Dengue viremia kinetics and effects on platelet count and clinical outcomes: An analysis of 2340 patients from Vietnam.


Journal

eLife
ISSN: 2050-084X
Titre abrégé: Elife
Pays: England
ID NLM: 101579614

Informations de publication

Date de publication:
21 Jun 2024
Historique:
medline: 21 6 2024
pubmed: 21 6 2024
entrez: 21 6 2024
Statut: epublish

Résumé

Viremia is a critical factor in understanding the pathogenesis of dengue infection, but limited data exist on viremia kinetics. This study aimed to investigate the kinetics of viremia and its effects on subsequent platelet count, severe dengue, and plasma leakage. We pooled data from three studies conducted in Vietnam between 2000 and 2016, involving 2340 dengue patients with daily viremia measurements and platelet counts after symptom onset. Viremia kinetics were assessed using a random effects model that accounted for left-censored data. The effects of viremia on subsequent platelet count and clinical outcomes were examined using a landmark approach with a random effects model and logistic regression model with generalized estimating equations, respectively. The rate of viremia decline was derived from the model of viremia kinetics. Its effect on the clinical outcomes was assessed by logistic regression models. Viremia levels rapidly decreased following symptom onset, with variations observed depending on the infecting serotype. DENV-1 exhibited the highest mean viremia levels during the first 5-6 days, while DENV-4 demonstrated the shortest clearance time. Higher viremia levels were associated with decreased subsequent platelet counts from day 6 onwards. Elevated viremia levels on each illness day increased the risk of developing severe dengue and plasma leakage. However, the effect size decreased with later illness days. A more rapid decline in viremia is associated with a reduced risk of the clinical outcomes. This study provides comprehensive insights into viremia kinetics and its effect on subsequent platelet count and clinical outcomes in dengue patients. Our findings underscore the importance of measuring viremia levels during the early febrile phase for dengue studies and support the use of viremia kinetics as outcome for phase-2 dengue therapeutic trials. Wellcome Trust and European Union Seventh Framework Programme.

Sections du résumé

Background UNASSIGNED
Viremia is a critical factor in understanding the pathogenesis of dengue infection, but limited data exist on viremia kinetics. This study aimed to investigate the kinetics of viremia and its effects on subsequent platelet count, severe dengue, and plasma leakage.
Methods UNASSIGNED
We pooled data from three studies conducted in Vietnam between 2000 and 2016, involving 2340 dengue patients with daily viremia measurements and platelet counts after symptom onset. Viremia kinetics were assessed using a random effects model that accounted for left-censored data. The effects of viremia on subsequent platelet count and clinical outcomes were examined using a landmark approach with a random effects model and logistic regression model with generalized estimating equations, respectively. The rate of viremia decline was derived from the model of viremia kinetics. Its effect on the clinical outcomes was assessed by logistic regression models.
Results UNASSIGNED
Viremia levels rapidly decreased following symptom onset, with variations observed depending on the infecting serotype. DENV-1 exhibited the highest mean viremia levels during the first 5-6 days, while DENV-4 demonstrated the shortest clearance time. Higher viremia levels were associated with decreased subsequent platelet counts from day 6 onwards. Elevated viremia levels on each illness day increased the risk of developing severe dengue and plasma leakage. However, the effect size decreased with later illness days. A more rapid decline in viremia is associated with a reduced risk of the clinical outcomes.
Conclusions UNASSIGNED
This study provides comprehensive insights into viremia kinetics and its effect on subsequent platelet count and clinical outcomes in dengue patients. Our findings underscore the importance of measuring viremia levels during the early febrile phase for dengue studies and support the use of viremia kinetics as outcome for phase-2 dengue therapeutic trials.
Funding UNASSIGNED
Wellcome Trust and European Union Seventh Framework Programme.

Identifiants

pubmed: 38904662
doi: 10.7554/eLife.92606
pii: 92606
doi:
pii:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Wellcome Trust
ID : 084368/Z/07/Z
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 077078/Z/05/Z
Pays : United Kingdom
Organisme : European Union Seventh Framework Programme
ID : FP7-281803 IDAMS
Organisme : Wellcome Trust
ID : 106680/Z/14/Z
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 077078/Z/05/A
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 089276/B/09/Z
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 225167/Z/22/Z
Pays : United Kingdom

Informations de copyright

© 2024, Vuong et al.

Déclaration de conflit d'intérêts

NV, NQ, NT, KD, HD, PL, DT, TV, CS, RG No competing interests declared, TJ reports receiving personal fees as members of the Roche Pharmaceuticals Advisory Board on Severe Dengue, outside the submitted work, SY reports receiving personal honorarium for attending the Novartis dengue drug ad board meeting and Takeda dengue education symposium, outside the submitted work, BW reports receiving personal fees (a) as a member of the Roche Advisory Board on Severe Dengue and (b) as a member of the Data Monitoring and Adjudication Committees for the Takeda dengue vaccine trials, both outside the remit of the submitted work

Auteurs

Nguyen Lam Vuong (NL)

University of Medicine and Pharmacy at Ho Chi Minh City, Ho Chi Minh City, Viet Nam.
Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.

Nguyen Than Ha Quyen (NTH)

Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.

Nguyen Thi Hanh Tien (NTH)

Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.

Kien Duong Thi Hue (K)

Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.

Huynh Thi Le Duyen (HTL)

Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.

Phung Khanh Lam (PK)

University of Medicine and Pharmacy at Ho Chi Minh City, Ho Chi Minh City, Viet Nam.
Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.

Dong Thi Hoai Tam (DTH)

Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.

Tran Van Ngoc (T)

Hospital for Tropical Diseases, Ho Chi Minh City, Viet Nam.

Thomas Jaenisch (T)

Center for Global Health, Colorado School of Public Health, Aurora, United States.
Heidelberg Institute of Global Health (HIGH), Heidelberg University Hospital, Heidelberg, Germany.

Cameron P Simmons (CP)

Centre for Tropical Medicine and Global health, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, United Kingdom.
World Mosquito Program, Monash University, Clayton, Australia.

Sophie Yacoub (S)

Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.
Centre for Tropical Medicine and Global health, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, United Kingdom.

Bridget A Wills (BA)

Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.
Centre for Tropical Medicine and Global health, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, United Kingdom.

Ronald Geskus (R)

Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.
Centre for Tropical Medicine and Global health, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, United Kingdom.

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