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C-reactive protein as a potential biomarker for disease progression in dengue: a multi-country observational study.
Vuong, Nguyen Lam; Le Duyen, Huynh Thi; Lam, Phung Khanh; Tam, Dong Thi Hoai; Vinh Chau, Nguyen Van; Van Kinh, Nguyen; Chanpheaktra, Ngoun; Lum, Lucy Chai See; Pleités, Ernesto; Jones, Nick Keith; Simmons, Cameron Paul; Rosenberger, Kerstin; Jaenisch, Thomas; Halleux, Christine; Olliaro, Piero Luigi; Wills, Bridget; Yacoub, Sophie.
Affiliation
  • Vuong NL; Oxford University Clinical Research Unit, Wellcome Trust Asia Programme, Ho Chi Minh City, Vietnam.
  • Le Duyen HT; University of Medicine and Pharmacy at Ho Chi Minh City, Ho Chi Minh City, Vietnam.
  • Lam PK; Oxford University Clinical Research Unit, Wellcome Trust Asia Programme, Ho Chi Minh City, Vietnam.
  • Tam DTH; Oxford University Clinical Research Unit, Wellcome Trust Asia Programme, Ho Chi Minh City, Vietnam.
  • Vinh Chau NV; Oxford University Clinical Research Unit, Wellcome Trust Asia Programme, Ho Chi Minh City, Vietnam.
  • Van Kinh N; Hospital of Tropical Diseases, Ho Chi Minh City, Vietnam.
  • Chanpheaktra N; National Hospital for Tropical Diseases (NHTD), Hanoi, Vietnam.
  • Lum LCS; Angkor Hospital for Children, Siem Reap, Cambodia.
  • Pleités E; University of Malaya Medical Centre, Kuala Lumpur, Malaysia.
  • Jones NK; Hospital Nacional de Niños Benjamin Bloom, San Salvador, El Salvador.
  • Simmons CP; University of Cambridge, Cambridge, UK.
  • Rosenberger K; Oxford University Clinical Research Unit, Wellcome Trust Asia Programme, Ho Chi Minh City, Vietnam.
  • Jaenisch T; Institute of Vector-Borne Disease, Monash University, Melbourne, Australia.
  • Halleux C; Section of Clinical Tropical Medicine, Department of Infectious Diseases, Heidelberg University Hospital, Heidelberg, Germany.
  • Olliaro PL; Section of Clinical Tropical Medicine, Department of Infectious Diseases, Heidelberg University Hospital, Heidelberg, Germany.
  • Wills B; UNICEF/UNDP/World Bank/WHO Special Programme for Research and Training in Tropical Diseases, World Health Organization, Geneva, Switzerland.
  • Yacoub S; Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
BMC Med ; 18(1): 35, 2020 02 17.
Article in En | MEDLINE | ID: mdl-32063229
ABSTRACT

BACKGROUND:

Dengue infection can cause a wide spectrum of clinical outcomes. The severe clinical manifestations occur sufficiently late in the disease course, during day 4-6 of illness, to allow a window of opportunity for risk stratification. Markers of inflammation may be useful biomarkers. We investigated the value of C-reactive protein (CRP) measured early on illness days 1-3 to predict dengue disease outcome and the difference in CRP levels between dengue and other febrile illnesses (OFI).

METHOD:

We performed a nested case-control study using the clinical data and samples collected from the IDAMS-consortium multi-country study. This was a prospective multi-center observational study that enrolled almost 8000 participants presenting with a dengue-like illness to outpatient facilities in 8 countries across Asia and Latin America. Predefined severity definitions of severe and intermediate dengue were used as the primary outcomes. A total of 281 cases with severe/intermediate dengue were compared to 836 uncomplicated dengue patients as controls (ratio 13), and also 394 patients with OFI.

RESULTS:

In patients with confirmed dengue, median (interquartile range) of CRP level within the first 3 days was 30.2 mg/L (12.4-61.2 mg/L) (uncomplicated dengue, 28.6 (10.5-58.9); severe or intermediate dengue, 34.0 (17.4-71.8)). Higher CRP levels in the first 3 days of illness were associated with a higher risk of severe or intermediate outcome (OR 1.17, 95% CI 1.07-1.29), especially in children. Higher CRP levels, exceeding 30 mg/L, also associated with hospitalization (OR 1.37, 95% CI 1.14-1.64) and longer fever clearance time (HR 0.84, 95% CI 0.76-0.93), especially in adults. CRP levels in patients with dengue were higher than patients with potential viral infection but lower than patients with potential bacterial infection, resulting in a quadratic association between dengue diagnosis and CRP, with levels of approximately 30 mg/L associated with the highest risk of having dengue. CRP had a positive correlation with total white cell count and neutrophils and negative correlation with lymphocytes, but did not correlate with liver transaminases, albumin, or platelet nadir.

CONCLUSIONS:

In summary, CRP measured in the first 3 days of illness could be a useful biomarker for early dengue risk prediction and may assist differentiating dengue from other febrile illnesses.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: C-Reactive Protein / Biomarkers / Severe Dengue Type of study: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Language: En Journal: BMC Med Journal subject: MEDICINA Year: 2020 Type: Article Affiliation country: Vietnam

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: C-Reactive Protein / Biomarkers / Severe Dengue Type of study: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Language: En Journal: BMC Med Journal subject: MEDICINA Year: 2020 Type: Article Affiliation country: Vietnam