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Homozygote drepanocytosis: Ferric status and inflammation in world and Africa: Review article and meta analysis
BACKGROUND AND AIMS: Major sickle cell syndromes are subjected to a high frequency of hemolysis, infections, oxidative stress, and vasooclusive crises which promote inflammation and iron balance disorders. We aimed to systematically review and analyze the studies in this patients addressing in gener...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10551275/ https://www.ncbi.nlm.nih.gov/pubmed/37808933 http://dx.doi.org/10.1002/hsr2.1609 |
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author | Tuono De Manfouo, Romaric Louokdom, Josué Simo Chetcha, Bernard Claude Nya, Prosper Cabral Biapa Pieme, Constant Anatole Tagny, Claude Tayou |
author_facet | Tuono De Manfouo, Romaric Louokdom, Josué Simo Chetcha, Bernard Claude Nya, Prosper Cabral Biapa Pieme, Constant Anatole Tagny, Claude Tayou |
author_sort | Tuono De Manfouo, Romaric |
collection | PubMed |
description | BACKGROUND AND AIMS: Major sickle cell syndromes are subjected to a high frequency of hemolysis, infections, oxidative stress, and vasooclusive crises which promote inflammation and iron balance disorders. We aimed to systematically review and analyze the studies in this patients addressing in general, and Africa in particular. METHODS: The systematic review of published articles in the Pubmed and Google Scholar databases was carried out according to the recommendations of the PRISMA model. The case‐control articles have been included. The data extracted from the articles were analyzed using statistical software R. The standardized mean difference (SMD) was used to assess the extent of the disease on the different variables studied. RESULTS: At the end, 128 articles were obtained; but only 33 were elligible for meta‐analysis. A SMD of −1.79 was obtained for hemoglobin between the sickle cell patients and the controls due to the deviation from the overall mean hemoglobin in the cases (8 ± 2 g/dL) and in controls (13 ± 3 g/dL). Sickle cell disease showed a significant extent on ferritin [SMD = 2.61; (95% confidence interval, CI: 2.39–2.83); (p < 0.01)] compared to non‐sickle cell patients thus describing a higher risk for sickle cell sufferer to have ferritin disorders. The included studies also described the influence of sickle cell anemia on serum iron [SMD = 1.52; (95% CI: 1.32–1.76); (p < 0.01)] compared to normal subjects. The high risk of inflammation has been described as higher in sickle cell patients [SMD = 0.38; (95% CI: 0.25–0.50)], reflecting the moderate extent of sickle cell disease on inflammation. CONCLUSION: Patients with major sickle cell syndrome in inflammation have a higher risk of iron profile disorders compared to the normal population. Further studies are needed to explore mechanisms for preventing the deleterious effects of iron from this hemolysis, for example haptoglobin genotyping. |
format | Online Article Text |
id | pubmed-10551275 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-105512752023-10-06 Homozygote drepanocytosis: Ferric status and inflammation in world and Africa: Review article and meta analysis Tuono De Manfouo, Romaric Louokdom, Josué Simo Chetcha, Bernard Claude Nya, Prosper Cabral Biapa Pieme, Constant Anatole Tagny, Claude Tayou Health Sci Rep Narrative Review BACKGROUND AND AIMS: Major sickle cell syndromes are subjected to a high frequency of hemolysis, infections, oxidative stress, and vasooclusive crises which promote inflammation and iron balance disorders. We aimed to systematically review and analyze the studies in this patients addressing in general, and Africa in particular. METHODS: The systematic review of published articles in the Pubmed and Google Scholar databases was carried out according to the recommendations of the PRISMA model. The case‐control articles have been included. The data extracted from the articles were analyzed using statistical software R. The standardized mean difference (SMD) was used to assess the extent of the disease on the different variables studied. RESULTS: At the end, 128 articles were obtained; but only 33 were elligible for meta‐analysis. A SMD of −1.79 was obtained for hemoglobin between the sickle cell patients and the controls due to the deviation from the overall mean hemoglobin in the cases (8 ± 2 g/dL) and in controls (13 ± 3 g/dL). Sickle cell disease showed a significant extent on ferritin [SMD = 2.61; (95% confidence interval, CI: 2.39–2.83); (p < 0.01)] compared to non‐sickle cell patients thus describing a higher risk for sickle cell sufferer to have ferritin disorders. The included studies also described the influence of sickle cell anemia on serum iron [SMD = 1.52; (95% CI: 1.32–1.76); (p < 0.01)] compared to normal subjects. The high risk of inflammation has been described as higher in sickle cell patients [SMD = 0.38; (95% CI: 0.25–0.50)], reflecting the moderate extent of sickle cell disease on inflammation. CONCLUSION: Patients with major sickle cell syndrome in inflammation have a higher risk of iron profile disorders compared to the normal population. Further studies are needed to explore mechanisms for preventing the deleterious effects of iron from this hemolysis, for example haptoglobin genotyping. John Wiley and Sons Inc. 2023-10-04 /pmc/articles/PMC10551275/ /pubmed/37808933 http://dx.doi.org/10.1002/hsr2.1609 Text en © 2023 The Authors. Health Science Reports published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Narrative Review Tuono De Manfouo, Romaric Louokdom, Josué Simo Chetcha, Bernard Claude Nya, Prosper Cabral Biapa Pieme, Constant Anatole Tagny, Claude Tayou Homozygote drepanocytosis: Ferric status and inflammation in world and Africa: Review article and meta analysis |
title | Homozygote drepanocytosis: Ferric status and inflammation in world and Africa: Review article and meta analysis |
title_full | Homozygote drepanocytosis: Ferric status and inflammation in world and Africa: Review article and meta analysis |
title_fullStr | Homozygote drepanocytosis: Ferric status and inflammation in world and Africa: Review article and meta analysis |
title_full_unstemmed | Homozygote drepanocytosis: Ferric status and inflammation in world and Africa: Review article and meta analysis |
title_short | Homozygote drepanocytosis: Ferric status and inflammation in world and Africa: Review article and meta analysis |
title_sort | homozygote drepanocytosis: ferric status and inflammation in world and africa: review article and meta analysis |
topic | Narrative Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10551275/ https://www.ncbi.nlm.nih.gov/pubmed/37808933 http://dx.doi.org/10.1002/hsr2.1609 |
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