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Splenomegaly is a Marker of Advanced Chronic Liver Disease and Portal Hypertension in HIV Infection

Overview
Journal HIV Med
Publisher Wiley
Date 2022 Aug 30
PMID 36042533
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Abstract

Objectives: To evaluate the clinical significance of splenomegaly as a marker of underlying liver disease in people with HIV (PWH).

Methods: We included consecutive PWH from a prospective cohort from 2010 to 2020 with available liver stiffness measurement (LSM) and liver imaging to define splenomegaly (> 13 cm) within 1 year. Cut-offs of LSM > 10 kPa and > 21 kPa were used to identify advanced chronic liver disease (ACLD) and portal hypertension, respectively. Logistic regression multivariable analysis was employed to identify independent predictors of ACLD.

Results: In all, 331 PWH were included, 76% of them men, with a median (interquartile range) age of 51.3 (45-58) years, all receiving antiretroviral treatment, and 53% were HIV monoinfected. The PWH with splenomegaly exhibited a higher prevalence of ACLD compared with those with normal spleen size, as per LSM (26% vs. 9%; p = 0.009). Portal hypertension diagnosed by LSM was also more prevalent in PWH with splenomegaly than in those without (15% vs. 2%; p < 0.001). Independent predictors of ACLD were viral hepatitis coinfection [adjusted odds ratio (aOR) = 3.15, 95% confidence interval (CI): 1.65-6.0], lower platelets (aOR = 0.99, 95% CI: 0.99-0.99) and splenomegaly (aOR = 2.41, 95% CI: 1.17-4.99). In patients with available oesophagogastroduodenoscopy, splenomegaly was also associated with higher prevalence of oesophageal varices and other endoscopic findings of portal hypertension (38% vs. 17%; p = 0.027).

Conclusions: Splenomegaly identified on routine imaging may have utility as a marker of ACLD and portal hypertension, prompting further investigations.

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Exploring the Correlation Between Splenomegaly and Lung Involvement in COVID-19: A Retrospective Study.

Raju B, Selvaraj B, Murugesan S, Balasubramaniam S, Pk S, Raviganesh P Cureus. 2024; 16(3):e55415.

PMID: 38567206 PMC: 10985569. DOI: 10.7759/cureus.55415.