| Literature DB >> 26820850 |
Kavita Gandhi, Mahamadou A Thera, Drissa Coulibaly, Karim Traoré, Ando B Guindo, Amed Ouattara, Shannon Takala-Harrison, Andrea A Berry, Ogobara K Doumbo, Christopher V Plowe.
Abstract
[This corrects the article DOI: 10.1371/journal.pone.0101783.].Entities:
Year: 2016 PMID: 26820850 PMCID: PMC4731568 DOI: 10.1371/journal.pone.0148240
Source DB: PubMed Journal: PLoS One ISSN: 1932-6203 Impact factor: 3.240
Fig 5Association between change in the predominant amino at a polymorphic site and the hazard of Plasmodium falciparum clinical disease.
The association between changes at polymorphic sites in Th2R and Th3R which occurred between consecutive clinical episodes and the hazard of clinical disease was calculated using a Cox proportional hazards model. To account for the possibility of treatment failure and to allow for time for allele-specific antibodies to the first of two paired consecutive infections to be present by the time of the second infection, time intervals two weeks or less between consecutive episodes were excluded from the analyses. No significant association between changes at polymorphic sites in Th2R and Th3R which occurred between a clinical episode and a consecutive asymptomatic infection and the hazard of clinical disease was found. Asterisks denote polymorphic amino acid positions that lacked power to detect a hazard ratio below 1.51.
Fig 6Association between change in the predominant amino at a polymorphic site and the hazard of Plasmodium falciparum infection.
The association between changes at polymorphic sites in Th2R and Th3R which occurred between consecutive clinical episodes and the hazard of infection was calculated using a Cox proportional hazards model. To account for the possibility of treatment failure and to allow for time for allele-specific antibodies to the first of two paired consecutive infections to be present by the time of the second infection, time intervals two weeks or less between consecutive episodes were excluded from the analyses. No significant association between changes at polymorphic sites in Th2R and Th3R which occurred between consecutive clinical episodes and the hazard of infection was found. Asterisks denote polymorphic amino acid positions that lacked power to detect a hazard ratio below 1.51.