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Racial Variations in the Markers of Mineral Bone Disorders in CKD Patients in South Africa

INTRODUCTION: Several studies showed that serum intact parathyroid hormone (PTH), phosphate, and vitamin D levels differ across races. These comparative studies were largely carried out between Caucasians and black Americans. However, little is known of the existence of these associations in an Afri...

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Autores principales: Waziri, Bala, Duarte, Raquel, Dickens, Caroline, Dix Peek, Therese, George, Jaya, Rekhviashvili, Vakhtang, Paget, Graham, Naicker, Saraladevi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5976813/
https://www.ncbi.nlm.nih.gov/pubmed/29854965
http://dx.doi.org/10.1016/j.ekir.2017.12.004
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author Waziri, Bala
Duarte, Raquel
Dickens, Caroline
Dix Peek, Therese
George, Jaya
Rekhviashvili, Vakhtang
Paget, Graham
Naicker, Saraladevi
author_facet Waziri, Bala
Duarte, Raquel
Dickens, Caroline
Dix Peek, Therese
George, Jaya
Rekhviashvili, Vakhtang
Paget, Graham
Naicker, Saraladevi
author_sort Waziri, Bala
collection PubMed
description INTRODUCTION: Several studies showed that serum intact parathyroid hormone (PTH), phosphate, and vitamin D levels differ across races. These comparative studies were largely carried out between Caucasians and black Americans. However, little is known of the existence of these associations in an African population with chronic kidney disease (CKD). METHODS: This cross-sectional multicenter study involved 293 CKD patients from 3 renal units in Johannesburg, South Africa. RESULTS: The 293 CKD patients (208 blacks, 85 whites) had an overall mean age of 51.1 ± 13.6 years, and black patients were significantly younger than the white patients (48.4 ± 13.6 years vs. 57.1 ± 15.5 years; P < 0.001). Compared with whites, blacks had higher median intact PTH (498 [range: 37–1084] pg/ml vs. 274 [range: 131–595] pg/ml; P = 0.03), alkaline phosphatase (122 [range: 89–192] U/L vs. 103 [range: 74–144] U/L; p = 0.03), and mean 25 OH vitamin D(3) (26.8 ± 12.7 ng/ml vs. 22.7 ± 12.2 ng/ml, P = 0.01) levels, whereas their median fibroblast growth factor (FGF) level was 23 (100 [range: 34–639] pg/ml vs. 233 [range: 80–1370] pg/ml; P = 0.002), and their mean serum phosphate (1.3 ± 0.5 vs. 1.5 ± 0.5; P = 0.001) levels were significantly lower. In multivariable analyses, black race was independently associated with increased log PTH (β = 0.488, P = 0.01) and decreased log FGF-23 (β = −0.636, P = 0.02). Similarly, blacks had a 3.08 times higher likelihood (95% confidence interval: 1.51–6.30; P = 0.002) of developing severe hyperparathyroidism than whites. CONCLUSION: This study highlighted the existence of racial differences in the circulating markers of mineral bone disorders in an African CKD population.
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spelling pubmed-59768132018-05-31 Racial Variations in the Markers of Mineral Bone Disorders in CKD Patients in South Africa Waziri, Bala Duarte, Raquel Dickens, Caroline Dix Peek, Therese George, Jaya Rekhviashvili, Vakhtang Paget, Graham Naicker, Saraladevi Kidney Int Rep Clinical Research INTRODUCTION: Several studies showed that serum intact parathyroid hormone (PTH), phosphate, and vitamin D levels differ across races. These comparative studies were largely carried out between Caucasians and black Americans. However, little is known of the existence of these associations in an African population with chronic kidney disease (CKD). METHODS: This cross-sectional multicenter study involved 293 CKD patients from 3 renal units in Johannesburg, South Africa. RESULTS: The 293 CKD patients (208 blacks, 85 whites) had an overall mean age of 51.1 ± 13.6 years, and black patients were significantly younger than the white patients (48.4 ± 13.6 years vs. 57.1 ± 15.5 years; P < 0.001). Compared with whites, blacks had higher median intact PTH (498 [range: 37–1084] pg/ml vs. 274 [range: 131–595] pg/ml; P = 0.03), alkaline phosphatase (122 [range: 89–192] U/L vs. 103 [range: 74–144] U/L; p = 0.03), and mean 25 OH vitamin D(3) (26.8 ± 12.7 ng/ml vs. 22.7 ± 12.2 ng/ml, P = 0.01) levels, whereas their median fibroblast growth factor (FGF) level was 23 (100 [range: 34–639] pg/ml vs. 233 [range: 80–1370] pg/ml; P = 0.002), and their mean serum phosphate (1.3 ± 0.5 vs. 1.5 ± 0.5; P = 0.001) levels were significantly lower. In multivariable analyses, black race was independently associated with increased log PTH (β = 0.488, P = 0.01) and decreased log FGF-23 (β = −0.636, P = 0.02). Similarly, blacks had a 3.08 times higher likelihood (95% confidence interval: 1.51–6.30; P = 0.002) of developing severe hyperparathyroidism than whites. CONCLUSION: This study highlighted the existence of racial differences in the circulating markers of mineral bone disorders in an African CKD population. Elsevier 2017-12-12 /pmc/articles/PMC5976813/ /pubmed/29854965 http://dx.doi.org/10.1016/j.ekir.2017.12.004 Text en © 2017 International Society of Nephrology. Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Clinical Research
Waziri, Bala
Duarte, Raquel
Dickens, Caroline
Dix Peek, Therese
George, Jaya
Rekhviashvili, Vakhtang
Paget, Graham
Naicker, Saraladevi
Racial Variations in the Markers of Mineral Bone Disorders in CKD Patients in South Africa
title Racial Variations in the Markers of Mineral Bone Disorders in CKD Patients in South Africa
title_full Racial Variations in the Markers of Mineral Bone Disorders in CKD Patients in South Africa
title_fullStr Racial Variations in the Markers of Mineral Bone Disorders in CKD Patients in South Africa
title_full_unstemmed Racial Variations in the Markers of Mineral Bone Disorders in CKD Patients in South Africa
title_short Racial Variations in the Markers of Mineral Bone Disorders in CKD Patients in South Africa
title_sort racial variations in the markers of mineral bone disorders in ckd patients in south africa
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5976813/
https://www.ncbi.nlm.nih.gov/pubmed/29854965
http://dx.doi.org/10.1016/j.ekir.2017.12.004
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