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Relationship between hyperglycemia, antioxidant capacity and some enzymatic and non-enzymatic antioxidants in African patients with type 2 diabetes
Studies demonstrate that free radicals are involved in the pathogenesis of diabetic complications. The aim of this study was to determine the implication of total antioxidant capacity (TAC) and some enzymatic and non-enzymatic antioxidants as suitable biomarkers of diabetic complications risk factor...
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Published in: | BMC research notes 2017-03, Vol.10 (1), p.141-141, Article 141 |
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creator | Pieme, Constant Anatole Tatangmo, Jérôme Antony Simo, Gustave Biapa Nya, Prosper Cabral Ama Moor, Vicky Jocelyne Moukette Moukette, Bruno Tankeu Nzufo, Francine Njinkio Nono, Borgia Legrand Sobngwi, Eugene |
description | Studies demonstrate that free radicals are involved in the pathogenesis of diabetic complications. The aim of this study was to determine the implication of total antioxidant capacity (TAC) and some enzymatic and non-enzymatic antioxidants as suitable biomarkers of diabetic complications risk factors.
A total of 90 patients (70 patients with or without diabetic complications +20 normal healthy) were examined by evaluating the level of lipid peroxidation, nitrogen monoxide (NO), fasting blood glucose, glycated haemoglobin (HbA1c), enzymatic and non-enzymatic antioxidants using standard spectrophotometric methods.
The fasting blood glucose and HbA1c levels were respectively 2.05 and 2.32 times higher in the group of patients with diabetes and complications (DPWC) compared to those of healthy persons. A statistically higher level of malondialdehyde (MDA), NO and TAC was observed in a group of patients with diabetes and complications compared to those without complications (DPNC). A significant positive correlation was found between catalase (CAT) and fasting blood glucose while a significant and negative correlation was noted between reduced glutathione (GSH) and fasting blood glucose. Also was noted a significant relationship between HbA1c and other markers of oxidative stress.
The results suggest that the plasma levels of CAT, TAC and reduced glutathione could give information on the risk of developing complications of diabetes, considering that the modification of these biomarkers levels were associated with oxidative stress. |
doi_str_mv | 10.1186/s13104-017-2463-6 |
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A total of 90 patients (70 patients with or without diabetic complications +20 normal healthy) were examined by evaluating the level of lipid peroxidation, nitrogen monoxide (NO), fasting blood glucose, glycated haemoglobin (HbA1c), enzymatic and non-enzymatic antioxidants using standard spectrophotometric methods.
The fasting blood glucose and HbA1c levels were respectively 2.05 and 2.32 times higher in the group of patients with diabetes and complications (DPWC) compared to those of healthy persons. A statistically higher level of malondialdehyde (MDA), NO and TAC was observed in a group of patients with diabetes and complications compared to those without complications (DPNC). A significant positive correlation was found between catalase (CAT) and fasting blood glucose while a significant and negative correlation was noted between reduced glutathione (GSH) and fasting blood glucose. Also was noted a significant relationship between HbA1c and other markers of oxidative stress.
The results suggest that the plasma levels of CAT, TAC and reduced glutathione could give information on the risk of developing complications of diabetes, considering that the modification of these biomarkers levels were associated with oxidative stress.</description><identifier>ISSN: 1756-0500</identifier><identifier>EISSN: 1756-0500</identifier><identifier>DOI: 10.1186/s13104-017-2463-6</identifier><identifier>PMID: 28356165</identifier><language>eng</language><publisher>England: BioMed Central</publisher><subject>Adult ; Aged ; Antioxidants ; Antioxidants - metabolism ; Autoimmune diseases ; Biomarkers ; Biomarkers - blood ; Blood Glucose - metabolism ; Cameroon ; Catalase - blood ; Diabetes ; Diabetes mellitus ; Diabetes Mellitus, Type 2 - blood ; Diabetes Mellitus, Type 2 - complications ; Family medical history ; Fasting - blood ; Female ; Free radicals ; Glucose ; Glutathione - blood ; Glycated Hemoglobin - metabolism ; Hemoglobin ; Humans ; Hyperglycemia ; Hyperglycemia - blood ; Hyperglycemia - complications ; Hypertension ; Immunology ; Lipid Peroxidation ; Lipids ; Male ; Malondialdehyde ; Malondialdehyde - blood ; Metabolic disorders ; Methods ; Middle Aged ; Nitric Oxide - blood ; Oxidative Stress ; Pathogenesis ; Studies ; Superoxide Dismutase - blood ; Total Antioxidant Capacity ; Type 2 diabetes ; Vitamins</subject><ispartof>BMC research notes, 2017-03, Vol.10 (1), p.141-141, Article 141</ispartof><rights>Copyright BioMed Central 2017</rights><rights>The Author(s) 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4086-9ee3cb9289c7db6ed2f1de0a224005bd48241ccd8e5c2d5c8ab60d38298c00373</citedby><cites>FETCH-LOGICAL-c4086-9ee3cb9289c7db6ed2f1de0a224005bd48241ccd8e5c2d5c8ab60d38298c00373</cites><orcidid>0000-0003-1602-6494</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5372257/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1883238774?pq-origsite=primo$$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/28356165$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pieme, Constant Anatole</creatorcontrib><creatorcontrib>Tatangmo, Jérôme Antony</creatorcontrib><creatorcontrib>Simo, Gustave</creatorcontrib><creatorcontrib>Biapa Nya, Prosper Cabral</creatorcontrib><creatorcontrib>Ama Moor, Vicky Jocelyne</creatorcontrib><creatorcontrib>Moukette Moukette, Bruno</creatorcontrib><creatorcontrib>Tankeu Nzufo, Francine</creatorcontrib><creatorcontrib>Njinkio Nono, Borgia Legrand</creatorcontrib><creatorcontrib>Sobngwi, Eugene</creatorcontrib><title>Relationship between hyperglycemia, antioxidant capacity and some enzymatic and non-enzymatic antioxidants in African patients with type 2 diabetes</title><title>BMC research notes</title><addtitle>BMC Res Notes</addtitle><description>Studies demonstrate that free radicals are involved in the pathogenesis of diabetic complications. The aim of this study was to determine the implication of total antioxidant capacity (TAC) and some enzymatic and non-enzymatic antioxidants as suitable biomarkers of diabetic complications risk factors.
A total of 90 patients (70 patients with or without diabetic complications +20 normal healthy) were examined by evaluating the level of lipid peroxidation, nitrogen monoxide (NO), fasting blood glucose, glycated haemoglobin (HbA1c), enzymatic and non-enzymatic antioxidants using standard spectrophotometric methods.
The fasting blood glucose and HbA1c levels were respectively 2.05 and 2.32 times higher in the group of patients with diabetes and complications (DPWC) compared to those of healthy persons. A statistically higher level of malondialdehyde (MDA), NO and TAC was observed in a group of patients with diabetes and complications compared to those without complications (DPNC). A significant positive correlation was found between catalase (CAT) and fasting blood glucose while a significant and negative correlation was noted between reduced glutathione (GSH) and fasting blood glucose. Also was noted a significant relationship between HbA1c and other markers of oxidative stress.
The results suggest that the plasma levels of CAT, TAC and reduced glutathione could give information on the risk of developing complications of diabetes, considering that the modification of these biomarkers levels were associated with oxidative stress.</description><subject>Adult</subject><subject>Aged</subject><subject>Antioxidants</subject><subject>Antioxidants - metabolism</subject><subject>Autoimmune diseases</subject><subject>Biomarkers</subject><subject>Biomarkers - blood</subject><subject>Blood Glucose - metabolism</subject><subject>Cameroon</subject><subject>Catalase - blood</subject><subject>Diabetes</subject><subject>Diabetes mellitus</subject><subject>Diabetes Mellitus, Type 2 - blood</subject><subject>Diabetes Mellitus, Type 2 - complications</subject><subject>Family medical history</subject><subject>Fasting - blood</subject><subject>Female</subject><subject>Free radicals</subject><subject>Glucose</subject><subject>Glutathione - blood</subject><subject>Glycated Hemoglobin - metabolism</subject><subject>Hemoglobin</subject><subject>Humans</subject><subject>Hyperglycemia</subject><subject>Hyperglycemia - blood</subject><subject>Hyperglycemia - complications</subject><subject>Hypertension</subject><subject>Immunology</subject><subject>Lipid Peroxidation</subject><subject>Lipids</subject><subject>Male</subject><subject>Malondialdehyde</subject><subject>Malondialdehyde - blood</subject><subject>Metabolic disorders</subject><subject>Methods</subject><subject>Middle Aged</subject><subject>Nitric Oxide - blood</subject><subject>Oxidative Stress</subject><subject>Pathogenesis</subject><subject>Studies</subject><subject>Superoxide Dismutase - blood</subject><subject>Total Antioxidant Capacity</subject><subject>Type 2 diabetes</subject><subject>Vitamins</subject><issn>1756-0500</issn><issn>1756-0500</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdUk1v1DAQjRCIlsIP4IIsceFAwN9xLkhVVaBSJSQEZ8uxJ7teJXawsy3bv8EfxumW1Rb5MNabN29m7FdVrwn-QIiSHzNhBPMak6amXLJaPqlOSSNkjQXGT4_uJ9WLnDcYS6IUeV6dUMWEJFKcVn--w2BmH0Ne-wl1MN8CBLTeTZBWw87C6M17ZEJh_PauRGTNZKyfdwV0KMcREIS73Vg07D0UYqiPkUNlRj6g8z55awKaShYW7NbPazSXdogi500ZAPLL6llvhgyvHuJZ9fPz5Y-Lr_X1ty9XF-fXteVYyboFYLZrqWpt4zoJjvbEATaUcoxF57iinFjrFAhLnbDKdBI7pmirLMasYWfV1V7XRbPRU_KjSTsdjdf3QEwrbVLZYgBNqOKW8sZR6HgPzgjjVAfccWB9y1XR-rTXmrbdCM6W5ZIZHok-zgS_1qt4owVrKBXLMO8eBFL8tYU869FnC8NgAsRt1uXnqMCknEJ9-x91E7cplKdaWIwy1TS8sMieZVPMOUF_GIZgvdhH7-2ji330Yh8tS82b4y0OFf_8wv4CCc3EoQ</recordid><startdate>20170329</startdate><enddate>20170329</enddate><creator>Pieme, Constant Anatole</creator><creator>Tatangmo, Jérôme Antony</creator><creator>Simo, Gustave</creator><creator>Biapa Nya, Prosper Cabral</creator><creator>Ama Moor, Vicky Jocelyne</creator><creator>Moukette Moukette, Bruno</creator><creator>Tankeu Nzufo, Francine</creator><creator>Njinkio Nono, Borgia Legrand</creator><creator>Sobngwi, Eugene</creator><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>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</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><orcidid>https://orcid.org/0000-0003-1602-6494</orcidid></search><sort><creationdate>20170329</creationdate><title>Relationship between hyperglycemia, antioxidant capacity and some enzymatic and non-enzymatic antioxidants in African patients with type 2 diabetes</title><author>Pieme, Constant Anatole ; Tatangmo, Jérôme Antony ; Simo, Gustave ; Biapa Nya, Prosper Cabral ; Ama Moor, Vicky Jocelyne ; Moukette Moukette, Bruno ; Tankeu Nzufo, Francine ; Njinkio Nono, Borgia Legrand ; Sobngwi, Eugene</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4086-9ee3cb9289c7db6ed2f1de0a224005bd48241ccd8e5c2d5c8ab60d38298c00373</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Antioxidants</topic><topic>Antioxidants - metabolism</topic><topic>Autoimmune diseases</topic><topic>Biomarkers</topic><topic>Biomarkers - blood</topic><topic>Blood Glucose - metabolism</topic><topic>Cameroon</topic><topic>Catalase - blood</topic><topic>Diabetes</topic><topic>Diabetes mellitus</topic><topic>Diabetes Mellitus, Type 2 - blood</topic><topic>Diabetes Mellitus, Type 2 - complications</topic><topic>Family medical history</topic><topic>Fasting - blood</topic><topic>Female</topic><topic>Free radicals</topic><topic>Glucose</topic><topic>Glutathione - blood</topic><topic>Glycated Hemoglobin - metabolism</topic><topic>Hemoglobin</topic><topic>Humans</topic><topic>Hyperglycemia</topic><topic>Hyperglycemia - blood</topic><topic>Hyperglycemia - complications</topic><topic>Hypertension</topic><topic>Immunology</topic><topic>Lipid Peroxidation</topic><topic>Lipids</topic><topic>Male</topic><topic>Malondialdehyde</topic><topic>Malondialdehyde - blood</topic><topic>Metabolic disorders</topic><topic>Methods</topic><topic>Middle Aged</topic><topic>Nitric Oxide - blood</topic><topic>Oxidative Stress</topic><topic>Pathogenesis</topic><topic>Studies</topic><topic>Superoxide Dismutase - blood</topic><topic>Total Antioxidant Capacity</topic><topic>Type 2 diabetes</topic><topic>Vitamins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pieme, Constant Anatole</creatorcontrib><creatorcontrib>Tatangmo, Jérôme Antony</creatorcontrib><creatorcontrib>Simo, Gustave</creatorcontrib><creatorcontrib>Biapa Nya, Prosper Cabral</creatorcontrib><creatorcontrib>Ama Moor, Vicky Jocelyne</creatorcontrib><creatorcontrib>Moukette Moukette, Bruno</creatorcontrib><creatorcontrib>Tankeu Nzufo, Francine</creatorcontrib><creatorcontrib>Njinkio Nono, Borgia Legrand</creatorcontrib><creatorcontrib>Sobngwi, Eugene</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>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</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>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Natural Science Collection</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 Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science 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 research notes</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pieme, Constant Anatole</au><au>Tatangmo, Jérôme Antony</au><au>Simo, Gustave</au><au>Biapa Nya, Prosper Cabral</au><au>Ama Moor, Vicky Jocelyne</au><au>Moukette Moukette, Bruno</au><au>Tankeu Nzufo, Francine</au><au>Njinkio Nono, Borgia Legrand</au><au>Sobngwi, Eugene</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Relationship between hyperglycemia, antioxidant capacity and some enzymatic and non-enzymatic antioxidants in African patients with type 2 diabetes</atitle><jtitle>BMC research notes</jtitle><addtitle>BMC Res Notes</addtitle><date>2017-03-29</date><risdate>2017</risdate><volume>10</volume><issue>1</issue><spage>141</spage><epage>141</epage><pages>141-141</pages><artnum>141</artnum><issn>1756-0500</issn><eissn>1756-0500</eissn><abstract>Studies demonstrate that free radicals are involved in the pathogenesis of diabetic complications. The aim of this study was to determine the implication of total antioxidant capacity (TAC) and some enzymatic and non-enzymatic antioxidants as suitable biomarkers of diabetic complications risk factors.
A total of 90 patients (70 patients with or without diabetic complications +20 normal healthy) were examined by evaluating the level of lipid peroxidation, nitrogen monoxide (NO), fasting blood glucose, glycated haemoglobin (HbA1c), enzymatic and non-enzymatic antioxidants using standard spectrophotometric methods.
The fasting blood glucose and HbA1c levels were respectively 2.05 and 2.32 times higher in the group of patients with diabetes and complications (DPWC) compared to those of healthy persons. A statistically higher level of malondialdehyde (MDA), NO and TAC was observed in a group of patients with diabetes and complications compared to those without complications (DPNC). A significant positive correlation was found between catalase (CAT) and fasting blood glucose while a significant and negative correlation was noted between reduced glutathione (GSH) and fasting blood glucose. Also was noted a significant relationship between HbA1c and other markers of oxidative stress.
The results suggest that the plasma levels of CAT, TAC and reduced glutathione could give information on the risk of developing complications of diabetes, considering that the modification of these biomarkers levels were associated with oxidative stress.</abstract><cop>England</cop><pub>BioMed Central</pub><pmid>28356165</pmid><doi>10.1186/s13104-017-2463-6</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0003-1602-6494</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Antioxidants Antioxidants - metabolism Autoimmune diseases Biomarkers Biomarkers - blood Blood Glucose - metabolism Cameroon Catalase - blood Diabetes Diabetes mellitus Diabetes Mellitus, Type 2 - blood Diabetes Mellitus, Type 2 - complications Family medical history Fasting - blood Female Free radicals Glucose Glutathione - blood Glycated Hemoglobin - metabolism Hemoglobin Humans Hyperglycemia Hyperglycemia - blood Hyperglycemia - complications Hypertension Immunology Lipid Peroxidation Lipids Male Malondialdehyde Malondialdehyde - blood Metabolic disorders Methods Middle Aged Nitric Oxide - blood Oxidative Stress Pathogenesis Studies Superoxide Dismutase - blood Total Antioxidant Capacity Type 2 diabetes Vitamins |
title | Relationship between hyperglycemia, antioxidant capacity and some enzymatic and non-enzymatic antioxidants in African patients with type 2 diabetes |
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