0.74-1.33). Increased relative rates of MALOs were, however, observed in some subgroups, including parents, although absolute risk estimates were low and comparable to the general population.

CONCLUSIONS

FDRs of patients with MASLD did not have a higher rate of incident MALO than the general population. Since the absolute risk of MALO in relatives of patients with MASLD was low, these results do not support systematic screening of MASLD-related fibrosis in relatives of patients with MASLD.

摘要

背景与目的

先前的研究表明,代谢功能障碍相关脂肪性肝病(MASLD)患者的亲属发生主要不良肝脏结局(MALO)的风险增加。然而,缺乏关于 MASLD 患者亲属未来发生 MALO 风险的具体和纵向证据。

方法

我们确定了 3526 名一级亲属(FDRs)和 11079 名一般人群对照与 1974 年至 2021 年间诊断的 1328 名 MASLD 患者相匹配,这些患者有详细的临床数据,包括 71%的患者的肝脏组织学。MALO 通过肝硬化或其并发症的诊断编码来定义。使用 Cox 回归模型估计 FDRs 与一般人群对照相比发生 MALO 的调整后危险比(aHR)。计算考虑竞争风险的累积发病率。

结果

在中位数为 13.4 年的随访期间,FDRs 和一般人群对照中分别有 65 例(2%,1.12/1000 人年)和 225 例(2%,1.26/1000 人年)发生 MALO 事件。在调整人口统计学因素和合并症后,FDRs 发生 MALO 的风险没有增加(aHR=0.99,95%CI:0.74-1.33)。然而,在一些亚组中观察到 MALO 的相对发生率增加,包括父母,但绝对风险估计较低,与一般人群相当。

结论

MASLD 患者的 FDRs 发生 MALO 的发生率不比一般人群高。由于 MASLD 患者亲属发生 MALO 的绝对风险较低,因此这些结果不支持对 MASLD 患者亲属进行 MASLD 相关纤维化的系统筛查。

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