TY - JOUR
T1 - Inducible nitric oxide synthase 2 promoterpolymorphism and malaria disease severity in children in Southern Ghana
AU - Dzodzomenyo, Mawuli
AU - Ghansah, Anita
AU - Ensaw, Nana
AU - Dovie, Benjamin
AU - Bimi, Langbong
AU - Quansah, Reginald
AU - Gyan, Ben A.
AU - Gyakobo, Mawuli
AU - Amoani, Benjamin
N1 - Publisher Copyright:
© 2018 Public Library of Science. All rights reserved.
PY - 2019/7/1
Y1 - 2019/7/1
N2 - Objective We assessed the association of mutant allele frequencies of nitric oxide synthase 2 (NOS2) gene at two SNPs (-954 and-1173) with malaria disease severity in children from a malaria endemic area in Southern Ghana.Method Using children recruited at the hospital, assigned into clinical subgroups of uncomplicated and severe malaria and matching with their "healthy control" counterparts, we designed a case control study. Genomic DNA was extracted and genotyping using Restriction Fragment Polymorphism was done. Result A total of 123 malaria cases (91 uncomplicated, 32 severe) and 100 controls were sampled. Their corresponding mean Hbs were 9.6, 9.3 and 11.2g/dl and geometric mean parasite densities of 32097, 193252 and 0 parasites/ml respectively. Variant allele frequencies varied from 0.09 through 0.03 to 0.12 for G-954C and 0.06 through 0.03 to 0.07 for C-1173T in the uncomplicated, severe and healthy control groups respectively. There was a strong linkage disequilibrium between the two alleles (p<0.001). For the-954 position, the odds of developing severe malaria was found to be 2.5 times lower with the carriage of a C allele compared to those without severe malaria (?2; p< 0.05) though this isn't the case with-1173. Conclusion The carriage of a mutant allele in the-954 NOS2 gene may have a protective effect on malaria among Southern Ghanaian children.
AB - Objective We assessed the association of mutant allele frequencies of nitric oxide synthase 2 (NOS2) gene at two SNPs (-954 and-1173) with malaria disease severity in children from a malaria endemic area in Southern Ghana.Method Using children recruited at the hospital, assigned into clinical subgroups of uncomplicated and severe malaria and matching with their "healthy control" counterparts, we designed a case control study. Genomic DNA was extracted and genotyping using Restriction Fragment Polymorphism was done. Result A total of 123 malaria cases (91 uncomplicated, 32 severe) and 100 controls were sampled. Their corresponding mean Hbs were 9.6, 9.3 and 11.2g/dl and geometric mean parasite densities of 32097, 193252 and 0 parasites/ml respectively. Variant allele frequencies varied from 0.09 through 0.03 to 0.12 for G-954C and 0.06 through 0.03 to 0.07 for C-1173T in the uncomplicated, severe and healthy control groups respectively. There was a strong linkage disequilibrium between the two alleles (p<0.001). For the-954 position, the odds of developing severe malaria was found to be 2.5 times lower with the carriage of a C allele compared to those without severe malaria (?2; p< 0.05) though this isn't the case with-1173. Conclusion The carriage of a mutant allele in the-954 NOS2 gene may have a protective effect on malaria among Southern Ghanaian children.
UR - http://www.scopus.com/inward/record.url?scp=85053807758&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0202218
DO - 10.1371/journal.pone.0202218
M3 - Article
C2 - 30118498
AN - SCOPUS:85053807758
SN - 1932-6203
VL - 13
JO - PLoS ONE
JF - PLoS ONE
IS - 8
M1 - e0202218
ER -