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The effect of different types of anemia on HbA1c levels in non-diabetics
Diabetes mellitus is one of the most common diseases worldwide with significant morbidity and mortality. HbA1c remains one of the most important methods for diagnosis and monitoring of the disease. Since HbA1c is a reflection of the glucose attached to red blood cells, factors affecting hemoglobin a...
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Published in: | BMC endocrine disorders 2023-01, Vol.23 (1), p.24-24, Article 24 |
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description | Diabetes mellitus is one of the most common diseases worldwide with significant morbidity and mortality. HbA1c remains one of the most important methods for diagnosis and monitoring of the disease. Since HbA1c is a reflection of the glucose attached to red blood cells, factors affecting hemoglobin and red blood cells' half-life can influence HbA1c measurements.
This study aims to evaluate the effect of different types of anemia including iron deficiency anemia, sickle cell anemia, β -thalassemia trait, and megaloblastic anemia on HbA1c levels in a tertiary hospital over the past 6 years (2016-2022).
This is a retrospective chart review study of 324 patients including those with one of the four types of anemia mentioned above and a control group. The control group were healthy adults with normal HbA1c and hemoglobin, who were not known to have diabetes or anemia. Patients with diabetes or prediabetes based on self-reporting or elevated fasting, random blood sugar, or 2 hours post-prandial blood glucose were excluded.
The mean HbA1c levels were significantly higher in sickle cell anemia at 5.83% (95% CI = 5.39-6.28) and in iron deficiency anemia at 5.75% (95% CI = 5.68-5.82) when compared to the control group at 5.32% (95% CI = 5.22-5.41). However, the mean HbA1c levels in megaloblastic anemia were 5.38% (95% CI = 5.26-5.5) and 5.45% (95% CI = 5.21-5.69) in beta thalassemia trait, which were not significantly different when compared to the control group. HbA1c significantly decreased from 5.75 to 5.44% after treatment in the iron-deficient group with a p-value of |
doi_str_mv | 10.1186/s12902-023-01280-y |
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This study aims to evaluate the effect of different types of anemia including iron deficiency anemia, sickle cell anemia, β -thalassemia trait, and megaloblastic anemia on HbA1c levels in a tertiary hospital over the past 6 years (2016-2022).
This is a retrospective chart review study of 324 patients including those with one of the four types of anemia mentioned above and a control group. The control group were healthy adults with normal HbA1c and hemoglobin, who were not known to have diabetes or anemia. Patients with diabetes or prediabetes based on self-reporting or elevated fasting, random blood sugar, or 2 hours post-prandial blood glucose were excluded.
The mean HbA1c levels were significantly higher in sickle cell anemia at 5.83% (95% CI = 5.39-6.28) and in iron deficiency anemia at 5.75% (95% CI = 5.68-5.82) when compared to the control group at 5.32% (95% CI = 5.22-5.41). However, the mean HbA1c levels in megaloblastic anemia were 5.38% (95% CI = 5.26-5.5) and 5.45% (95% CI = 5.21-5.69) in beta thalassemia trait, which were not significantly different when compared to the control group. HbA1c significantly decreased from 5.75 to 5.44% after treatment in the iron-deficient group with a p-value of < 0.001. Moreover, lower hemoglobin and higher red cell distribution width correlated with higher HbA1c levels in patients with sickle cell anemia.
This study found a significant increase in HbA1c levels in iron deficiency anemia and sickle cell disease in patients not known to have diabetes. However, there was no significant effect in those patients with β-thalassemia trait and megaloblastic anemia. Treatment of iron deficiency anemia significantly decreased the HbA1c level, bringing it back to normal.</description><identifier>ISSN: 1472-6823</identifier><identifier>EISSN: 1472-6823</identifier><identifier>DOI: 10.1186/s12902-023-01280-y</identifier><identifier>PMID: 36709277</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Adult ; Anemia ; Anemia, Iron-Deficiency - diagnosis ; Anemia, Megaloblastic ; Anemia, Sickle Cell ; beta-Thalassemia - complications ; beta-Thalassemia - diagnosis ; Blood diseases ; Blood sugar ; Data collection ; Diabetes ; Diabetes mellitus ; Diabetes Mellitus - diagnosis ; Diabetics ; Electronic health records ; Erythrocytes ; Glucose ; Glycated Hemoglobin ; Glycosylated hemoglobin ; HbA1c ; Health aspects ; Health care ; Hemoglobin ; Hemoglobins ; Humans ; Iron ; Iron deficiency ; Iron deficiency anemia ; Medical records ; Medical research ; Medicine, Experimental ; Megaloblastic anemia ; Morbidity ; Mortality ; Nutrient deficiency ; Patients ; Prediabetic state ; Retrospective Studies ; Sickle cell anemia ; Sickle cell disease ; Thalassemia ; Womens health ; β-Thalassemia trait</subject><ispartof>BMC endocrine disorders, 2023-01, Vol.23 (1), p.24-24, Article 24</ispartof><rights>2023. The Author(s).</rights><rights>COPYRIGHT 2023 BioMed Central Ltd.</rights><rights>2023. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c563t-91eaf8bca65befcdcdbb232bf71e309502d6b0bde7e14df9f5b0f91857fb54bc3</citedby><cites>FETCH-LOGICAL-c563t-91eaf8bca65befcdcdbb232bf71e309502d6b0bde7e14df9f5b0f91857fb54bc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9883954/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2777771485?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36709277$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Alzahrani, Basil A</creatorcontrib><creatorcontrib>Salamatullah, Hassan K</creatorcontrib><creatorcontrib>Alsharm, Faisal S</creatorcontrib><creatorcontrib>Baljoon, Jamil M</creatorcontrib><creatorcontrib>Abukhodair, Abdullah O</creatorcontrib><creatorcontrib>Ahmed, Mohammed Eldigire</creatorcontrib><creatorcontrib>Malaikah, Hebah</creatorcontrib><creatorcontrib>Radi, Suhaib</creatorcontrib><title>The effect of different types of anemia on HbA1c levels in non-diabetics</title><title>BMC endocrine disorders</title><addtitle>BMC Endocr Disord</addtitle><description>Diabetes mellitus is one of the most common diseases worldwide with significant morbidity and mortality. HbA1c remains one of the most important methods for diagnosis and monitoring of the disease. Since HbA1c is a reflection of the glucose attached to red blood cells, factors affecting hemoglobin and red blood cells' half-life can influence HbA1c measurements.
This study aims to evaluate the effect of different types of anemia including iron deficiency anemia, sickle cell anemia, β -thalassemia trait, and megaloblastic anemia on HbA1c levels in a tertiary hospital over the past 6 years (2016-2022).
This is a retrospective chart review study of 324 patients including those with one of the four types of anemia mentioned above and a control group. The control group were healthy adults with normal HbA1c and hemoglobin, who were not known to have diabetes or anemia. Patients with diabetes or prediabetes based on self-reporting or elevated fasting, random blood sugar, or 2 hours post-prandial blood glucose were excluded.
The mean HbA1c levels were significantly higher in sickle cell anemia at 5.83% (95% CI = 5.39-6.28) and in iron deficiency anemia at 5.75% (95% CI = 5.68-5.82) when compared to the control group at 5.32% (95% CI = 5.22-5.41). However, the mean HbA1c levels in megaloblastic anemia were 5.38% (95% CI = 5.26-5.5) and 5.45% (95% CI = 5.21-5.69) in beta thalassemia trait, which were not significantly different when compared to the control group. HbA1c significantly decreased from 5.75 to 5.44% after treatment in the iron-deficient group with a p-value of < 0.001. Moreover, lower hemoglobin and higher red cell distribution width correlated with higher HbA1c levels in patients with sickle cell anemia.
This study found a significant increase in HbA1c levels in iron deficiency anemia and sickle cell disease in patients not known to have diabetes. However, there was no significant effect in those patients with β-thalassemia trait and megaloblastic anemia. Treatment of iron deficiency anemia significantly decreased the HbA1c level, bringing it back to normal.</description><subject>Adult</subject><subject>Anemia</subject><subject>Anemia, Iron-Deficiency - diagnosis</subject><subject>Anemia, Megaloblastic</subject><subject>Anemia, Sickle Cell</subject><subject>beta-Thalassemia - complications</subject><subject>beta-Thalassemia - diagnosis</subject><subject>Blood diseases</subject><subject>Blood sugar</subject><subject>Data collection</subject><subject>Diabetes</subject><subject>Diabetes mellitus</subject><subject>Diabetes Mellitus - diagnosis</subject><subject>Diabetics</subject><subject>Electronic health records</subject><subject>Erythrocytes</subject><subject>Glucose</subject><subject>Glycated Hemoglobin</subject><subject>Glycosylated hemoglobin</subject><subject>HbA1c</subject><subject>Health aspects</subject><subject>Health care</subject><subject>Hemoglobin</subject><subject>Hemoglobins</subject><subject>Humans</subject><subject>Iron</subject><subject>Iron deficiency</subject><subject>Iron deficiency anemia</subject><subject>Medical records</subject><subject>Medical research</subject><subject>Medicine, Experimental</subject><subject>Megaloblastic anemia</subject><subject>Morbidity</subject><subject>Mortality</subject><subject>Nutrient deficiency</subject><subject>Patients</subject><subject>Prediabetic state</subject><subject>Retrospective Studies</subject><subject>Sickle cell anemia</subject><subject>Sickle cell disease</subject><subject>Thalassemia</subject><subject>Womens health</subject><subject>β-Thalassemia trait</subject><issn>1472-6823</issn><issn>1472-6823</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptUk1vEzEQtRCIlsAf4IBW4sJliz_X9gWpqoBUqsSlnC1_jFNHGzusN5Xy73GaUhqELcuj8XvPnvFD6D3BF4So4XMlVGPaY8p6TKjC_f4FOidc0n5QlL18Fp-hN7WuMSZSUfwanbFBYk2lPEfL2zvoIEbwc1diF1ILJ8hzN--3UA8pm2GTbFdyt3SXxHcj3MNYu5S7XHIfknUwJ1_folfRjhXePe4L9PPb19urZX_z4_v11eVN78XA5l4TsFE5bwfhIPrgg3OUURclAYa1wDQMDrsAEggPUUfhcNRECRmd4M6zBbo-6oZi12Y7pY2d9qbYZB4SZVoZO7UHjWAos1RwLQYrFA8U28iZp5Jr4MNgrW5aX45a253bQPCt7smOJ6KnJzndmVW5N1oppgVvAp8eBabyawd1NptUPYxja1rZVdNajLlUjKsG_fgPdF12U26tOqDaIFyJv6iVbQWkHEu71x9EzaVkAg9MtbVAF_9BtRnaV_mSIaaWPyHQI8FPpdYJ4lONBJuDl8zRS6Z5yTx4yewb6cPz7jxR_piH_QarUsMv</recordid><startdate>20230128</startdate><enddate>20230128</enddate><creator>Alzahrani, Basil A</creator><creator>Salamatullah, Hassan K</creator><creator>Alsharm, Faisal S</creator><creator>Baljoon, Jamil M</creator><creator>Abukhodair, Abdullah O</creator><creator>Ahmed, Mohammed Eldigire</creator><creator>Malaikah, Hebah</creator><creator>Radi, Suhaib</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20230128</creationdate><title>The effect of different types of anemia on HbA1c levels in non-diabetics</title><author>Alzahrani, Basil A ; Salamatullah, Hassan K ; Alsharm, Faisal S ; Baljoon, Jamil M ; Abukhodair, Abdullah O ; Ahmed, Mohammed Eldigire ; Malaikah, Hebah ; Radi, Suhaib</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c563t-91eaf8bca65befcdcdbb232bf71e309502d6b0bde7e14df9f5b0f91857fb54bc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Adult</topic><topic>Anemia</topic><topic>Anemia, Iron-Deficiency - diagnosis</topic><topic>Anemia, Megaloblastic</topic><topic>Anemia, Sickle Cell</topic><topic>beta-Thalassemia - complications</topic><topic>beta-Thalassemia - diagnosis</topic><topic>Blood diseases</topic><topic>Blood sugar</topic><topic>Data collection</topic><topic>Diabetes</topic><topic>Diabetes mellitus</topic><topic>Diabetes Mellitus - diagnosis</topic><topic>Diabetics</topic><topic>Electronic health records</topic><topic>Erythrocytes</topic><topic>Glucose</topic><topic>Glycated Hemoglobin</topic><topic>Glycosylated hemoglobin</topic><topic>HbA1c</topic><topic>Health aspects</topic><topic>Health care</topic><topic>Hemoglobin</topic><topic>Hemoglobins</topic><topic>Humans</topic><topic>Iron</topic><topic>Iron deficiency</topic><topic>Iron deficiency anemia</topic><topic>Medical records</topic><topic>Medical research</topic><topic>Medicine, Experimental</topic><topic>Megaloblastic anemia</topic><topic>Morbidity</topic><topic>Mortality</topic><topic>Nutrient deficiency</topic><topic>Patients</topic><topic>Prediabetic state</topic><topic>Retrospective Studies</topic><topic>Sickle cell anemia</topic><topic>Sickle cell disease</topic><topic>Thalassemia</topic><topic>Womens health</topic><topic>β-Thalassemia trait</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Alzahrani, Basil A</creatorcontrib><creatorcontrib>Salamatullah, Hassan K</creatorcontrib><creatorcontrib>Alsharm, Faisal S</creatorcontrib><creatorcontrib>Baljoon, Jamil M</creatorcontrib><creatorcontrib>Abukhodair, Abdullah O</creatorcontrib><creatorcontrib>Ahmed, Mohammed Eldigire</creatorcontrib><creatorcontrib>Malaikah, Hebah</creatorcontrib><creatorcontrib>Radi, Suhaib</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>BMC endocrine disorders</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Alzahrani, Basil A</au><au>Salamatullah, Hassan K</au><au>Alsharm, Faisal S</au><au>Baljoon, Jamil M</au><au>Abukhodair, Abdullah O</au><au>Ahmed, Mohammed Eldigire</au><au>Malaikah, Hebah</au><au>Radi, Suhaib</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The effect of different types of anemia on HbA1c levels in non-diabetics</atitle><jtitle>BMC endocrine disorders</jtitle><addtitle>BMC Endocr Disord</addtitle><date>2023-01-28</date><risdate>2023</risdate><volume>23</volume><issue>1</issue><spage>24</spage><epage>24</epage><pages>24-24</pages><artnum>24</artnum><issn>1472-6823</issn><eissn>1472-6823</eissn><abstract>Diabetes mellitus is one of the most common diseases worldwide with significant morbidity and mortality. HbA1c remains one of the most important methods for diagnosis and monitoring of the disease. Since HbA1c is a reflection of the glucose attached to red blood cells, factors affecting hemoglobin and red blood cells' half-life can influence HbA1c measurements.
This study aims to evaluate the effect of different types of anemia including iron deficiency anemia, sickle cell anemia, β -thalassemia trait, and megaloblastic anemia on HbA1c levels in a tertiary hospital over the past 6 years (2016-2022).
This is a retrospective chart review study of 324 patients including those with one of the four types of anemia mentioned above and a control group. The control group were healthy adults with normal HbA1c and hemoglobin, who were not known to have diabetes or anemia. Patients with diabetes or prediabetes based on self-reporting or elevated fasting, random blood sugar, or 2 hours post-prandial blood glucose were excluded.
The mean HbA1c levels were significantly higher in sickle cell anemia at 5.83% (95% CI = 5.39-6.28) and in iron deficiency anemia at 5.75% (95% CI = 5.68-5.82) when compared to the control group at 5.32% (95% CI = 5.22-5.41). However, the mean HbA1c levels in megaloblastic anemia were 5.38% (95% CI = 5.26-5.5) and 5.45% (95% CI = 5.21-5.69) in beta thalassemia trait, which were not significantly different when compared to the control group. HbA1c significantly decreased from 5.75 to 5.44% after treatment in the iron-deficient group with a p-value of < 0.001. Moreover, lower hemoglobin and higher red cell distribution width correlated with higher HbA1c levels in patients with sickle cell anemia.
This study found a significant increase in HbA1c levels in iron deficiency anemia and sickle cell disease in patients not known to have diabetes. However, there was no significant effect in those patients with β-thalassemia trait and megaloblastic anemia. Treatment of iron deficiency anemia significantly decreased the HbA1c level, bringing it back to normal.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>36709277</pmid><doi>10.1186/s12902-023-01280-y</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Anemia Anemia, Iron-Deficiency - diagnosis Anemia, Megaloblastic Anemia, Sickle Cell beta-Thalassemia - complications beta-Thalassemia - diagnosis Blood diseases Blood sugar Data collection Diabetes Diabetes mellitus Diabetes Mellitus - diagnosis Diabetics Electronic health records Erythrocytes Glucose Glycated Hemoglobin Glycosylated hemoglobin HbA1c Health aspects Health care Hemoglobin Hemoglobins Humans Iron Iron deficiency Iron deficiency anemia Medical records Medical research Medicine, Experimental Megaloblastic anemia Morbidity Mortality Nutrient deficiency Patients Prediabetic state Retrospective Studies Sickle cell anemia Sickle cell disease Thalassemia Womens health β-Thalassemia trait |
title | The effect of different types of anemia on HbA1c levels in non-diabetics |
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