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dc.contributor.authorEtyang, A. O.
dc.contributor.authorWandabwa, C. K.
dc.contributor.authorKapesa, S.
dc.contributor.authorMuthumbi, E.
dc.contributor.authorOdipo, E.
dc.contributor.authorWamukoya, M.
dc.contributor.authorNgomi, Nicholas N.
dc.contributor.authorHaregu, T.
dc.contributor.authorKyobutungi, C.
dc.contributor.authorWilliams, T. N.
dc.contributor.authorMakale, J.
dc.contributor.authorMacharia, A.
dc.contributor.authorCruickshank, J. K.
dc.contributor.authorSmeeth, L.
dc.contributor.authorScott, A. G.
dc.date.accessioned2021-03-22T14:00:39Z
dc.date.available2021-03-22T14:00:39Z
dc.date.issued2017-05-22
dc.identifier.citationAmerican Journal of Epidemiology, 2018;187(2):199–205en_US
dc.identifier.urihttps://pubmed.ncbi.nlm.nih.gov/28992220/
dc.identifier.urihttps://academic.oup.com/aje/article/187/2/199/3867261
dc.identifier.urihttps://www.researchgate.net/publication/317582785_Blood_Pressure_and_Arterial_Stiffness_in_Kenyan_Adolescents_With_the_Sickle_Cell_Trait
dc.identifier.urihttps://researchonline.lshtm.ac.uk/id/eprint/4503991/1/Blood%20Pressure%20and%20Arterial%20Stiffness_GREEN%20AAM.pdf
dc.identifier.urihttps://www.ndm.ox.ac.uk/publications/835540
dc.identifier.urihttps://www.x-mol.com/paper/1213019116239261723?recommend
dc.identifier.urihttps://www.semanticscholar.org/paper/Blood-Pressure-and-Arterial-Stiffness-in-Kenyan-the-Etyang-Wandabwa/dea8035877cd06c25607d77293568d0db1a99413
dc.identifier.urihttp://hdl.handle.net/123456789/4550
dc.identifier.uriBlood Pressure and Arterial Stiffness in Kenyan Adolescents With the Sickle Cell Trait
dc.description.abstractThe potential association between sickle cell trait (SCT) and increased arterial stiffness/blood pressure (BP) has not been evaluated in detail despite its association with stroke, sudden death, and renal disease. We performed 24-hour ambulatory BP monitoring and arterial stiffness measurements in adolescents raised in a malaria-free environment in Kenya. Between December 2015 and June 2016, 938 randomly selected adolescents (ages 11-17 years) who had been continuous residents of Nairobi from birth were invited to participate in the study. Standard clinic BP measurement was performed, followed by 24-hour ambulatory BP monitoring and arterial stiffness measurement using an Arteriograph24 (TensioMed Ltd., Budapest, Hungary) device. SCT status was determined using DNA genotyping in contemporaneously collected blood samples. Of the 938 adolescents invited to participate, 609 (65%) provided complete data for analysis. SCT was present in 103 (15%). Mean 24-hour systolic and diastolic BPs were 116 (standard deviation (SD), 11.5) mm Hg and 64 (SD, 7) mm Hg, respectively, in children with SCT and 117 (SD, 11.4) mm Hg and 64 (SD, 6.8) mm Hg, respectively, in non-SCT children. Mean pulse wave velocity (PWV) was 7.1 (SD, 0.8) m/second and 7.0 (SD, 0.8) m/second in SCT and non-SCT children, respectively. We observed no differences in PWV or in any clinic or ambulatory BP-derived measures between adolescents with and without SCT. These data suggest that SCT does not independently influence BP or PWV.en_US
dc.language.isoenen_US
dc.subjectSickle cell trait; Hypertension; Blood Pressure; Arterial Stiffnessen_US
dc.titleBlood Pressure and Arterial Stiffness in Kenyan Adolescents With the Sickle Cell Traiten_US
dc.typeArticleen_US


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