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Using plasma acute-phase protein concentrations to interpret nutritional biomarkers in apparently healthy HIV-1-seropositive Kenyan adults
Inflammation influences the assessment of nutritional status. For example, inflammation reduces plasma retinol concentrations and vitamin A deficiency is overestimated. Conversely inflammation increases plasma ferritin concentrations and Fe deficiency is underestimated. Blood samples were obtained f...
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Published in: | British journal of nutrition 2008-07, Vol.100 (1), p.174-182 |
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description | Inflammation influences the assessment of nutritional status. For example, inflammation reduces plasma retinol concentrations and vitamin A deficiency is overestimated. Conversely inflammation increases plasma ferritin concentrations and Fe deficiency is underestimated. Blood samples were obtained from 163 free-living HIV-1-infected adults, not on continuous medication, anti-retroviral drugs or micronutrients, not unwell and who had not reached WHO stage IV of HIV/AIDS. We used four markers of inflammation, C-reactive protein (CRP), α1-acid glycoprotein (AGP), α1-antichymotrypsin and erythrocyte sedimentation rate but mainly CRP and AGP were used to separate the subjects into four groups: ‘healthy’ where both CRP and AGP were normal; ‘incubation phase’ where CRP was elevated; ‘early convalescence’ where AGP and CRP were elevated and ‘late convalescence’ where only AGP was elevated. Correction factors were calculated to remove the influence of inflammation from each biomarker and group where inflammation was present and the data are shown before and after recalculation. The correction increased median plasma retinol concentrations of the whole group from 1·16 to 1·33 μmol/l, comparable with values (mean 1·29 μmol/l) in HIV-negative Kenyan women. Median ferritin concentrations fell by about 50 % in both sexes and the number of women with plasma ferritin concentrations ≤ 12 μg/l increased from eleven to twenty. The correction also increased plasma carotenoids and Hb but not α-tocopherol concentrations. We suggest that the method described to remove the influence of inflammation from nutritional biomarkers should be generally applicable in apparently healthy people and prevents discarding valuable data because of mild inflammation. The method does now need to be tested in other populations. |
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W. ; Mwaniki, David L. ; Muniu, Erastus M. ; Alumasa, Fred ; de Wagt, Arjan</creator><creatorcontrib>Thurnham, David I. ; Mburu, Anne S. W. ; Mwaniki, David L. ; Muniu, Erastus M. ; Alumasa, Fred ; de Wagt, Arjan</creatorcontrib><description>Inflammation influences the assessment of nutritional status. For example, inflammation reduces plasma retinol concentrations and vitamin A deficiency is overestimated. Conversely inflammation increases plasma ferritin concentrations and Fe deficiency is underestimated. Blood samples were obtained from 163 free-living HIV-1-infected adults, not on continuous medication, anti-retroviral drugs or micronutrients, not unwell and who had not reached WHO stage IV of HIV/AIDS. We used four markers of inflammation, C-reactive protein (CRP), α1-acid glycoprotein (AGP), α1-antichymotrypsin and erythrocyte sedimentation rate but mainly CRP and AGP were used to separate the subjects into four groups: ‘healthy’ where both CRP and AGP were normal; ‘incubation phase’ where CRP was elevated; ‘early convalescence’ where AGP and CRP were elevated and ‘late convalescence’ where only AGP was elevated. Correction factors were calculated to remove the influence of inflammation from each biomarker and group where inflammation was present and the data are shown before and after recalculation. The correction increased median plasma retinol concentrations of the whole group from 1·16 to 1·33 μmol/l, comparable with values (mean 1·29 μmol/l) in HIV-negative Kenyan women. Median ferritin concentrations fell by about 50 % in both sexes and the number of women with plasma ferritin concentrations ≤ 12 μg/l increased from eleven to twenty. The correction also increased plasma carotenoids and Hb but not α-tocopherol concentrations. We suggest that the method described to remove the influence of inflammation from nutritional biomarkers should be generally applicable in apparently healthy people and prevents discarding valuable data because of mild inflammation. The method does now need to be tested in other populations.</description><identifier>ISSN: 0007-1145</identifier><identifier>EISSN: 1475-2662</identifier><identifier>DOI: 10.1017/S0007114507883012</identifier><identifier>PMID: 18177514</identifier><identifier>CODEN: BJNUAV</identifier><language>eng</language><publisher>Cambridge, UK: Cambridge University Press</publisher><subject>Acquired immune deficiency syndrome ; Acute-phase proteins ; Acute-Phase Proteins - analysis ; Adolescent ; Adult ; adults ; AIDS ; alpha1-acid glycoprotein ; alpha1-antichymotrypsin ; Biological and medical sciences ; Biomarkers ; Biomarkers - blood ; blood chemistry ; Blood Sedimentation ; C-reactive protein ; calibration ; Carotenoids ; Data analysis ; Erythrocytes ; Feeding. Feeding behavior ; Female ; Ferritin ; Ferritins - blood ; Fundamental and applied biological sciences. Psychology ; glycoproteins ; HIV infections ; HIV Infections - blood ; HIV-1 ; Human immunodeficiency virus 1 ; Humans ; inflammation ; Inflammation Mediators - blood ; Laboratories ; Male ; Methods ; Micronutrients ; nutrient deficiencies ; Nutrition ; Nutrition Assessment ; Nutritional Status ; Sexually transmitted diseases ; Shipments ; STD ; Studies ; validity ; Vertebrates: anatomy and physiology, studies on body, several organs or systems ; Vitamin A ; Vitamin A - blood ; Vitamin A status</subject><ispartof>British journal of nutrition, 2008-07, Vol.100 (1), p.174-182</ispartof><rights>Copyright © The Authors 2008</rights><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c571t-8b660d85bf5e903df679c97430758cfa6be6a803a8bed8feec68fb24f5c80bad3</citedby><cites>FETCH-LOGICAL-c571t-8b660d85bf5e903df679c97430758cfa6be6a803a8bed8feec68fb24f5c80bad3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.cambridge.org/core/product/identifier/S0007114507883012/type/journal_article$$EHTML$$P50$$Gcambridge$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,72960</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20418986$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18177514$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Thurnham, David I.</creatorcontrib><creatorcontrib>Mburu, Anne S. W.</creatorcontrib><creatorcontrib>Mwaniki, David L.</creatorcontrib><creatorcontrib>Muniu, Erastus M.</creatorcontrib><creatorcontrib>Alumasa, Fred</creatorcontrib><creatorcontrib>de Wagt, Arjan</creatorcontrib><title>Using plasma acute-phase protein concentrations to interpret nutritional biomarkers in apparently healthy HIV-1-seropositive Kenyan adults</title><title>British journal of nutrition</title><addtitle>Br J Nutr</addtitle><description>Inflammation influences the assessment of nutritional status. For example, inflammation reduces plasma retinol concentrations and vitamin A deficiency is overestimated. Conversely inflammation increases plasma ferritin concentrations and Fe deficiency is underestimated. Blood samples were obtained from 163 free-living HIV-1-infected adults, not on continuous medication, anti-retroviral drugs or micronutrients, not unwell and who had not reached WHO stage IV of HIV/AIDS. We used four markers of inflammation, C-reactive protein (CRP), α1-acid glycoprotein (AGP), α1-antichymotrypsin and erythrocyte sedimentation rate but mainly CRP and AGP were used to separate the subjects into four groups: ‘healthy’ where both CRP and AGP were normal; ‘incubation phase’ where CRP was elevated; ‘early convalescence’ where AGP and CRP were elevated and ‘late convalescence’ where only AGP was elevated. Correction factors were calculated to remove the influence of inflammation from each biomarker and group where inflammation was present and the data are shown before and after recalculation. The correction increased median plasma retinol concentrations of the whole group from 1·16 to 1·33 μmol/l, comparable with values (mean 1·29 μmol/l) in HIV-negative Kenyan women. Median ferritin concentrations fell by about 50 % in both sexes and the number of women with plasma ferritin concentrations ≤ 12 μg/l increased from eleven to twenty. The correction also increased plasma carotenoids and Hb but not α-tocopherol concentrations. We suggest that the method described to remove the influence of inflammation from nutritional biomarkers should be generally applicable in apparently healthy people and prevents discarding valuable data because of mild inflammation. The method does now need to be tested in other populations.</description><subject>Acquired immune deficiency syndrome</subject><subject>Acute-phase proteins</subject><subject>Acute-Phase Proteins - analysis</subject><subject>Adolescent</subject><subject>Adult</subject><subject>adults</subject><subject>AIDS</subject><subject>alpha1-acid glycoprotein</subject><subject>alpha1-antichymotrypsin</subject><subject>Biological and medical sciences</subject><subject>Biomarkers</subject><subject>Biomarkers - blood</subject><subject>blood chemistry</subject><subject>Blood Sedimentation</subject><subject>C-reactive protein</subject><subject>calibration</subject><subject>Carotenoids</subject><subject>Data analysis</subject><subject>Erythrocytes</subject><subject>Feeding. Feeding behavior</subject><subject>Female</subject><subject>Ferritin</subject><subject>Ferritins - blood</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>glycoproteins</subject><subject>HIV infections</subject><subject>HIV Infections - blood</subject><subject>HIV-1</subject><subject>Human immunodeficiency virus 1</subject><subject>Humans</subject><subject>inflammation</subject><subject>Inflammation Mediators - blood</subject><subject>Laboratories</subject><subject>Male</subject><subject>Methods</subject><subject>Micronutrients</subject><subject>nutrient deficiencies</subject><subject>Nutrition</subject><subject>Nutrition Assessment</subject><subject>Nutritional Status</subject><subject>Sexually transmitted diseases</subject><subject>Shipments</subject><subject>STD</subject><subject>Studies</subject><subject>validity</subject><subject>Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><subject>Vitamin A</subject><subject>Vitamin A - blood</subject><subject>Vitamin A status</subject><issn>0007-1145</issn><issn>1475-2662</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNp1kc9u1DAYxCMEokvhAbiAhQS3gJ0_tnOsKmhLKxBqF3Gzvjhfdl0SO9gOYl-Bp8arjVoJxMmy5zcjjSfLnjP6llEm3l1TSgVjVU2FlCVlxYNsxSpR5wXnxcNstZfzvX6UPQnhNl0lo83j7IhJJkTNqlX2ex2M3ZBpgDACAT1HzKctBCSTdxGNJdpZjTZ6iMbZQKIjxkb0k8dI7By92b_DQFrjRvDf0YcEEJgm8Mk27MgWYYjbHTm_-JqzPKB3kwvJ9RPJJdodJLibhxieZo96GAI-W87jbP3h_c3peX71-ezi9OQq17VgMZct57STddvX2NCy67lodCOqkopa6h54ixwkLUG22MkeUXPZt0XV11rSFrryOHtzyE0Nf8wYohpN0DgMYNHNQQnGi6YpqwS--gu8dbNPXYMqWCkLyaVIEDtA2rsQPPZq8iZ9xE4xqvYrqX9WSp4XS_DcjtjdO5ZZEvB6ASBoGHoPVptwxxW0YrKRPHH5gTMh4q87Pc2guChFrfjZF_VJNpc3H6tGfUv8ywPfg1Ow8SlzfV1QVlLaMJEiE1EudWBsvek2eF_6_4X-AKdHxJc</recordid><startdate>20080701</startdate><enddate>20080701</enddate><creator>Thurnham, David I.</creator><creator>Mburu, Anne S. 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W.</au><au>Mwaniki, David L.</au><au>Muniu, Erastus M.</au><au>Alumasa, Fred</au><au>de Wagt, Arjan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Using plasma acute-phase protein concentrations to interpret nutritional biomarkers in apparently healthy HIV-1-seropositive Kenyan adults</atitle><jtitle>British journal of nutrition</jtitle><addtitle>Br J Nutr</addtitle><date>2008-07-01</date><risdate>2008</risdate><volume>100</volume><issue>1</issue><spage>174</spage><epage>182</epage><pages>174-182</pages><issn>0007-1145</issn><eissn>1475-2662</eissn><coden>BJNUAV</coden><abstract>Inflammation influences the assessment of nutritional status. For example, inflammation reduces plasma retinol concentrations and vitamin A deficiency is overestimated. Conversely inflammation increases plasma ferritin concentrations and Fe deficiency is underestimated. Blood samples were obtained from 163 free-living HIV-1-infected adults, not on continuous medication, anti-retroviral drugs or micronutrients, not unwell and who had not reached WHO stage IV of HIV/AIDS. We used four markers of inflammation, C-reactive protein (CRP), α1-acid glycoprotein (AGP), α1-antichymotrypsin and erythrocyte sedimentation rate but mainly CRP and AGP were used to separate the subjects into four groups: ‘healthy’ where both CRP and AGP were normal; ‘incubation phase’ where CRP was elevated; ‘early convalescence’ where AGP and CRP were elevated and ‘late convalescence’ where only AGP was elevated. Correction factors were calculated to remove the influence of inflammation from each biomarker and group where inflammation was present and the data are shown before and after recalculation. The correction increased median plasma retinol concentrations of the whole group from 1·16 to 1·33 μmol/l, comparable with values (mean 1·29 μmol/l) in HIV-negative Kenyan women. Median ferritin concentrations fell by about 50 % in both sexes and the number of women with plasma ferritin concentrations ≤ 12 μg/l increased from eleven to twenty. The correction also increased plasma carotenoids and Hb but not α-tocopherol concentrations. We suggest that the method described to remove the influence of inflammation from nutritional biomarkers should be generally applicable in apparently healthy people and prevents discarding valuable data because of mild inflammation. The method does now need to be tested in other populations.</abstract><cop>Cambridge, UK</cop><pub>Cambridge University Press</pub><pmid>18177514</pmid><doi>10.1017/S0007114507883012</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acquired immune deficiency syndrome Acute-phase proteins Acute-Phase Proteins - analysis Adolescent Adult adults AIDS alpha1-acid glycoprotein alpha1-antichymotrypsin Biological and medical sciences Biomarkers Biomarkers - blood blood chemistry Blood Sedimentation C-reactive protein calibration Carotenoids Data analysis Erythrocytes Feeding. Feeding behavior Female Ferritin Ferritins - blood Fundamental and applied biological sciences. Psychology glycoproteins HIV infections HIV Infections - blood HIV-1 Human immunodeficiency virus 1 Humans inflammation Inflammation Mediators - blood Laboratories Male Methods Micronutrients nutrient deficiencies Nutrition Nutrition Assessment Nutritional Status Sexually transmitted diseases Shipments STD Studies validity Vertebrates: anatomy and physiology, studies on body, several organs or systems Vitamin A Vitamin A - blood Vitamin A status |
title | Using plasma acute-phase protein concentrations to interpret nutritional biomarkers in apparently healthy HIV-1-seropositive Kenyan adults |
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