The value of different CT‐based methods for diagnosing low muscle mass and predicting mortality in patients with cirrhosis

Liver International - Tập 39 Số 12 - Trang 2374-2385 - 2019
Rafael Paternostro1,2, Katharina Lampichler3, Constanze Bardach3, Ulrika Asenbaum3, Clara Landler1,2, David Bauer1,2, Mattias Mandorfer1,2, Rémy Schwarzer2, Michael Trauner1,2, Thomas Reiberger1,2, Arnulf Ferlitsch4,2
1Divison of Gastroenterology and Hepatology, Department of Internal Medicine III, Medical University of Vienna, Vienna, Austria
2Vienna Hepatic Hemodynamic Lab, Medical University of Vienna, Vienna, Austria
3Department of Biomedical Imaging and Image-guided Therapy, Medical University of Vienna, Vienna, Austria
4Department of Medicine I, Hospital St. John of God, Vienna, Austria

Tóm tắt

AbstractBackground & AimsLow muscle mass impacts on morbidity and mortality in cirrhosis. The skeletal‐muscle index (SMI) is a well‐validated tool to diagnose muscle wasting, but requires specialized radiologic software and expertise. Thus, we compared different Computed tomography (CT)‐based evaluation methods for muscle wasting and their prognostic value in cirrhosis.MethodsConsecutive cirrhotic patients included in a prospective registry undergoing abdominal CT scans were analysed. SMI, transversal psoas muscle thickness (TPMT), total psoas volume (TPV) and paraspinal muscle index (PSMI) were measured. Sarcopenia was defined using SMI as a reference method by applying sex‐specific cut‐offs (males: <52.4 cm2/m2; females: <38.5 cm2/m2).ResultsOne hundred and nine patients (71.6% male) of age 57 ± 11 years, MELD 16 (8‐26) and alcoholic liver disease (63.3%) as the main aetiology were included. According to established SMI cut‐offs, low muscle mass was present in 69 patients (63.3%) who also presented with higher MELD (17 vs 14 points; P = .025). The following optimal sex‐specific cut‐offs (men/women) for diagnosing low muscle mass were determined: TPMT: <10.7/ <7.8 mm/m, TPV: <194.9/ <99.2 cm3 and PSMI <26.3/ <20.8 cm2/m2. Thirty (27.5%) patients died during a follow‐up of 15 (0.3‐45.7) months. Univariate competing risks analyses showed a significant risk for mortality according to SMI (aSHR:2.52, 95% CI: 1.03‐6.21, P = .043), TPMT (aSHR: 3.87, 95% CI: 1.4‐8.09, P = .007) and PSMI (aSHR: 2.7, 95% CI: 1.17‐6.23, P = .02), but not TPV (P = .18) derived low muscle mass cut‐offs. In multivariate analysis only TPMT (aSHR: 2.82, 95% CI: 1.20‐6.67, P = .018) was associated with mortality, SMI (aSHR: 1.93, 95% CI: 0.72‐5.16, P = .19) and PSMI (aSHR: 1.93, 95% CI: 0.79‐4.75, P = .15) were not.ConclusionLow muscle mass was highly prevalent in our cohort of patients with cirrhosis. Gender‐specific TPMT, SMI and PSMI cut‐offs for low muscle mass can help identify patients with an increased risk for mortality. Importantly, only TPMT emerged as an independent risk factor for mortality in patients with cirrhosis.

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