Comprehensive risk factor predictions for 3-year survival among HIV-associated and disseminated cryptococcosis involving lungs and central nervous system.

Antiretroviral and antifungal drug therapies Disseminated cryptococcosis HIV/AIDS Three-year survival-related predictions

Journal

Infection
ISSN: 1439-0973
Titre abrégé: Infection
Pays: Germany
ID NLM: 0365307

Informations de publication

Date de publication:
13 Apr 2024
Historique:
received: 16 11 2023
accepted: 13 03 2024
medline: 13 4 2024
pubmed: 13 4 2024
entrez: 13 4 2024
Statut: aheadofprint

Résumé

The global mortality rate resulting from HIV-associated cryptococcal disease is remarkably elevated, particularly in severe cases with dissemination to the lungs and central nervous system (CNS). Regrettably, there is a dearth of predictive analysis regarding long-term survival, and few studies have conducted longitudinal follow-up assessments for comparing anti-HIV and antifungal treatments. A cohort of 83 patients with HIV-related disseminated cryptococcosis involving the lung and CNS was studied for 3 years to examine survival. Comparative analysis of clinical and immunological parameters was performed between deceased and surviving individuals. Subsequently, multivariate Cox regression models were utilized to validate mortality predictions at 12, 24, and 36 months. Observed plasma cytokine levels before treatment were significantly lower for IL-1RA (p < 0.001) and MCP-1 (p < 0.05) when in the survivor group. Incorporating plasma levels of IL-1RA, IL-6, and high-risk CURB-65 score demonstrated the highest area under curve (AUC) value (0.96) for predicting 1-year mortality. For 1-, 2- and 3-year predictions, the single-factor model with IL-1RA demonstrated superior performance compared to all multiple-variate models (AUC = 0.95/0.78/0.78). IL-1RA is a biomarker for predicting 3-year survival. Further investigations to explore the pathogenetic role of IL-1RA in HIV-associated disseminated cryptococcosis and as a potential therapeutic target are warranted.

Sections du résumé

BACKGROUND BACKGROUND
The global mortality rate resulting from HIV-associated cryptococcal disease is remarkably elevated, particularly in severe cases with dissemination to the lungs and central nervous system (CNS). Regrettably, there is a dearth of predictive analysis regarding long-term survival, and few studies have conducted longitudinal follow-up assessments for comparing anti-HIV and antifungal treatments.
METHODS METHODS
A cohort of 83 patients with HIV-related disseminated cryptococcosis involving the lung and CNS was studied for 3 years to examine survival. Comparative analysis of clinical and immunological parameters was performed between deceased and surviving individuals. Subsequently, multivariate Cox regression models were utilized to validate mortality predictions at 12, 24, and 36 months.
RESULTS RESULTS
Observed plasma cytokine levels before treatment were significantly lower for IL-1RA (p < 0.001) and MCP-1 (p < 0.05) when in the survivor group. Incorporating plasma levels of IL-1RA, IL-6, and high-risk CURB-65 score demonstrated the highest area under curve (AUC) value (0.96) for predicting 1-year mortality. For 1-, 2- and 3-year predictions, the single-factor model with IL-1RA demonstrated superior performance compared to all multiple-variate models (AUC = 0.95/0.78/0.78).
CONCLUSIONS CONCLUSIONS
IL-1RA is a biomarker for predicting 3-year survival. Further investigations to explore the pathogenetic role of IL-1RA in HIV-associated disseminated cryptococcosis and as a potential therapeutic target are warranted.

Identifiants

pubmed: 38613657
doi: 10.1007/s15010-024-02237-6
pii: 10.1007/s15010-024-02237-6
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Shanghai Public Health Clinical Center
ID : KY-GW-2023-07
Organisme : Science and Technology Commission of Shanghai Municipality
ID : 20MC1920100
Organisme : Science and Technology Commission of Shanghai Municipality
ID : 21Y11901200

Informations de copyright

© 2024. The Author(s).

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Auteurs

Luling Wu (L)

Institute of Antibiotics, Huashan Hospital, Fudan University, Shanghai, China.
Department of Infectious Diseases and Immunology, Shanghai Public Health Clinical Center, Fudan University, Shanghai, China.

Xuemin Fu (X)

Research Group Statistical Genetics, Max Planck Institute of Psychiatry, Munich, Germany.

Benno Pütz (B)

Research Group Statistical Genetics, Max Planck Institute of Psychiatry, Munich, Germany.

Renfang Zhang (R)

Institute of Antibiotics, Huashan Hospital, Fudan University, Shanghai, China.

Li Liu (L)

Institute of Antibiotics, Huashan Hospital, Fudan University, Shanghai, China.

Wei Song (W)

Institute of Antibiotics, Huashan Hospital, Fudan University, Shanghai, China.

Ling Weng (L)

Department of Respiratory Medicine, Fuzhou Pulmonary Hospital, Fuzhou, Fujian, China.

Yueming Shao (Y)

Institute of Antibiotics, Huashan Hospital, Fudan University, Shanghai, China.

Zhihang Zheng (Z)

Institute of Antibiotics, Huashan Hospital, Fudan University, Shanghai, China.

Jingna Xun (J)

Institute of Antibiotics, Huashan Hospital, Fudan University, Shanghai, China.

Ximei Han (X)

Department of Respiratory Medicine, Fuzhou Pulmonary Hospital, Fuzhou, Fujian, China.

Ting Wang (T)

Department of Respiratory Medicine, Fuzhou Pulmonary Hospital, Fuzhou, Fujian, China.

Yinzhong Shen (Y)

Institute of Antibiotics, Huashan Hospital, Fudan University, Shanghai, China.

Hongzhou Lu (H)

Department of Infectious Diseases and Nursing Research Institution, National Clinical Research Center for Infectious Diseases, The Third People's Hospital of Shenzhen, Shenzhen, China.

Bertram Müller-Myhsok (B)

Research Group Statistical Genetics, Max Planck Institute of Psychiatry, Munich, Germany. bmm@psych.mpg.de.

Jun Chen (J)

Institute of Antibiotics, Huashan Hospital, Fudan University, Shanghai, China. qtchenjun@163.com.

Classifications MeSH