| Literature DB >> 24957539 |
Tamar E Carter1, Michael von Fricken2, Jean R Romain2, Gladys Memnon2, Yves St Victor2, Laura Schick2, Bernard A Okech2, Connie J Mulligan2.
Abstract
Sickle cell disease is a growing global health concern because infants born with the disorder in developing countries are now surviving longer with little access to diagnostic and management options. In Haiti, the current state of sickle cell disease/trait in the population is unclear. To inform future screening efforts in Haiti, we assayed sickle hemoglobin mutations using traditional hemoglobin solubility tests (HST) and add-on techniques, which incorporated spectrophotometry and insoluble hemoglobin separation. We also generated genotype data as a metric for HST performance. We found 19 of 202 individuals screened with HST were positive for sickle hemoglobin, five of whom did not carry the HbS allele. We show that spectrophotometry and insoluble hemoglobin separation add-on techniques could resolve false positives associated with the traditional HST approach, with some limitations. We also discuss the incorporation of insoluble hemoglobin separation observation with HST in suboptimal screening settings like Haiti. © The American Society of Tropical Medicine and Hygiene.Entities:
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Year: 2014 PMID: 24957539 PMCID: PMC4125270 DOI: 10.4269/ajtmh.13-0572
Source DB: PubMed Journal: Am J Trop Med Hyg ISSN: 0002-9637 Impact factor: 2.345