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Study of C reactive protein as a prognostic marker in malaria from Eastern India
BACKGROUND: C-reactive protein (CRP) is useful as marker of severity in malaria. African studies have shown that serum CRP levels correlate with parasite burden and complications in malaria, especially falciparum. However, there are very few data on CRP levels in Indian malaria patients. MATERIALS A...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3544111/ https://www.ncbi.nlm.nih.gov/pubmed/23326772 http://dx.doi.org/10.4103/2277-9175.100140 |
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author | Paul, Rudrajit Sinha, Pradip K. Bhattacharya, Raja Banerjee, Amit K. Raychaudhuri, Pradip Mondal, Jayati |
author_facet | Paul, Rudrajit Sinha, Pradip K. Bhattacharya, Raja Banerjee, Amit K. Raychaudhuri, Pradip Mondal, Jayati |
author_sort | Paul, Rudrajit |
collection | PubMed |
description | BACKGROUND: C-reactive protein (CRP) is useful as marker of severity in malaria. African studies have shown that serum CRP levels correlate with parasite burden and complications in malaria, especially falciparum. However, there are very few data on CRP levels in Indian malaria patients. MATERIALS AND METHODS: We assessed CRP levels in malaria patients at presentation and studied for any relation of CRP levels with subsequent prognosis. Statistical tests included student's t-test, Mann Whitney U test, and chi square test, all with 2-tailed analyzes. RESULTS: Of 71 patients in our study, 42 (59.1%) were infected with P. falciparum. 23 (32.4%) patients needed admission and 10 (14.1%) died. Average CRP levels were quite high in malaria patients (31.29 ± 20.4 mg/L). There was no significant difference in CRP between vivax and falciparum cases. Admitted patients had significantly higher CRP levels compared to those treated on outdoor basis (47.11 ± 19.13 vs. 23.71 ± 16.35 mg/L; P < 0.0001). 8 patients were admitted with multiple complications. They had significantly high CRP level compared to those with 1 complication (P = 0.015). Also, patients who died had higher CRP levels compared to survivors (P = 0.000346). CRP levels at presentation showed positive correlation with duration of hospital stay (r = 0.59; P < 0.05). CRP levels >35 mg/L was highly sensitive in predicting mortality. CONCLUSION: Our study in Indian population corroborates the findings in African studies regarding prognostic role of CRP in malaria. CRP is an effective biomarker in assessing malaria severity and also for follow-up. |
format | Online Article Text |
id | pubmed-3544111 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-35441112013-01-16 Study of C reactive protein as a prognostic marker in malaria from Eastern India Paul, Rudrajit Sinha, Pradip K. Bhattacharya, Raja Banerjee, Amit K. Raychaudhuri, Pradip Mondal, Jayati Adv Biomed Res Original Article BACKGROUND: C-reactive protein (CRP) is useful as marker of severity in malaria. African studies have shown that serum CRP levels correlate with parasite burden and complications in malaria, especially falciparum. However, there are very few data on CRP levels in Indian malaria patients. MATERIALS AND METHODS: We assessed CRP levels in malaria patients at presentation and studied for any relation of CRP levels with subsequent prognosis. Statistical tests included student's t-test, Mann Whitney U test, and chi square test, all with 2-tailed analyzes. RESULTS: Of 71 patients in our study, 42 (59.1%) were infected with P. falciparum. 23 (32.4%) patients needed admission and 10 (14.1%) died. Average CRP levels were quite high in malaria patients (31.29 ± 20.4 mg/L). There was no significant difference in CRP between vivax and falciparum cases. Admitted patients had significantly higher CRP levels compared to those treated on outdoor basis (47.11 ± 19.13 vs. 23.71 ± 16.35 mg/L; P < 0.0001). 8 patients were admitted with multiple complications. They had significantly high CRP level compared to those with 1 complication (P = 0.015). Also, patients who died had higher CRP levels compared to survivors (P = 0.000346). CRP levels at presentation showed positive correlation with duration of hospital stay (r = 0.59; P < 0.05). CRP levels >35 mg/L was highly sensitive in predicting mortality. CONCLUSION: Our study in Indian population corroborates the findings in African studies regarding prognostic role of CRP in malaria. CRP is an effective biomarker in assessing malaria severity and also for follow-up. Medknow Publications & Media Pvt Ltd 2012-08-28 /pmc/articles/PMC3544111/ /pubmed/23326772 http://dx.doi.org/10.4103/2277-9175.100140 Text en Copyright: © 2012 Paul http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Original Article Paul, Rudrajit Sinha, Pradip K. Bhattacharya, Raja Banerjee, Amit K. Raychaudhuri, Pradip Mondal, Jayati Study of C reactive protein as a prognostic marker in malaria from Eastern India |
title | Study of C reactive protein as a prognostic marker in malaria from Eastern India |
title_full | Study of C reactive protein as a prognostic marker in malaria from Eastern India |
title_fullStr | Study of C reactive protein as a prognostic marker in malaria from Eastern India |
title_full_unstemmed | Study of C reactive protein as a prognostic marker in malaria from Eastern India |
title_short | Study of C reactive protein as a prognostic marker in malaria from Eastern India |
title_sort | study of c reactive protein as a prognostic marker in malaria from eastern india |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3544111/ https://www.ncbi.nlm.nih.gov/pubmed/23326772 http://dx.doi.org/10.4103/2277-9175.100140 |
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