Two risk factors for hypozincemia in diabetic [beta]-thalassemia patients: Hepatitis C and deferasirox
Hypozincemia is a prevalent adverse consequence in diabetes mellitus (DM) and [beta]-Thalassemia patients. We aimed to evaluate the level of serum zinc in [beta]-thalassemia patients with DM and a risk assessment for hypozincemia. The study population included transfusion-dependent thalassemia (TDT)...
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creator | Darvishi-Khezri, Hadi Karami, Hossein Naderisorki, Mohammad Ghazaiean, Mobin Kosaryan, Mehrnoush Mosanejad-Galchali, Amir Aliasgharian, Aily Karami, Hasan |
description | Hypozincemia is a prevalent adverse consequence in diabetes mellitus (DM) and [beta]-Thalassemia patients. We aimed to evaluate the level of serum zinc in [beta]-thalassemia patients with DM and a risk assessment for hypozincemia. The study population included transfusion-dependent thalassemia (TDT) and non-transfusion-dependent thalassemia (NTDT) with overt DM (fasting plasma glucose (FPG) [greater than or equal to]126 mg/dL, and/or 2-h plasma glucose[greater than or equal to]200 mg/dL). Serum zinc concentration was measured by the colorimetric method, and the values below 70 [mu]g/dL were defined as hypozincemia. Myocardial and liver T2*-weighted magnetic resonance imaging (MRI T2*, millisecond [ms]) were valued by a free contrast MRI. The demographic, clinical, paraclinical, and laboratory data were also recorded. The data belonged to the period from December 2018 until December 2020. Of 64 diabetic [beta]-thalassemia patients, 41 cases had zinc data in their medical files (aged 38 ± 9 years, 48.8% female). 78.05% of patients (n = 32) were TDT, and 21.95% were NTDT (n = 9). The mean ± standard deviation of zinc level was 110.2 ± 127.6 [mu]g/dL. The prevalence of hypozincemia was 9.76%, 95% confidence interval [CI] 0.27 to 19.24 (four cases). After controlling age, the odds of hypozincemia for using deferasirox (DFX) was 8.77, 95% CI 0.60 to 127.1. In [beta]-thalassemia patients, the age-adjusted risk of hypozincemia was calculated at 15.85, 95% CI 0.47 to 529.3 for hepatitis C. The adjusted risk of hypozincemia based on age for antacid use was 6.34, 95% CI 0.39 to 102.7. In light of this study, as well as hepatitis C, using DFX and antacids is associated with a high risk of hypozincemia amid diabetic [beta]-thalassemia cases. However, upward bias should be taken into consideration. |
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We aimed to evaluate the level of serum zinc in [beta]-thalassemia patients with DM and a risk assessment for hypozincemia. The study population included transfusion-dependent thalassemia (TDT) and non-transfusion-dependent thalassemia (NTDT) with overt DM (fasting plasma glucose (FPG) [greater than or equal to]126 mg/dL, and/or 2-h plasma glucose[greater than or equal to]200 mg/dL). Serum zinc concentration was measured by the colorimetric method, and the values below 70 [mu]g/dL were defined as hypozincemia. Myocardial and liver T2*-weighted magnetic resonance imaging (MRI T2*, millisecond [ms]) were valued by a free contrast MRI. The demographic, clinical, paraclinical, and laboratory data were also recorded. The data belonged to the period from December 2018 until December 2020. Of 64 diabetic [beta]-thalassemia patients, 41 cases had zinc data in their medical files (aged 38 ± 9 years, 48.8% female). 78.05% of patients (n = 32) were TDT, and 21.95% were NTDT (n = 9). The mean ± standard deviation of zinc level was 110.2 ± 127.6 [mu]g/dL. The prevalence of hypozincemia was 9.76%, 95% confidence interval [CI] 0.27 to 19.24 (four cases). After controlling age, the odds of hypozincemia for using deferasirox (DFX) was 8.77, 95% CI 0.60 to 127.1. In [beta]-thalassemia patients, the age-adjusted risk of hypozincemia was calculated at 15.85, 95% CI 0.47 to 529.3 for hepatitis C. The adjusted risk of hypozincemia based on age for antacid use was 6.34, 95% CI 0.39 to 102.7. In light of this study, as well as hepatitis C, using DFX and antacids is associated with a high risk of hypozincemia amid diabetic [beta]-thalassemia cases. However, upward bias should be taken into consideration.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0284267</identifier><language>eng</language><publisher>Public Library of Science</publisher><subject>Antacids ; Development and progression ; Dextrose ; Diabetes ; Drug therapy ; Glucose ; Health aspects ; Hepatitis C ; Risk assessment ; Risk factors ; Thalassemia ; Zinc in the body</subject><ispartof>PloS one, 2024-01, Vol.19 (1), p.e0284267</ispartof><rights>COPYRIGHT 2024 Public Library of Science</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,860,27901,27902</link.rule.ids></links><search><creatorcontrib>Darvishi-Khezri, Hadi</creatorcontrib><creatorcontrib>Karami, Hossein</creatorcontrib><creatorcontrib>Naderisorki, Mohammad</creatorcontrib><creatorcontrib>Ghazaiean, Mobin</creatorcontrib><creatorcontrib>Kosaryan, Mehrnoush</creatorcontrib><creatorcontrib>Mosanejad-Galchali, Amir</creatorcontrib><creatorcontrib>Aliasgharian, Aily</creatorcontrib><creatorcontrib>Karami, Hasan</creatorcontrib><title>Two risk factors for hypozincemia in diabetic [beta]-thalassemia patients: Hepatitis C and deferasirox</title><title>PloS one</title><description>Hypozincemia is a prevalent adverse consequence in diabetes mellitus (DM) and [beta]-Thalassemia patients. We aimed to evaluate the level of serum zinc in [beta]-thalassemia patients with DM and a risk assessment for hypozincemia. The study population included transfusion-dependent thalassemia (TDT) and non-transfusion-dependent thalassemia (NTDT) with overt DM (fasting plasma glucose (FPG) [greater than or equal to]126 mg/dL, and/or 2-h plasma glucose[greater than or equal to]200 mg/dL). Serum zinc concentration was measured by the colorimetric method, and the values below 70 [mu]g/dL were defined as hypozincemia. Myocardial and liver T2*-weighted magnetic resonance imaging (MRI T2*, millisecond [ms]) were valued by a free contrast MRI. The demographic, clinical, paraclinical, and laboratory data were also recorded. The data belonged to the period from December 2018 until December 2020. Of 64 diabetic [beta]-thalassemia patients, 41 cases had zinc data in their medical files (aged 38 ± 9 years, 48.8% female). 78.05% of patients (n = 32) were TDT, and 21.95% were NTDT (n = 9). The mean ± standard deviation of zinc level was 110.2 ± 127.6 [mu]g/dL. The prevalence of hypozincemia was 9.76%, 95% confidence interval [CI] 0.27 to 19.24 (four cases). After controlling age, the odds of hypozincemia for using deferasirox (DFX) was 8.77, 95% CI 0.60 to 127.1. In [beta]-thalassemia patients, the age-adjusted risk of hypozincemia was calculated at 15.85, 95% CI 0.47 to 529.3 for hepatitis C. The adjusted risk of hypozincemia based on age for antacid use was 6.34, 95% CI 0.39 to 102.7. In light of this study, as well as hepatitis C, using DFX and antacids is associated with a high risk of hypozincemia amid diabetic [beta]-thalassemia cases. However, upward bias should be taken into consideration.</description><subject>Antacids</subject><subject>Development and progression</subject><subject>Dextrose</subject><subject>Diabetes</subject><subject>Drug therapy</subject><subject>Glucose</subject><subject>Health aspects</subject><subject>Hepatitis C</subject><subject>Risk assessment</subject><subject>Risk factors</subject><subject>Thalassemia</subject><subject>Zinc in the body</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqNkEFLAzEQhRdRsFb_gYeAIHjYNdnsJl1vpagtFApavYiU2U3STd0mZZNi9debqocWPMgc3jDzvYE3UXROcEIoJ9cLu24NNMnKGpngtJeljB9EHVLQNGYppoc7_XF04twC45z2GOtEavpuUavdG1JQeds6pGyL6o-V_dSmkksNSBskNJTS6wq9BIHX2NfQgHPf6xV4LY13N2got73XDg0QGIGEVLIFp1u7OY2OFDROnv1qN3q6u50OhvF4cj8a9MfxnDCWxpRlDHOcFSUpyjQrFc6ygrKc5QVmHAjDOaGSyFxSwUtW5qKUQgEXAVchIe1GFz9359DImTbK-haqpXbVrM95kWJS8C2V_EGFEiFRFZ6odJjvGa72DIHxcuPnsHZuNnp8-D87ed5nL3fYWkLja2ebtdfWuF3wC9p3k34</recordid><startdate>20240112</startdate><enddate>20240112</enddate><creator>Darvishi-Khezri, Hadi</creator><creator>Karami, Hossein</creator><creator>Naderisorki, Mohammad</creator><creator>Ghazaiean, Mobin</creator><creator>Kosaryan, Mehrnoush</creator><creator>Mosanejad-Galchali, Amir</creator><creator>Aliasgharian, Aily</creator><creator>Karami, Hasan</creator><general>Public Library of Science</general><scope>IOV</scope><scope>ISR</scope></search><sort><creationdate>20240112</creationdate><title>Two risk factors for hypozincemia in diabetic [beta]-thalassemia patients: Hepatitis C and deferasirox</title><author>Darvishi-Khezri, Hadi ; Karami, Hossein ; Naderisorki, Mohammad ; Ghazaiean, Mobin ; Kosaryan, Mehrnoush ; Mosanejad-Galchali, Amir ; Aliasgharian, Aily ; Karami, Hasan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-g1662-364607049b19b24bf0449365659067a160513e1e5e3d7b6b5dbedfa7d19bf9323</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Antacids</topic><topic>Development and progression</topic><topic>Dextrose</topic><topic>Diabetes</topic><topic>Drug therapy</topic><topic>Glucose</topic><topic>Health aspects</topic><topic>Hepatitis C</topic><topic>Risk assessment</topic><topic>Risk factors</topic><topic>Thalassemia</topic><topic>Zinc in the body</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Darvishi-Khezri, Hadi</creatorcontrib><creatorcontrib>Karami, Hossein</creatorcontrib><creatorcontrib>Naderisorki, Mohammad</creatorcontrib><creatorcontrib>Ghazaiean, Mobin</creatorcontrib><creatorcontrib>Kosaryan, Mehrnoush</creatorcontrib><creatorcontrib>Mosanejad-Galchali, Amir</creatorcontrib><creatorcontrib>Aliasgharian, Aily</creatorcontrib><creatorcontrib>Karami, Hasan</creatorcontrib><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Darvishi-Khezri, Hadi</au><au>Karami, Hossein</au><au>Naderisorki, Mohammad</au><au>Ghazaiean, Mobin</au><au>Kosaryan, Mehrnoush</au><au>Mosanejad-Galchali, Amir</au><au>Aliasgharian, Aily</au><au>Karami, Hasan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Two risk factors for hypozincemia in diabetic [beta]-thalassemia patients: Hepatitis C and deferasirox</atitle><jtitle>PloS one</jtitle><date>2024-01-12</date><risdate>2024</risdate><volume>19</volume><issue>1</issue><spage>e0284267</spage><pages>e0284267-</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Hypozincemia is a prevalent adverse consequence in diabetes mellitus (DM) and [beta]-Thalassemia patients. We aimed to evaluate the level of serum zinc in [beta]-thalassemia patients with DM and a risk assessment for hypozincemia. The study population included transfusion-dependent thalassemia (TDT) and non-transfusion-dependent thalassemia (NTDT) with overt DM (fasting plasma glucose (FPG) [greater than or equal to]126 mg/dL, and/or 2-h plasma glucose[greater than or equal to]200 mg/dL). Serum zinc concentration was measured by the colorimetric method, and the values below 70 [mu]g/dL were defined as hypozincemia. Myocardial and liver T2*-weighted magnetic resonance imaging (MRI T2*, millisecond [ms]) were valued by a free contrast MRI. The demographic, clinical, paraclinical, and laboratory data were also recorded. The data belonged to the period from December 2018 until December 2020. Of 64 diabetic [beta]-thalassemia patients, 41 cases had zinc data in their medical files (aged 38 ± 9 years, 48.8% female). 78.05% of patients (n = 32) were TDT, and 21.95% were NTDT (n = 9). The mean ± standard deviation of zinc level was 110.2 ± 127.6 [mu]g/dL. The prevalence of hypozincemia was 9.76%, 95% confidence interval [CI] 0.27 to 19.24 (four cases). After controlling age, the odds of hypozincemia for using deferasirox (DFX) was 8.77, 95% CI 0.60 to 127.1. In [beta]-thalassemia patients, the age-adjusted risk of hypozincemia was calculated at 15.85, 95% CI 0.47 to 529.3 for hepatitis C. The adjusted risk of hypozincemia based on age for antacid use was 6.34, 95% CI 0.39 to 102.7. In light of this study, as well as hepatitis C, using DFX and antacids is associated with a high risk of hypozincemia amid diabetic [beta]-thalassemia cases. However, upward bias should be taken into consideration.</abstract><pub>Public Library of Science</pub><doi>10.1371/journal.pone.0284267</doi><tpages>e0284267</tpages></addata></record> |
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subjects | Antacids Development and progression Dextrose Diabetes Drug therapy Glucose Health aspects Hepatitis C Risk assessment Risk factors Thalassemia Zinc in the body |
title | Two risk factors for hypozincemia in diabetic [beta]-thalassemia patients: Hepatitis C and deferasirox |
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