Genetic variants associated with dengue hemorrhagic fever. A systematic review and meta-analysis

Copyright © 2024 The Author(s). Published by Elsevier Ltd.. All rights reserved..

Dengue hemorrhagic fever (DHF) is a severe condition resulting from the dengue virus, with four serotypes known as DEN-1, DEN-2, DEN-3, and DEN-4. Genetic variations play a crucial role in influencing susceptibility to DHF. Therefore, this investigation conducted a meta-analysis to uncover genetic changes that might have remained undetected in individual studies due to small sample sizes or methodological differences. Among 2212 initially identified studies, 23 were deemed suitable for analysis based on PRISMA guidelines. Toll-like receptors (TLR) and CD209 showed significant association with DHF (odds ratios: TLR=0.56, CD209 =0.55), indicating protective effects. However, tumor necrosis factor (TNF) and human leukocyte antigen (HLA) did not exhibit a statistically significant relationship with DHF. This study emphasizes the relevance of TLR and CD209 in DHF susceptibility and resistance across diverse geographical locations.

Medienart:

E-Artikel

Erscheinungsjahr:

2024

Erschienen:

2024

Enthalten in:

Zur Gesamtaufnahme - volume:17

Enthalten in:

Journal of infection and public health - 17(2024), 4 vom: 22. März, Seite 579-587

Sprache:

Englisch

Beteiligte Personen:

Kanan, Mohammed [VerfasserIn]
Naffaa, Mohammed [VerfasserIn]
Alanazi, Ahmed [VerfasserIn]
Nasser, Faiz [VerfasserIn]
Alsaiari, Ahad Amer [VerfasserIn]
Almehmadi, Mazen [VerfasserIn]
Assiry, Ali [VerfasserIn]
Muzafar, Hisham [VerfasserIn]
Katam, Hejab [VerfasserIn]
Arar, Abdullah [VerfasserIn]
Asdaq, Syed Mohammed Basheeruddin [VerfasserIn]
Abida [VerfasserIn]
Imran, Mohd [VerfasserIn]
Dzinamarira, Tafadzwa [VerfasserIn]

Links:

Volltext

Themen:

Dengue virus
Human leukocyte antigen
Journal Article
Meta-Analysis
Meta-analysis
Odd ratio
Review
Systematic Review
TNF toll-like receptors
Tumor Necrosis Factor-alpha

Anmerkungen:

Date Completed 25.03.2024

Date Revised 25.03.2024

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1016/j.jiph.2024.02.001

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM36858707X