Calprotectin as a Biomarker for Melioidosis Disease Progression and Management
Melioidosis is a neglected tropical disease that is caused by the bacterium and is underreported in many countries where the disease is endemic. A long and costly administration of antibiotics is needed to clear infections, and there is an unmet need for biomarkers to guide antibiotic treatment and...
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Veröffentlicht in: | Journal of clinical microbiology 2017-04, Vol.55 (4), p.1205-1210 |
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creator | Natesan, Mohan Corea, Enoka Krishnananthasivam, Shivankari Sathkumara, Harindra Darshana Dankmeyer, Jennifer L Dyas, Beverly K Amemiya, Kei De Silva, Aruna Dharshan Ulrich, Robert G |
description | Melioidosis is a neglected tropical disease that is caused by the bacterium
and is underreported in many countries where the disease is endemic. A long and costly administration of antibiotics is needed to clear infections, and there is an unmet need for biomarkers to guide antibiotic treatment and increase the number of patients that complete therapy. We identified calprotectin as a lead biomarker of
infections and examined correlations between this serum protein and the antibiotic treatment outcomes of patients with melioidosis. Serum levels of calprotectin and C-reactive protein were significantly higher in patients with melioidosis and nonmelioidosis sepsis than in healthy controls. Median calprotectin levels were higher in patients with melioidosis than in those with nonmelioidosis sepsis, whereas C-reactive protein levels were similar in both groups. Notably, intensive intravenous antibiotic treatment of patients with melioidosis resulted in lower levels of calprotectin and C-reactive protein (
< 0.0001), coinciding with recovery. The median percent reduction of calprotectin and C-reactive protein was 71% for both biomarkers after antibacterial therapy. In contrast, we found no significant differences in calreticulin levels between the two melioidosis treatment phases. Thus, reductions in serum calprotectin levels were linked to therapeutic responses to antibiotics. Our results suggest that calprotectin may be a sensitive indicator of melioidosis disease activity and illustrate the potential utility of this biomarker in guiding the duration of antibiotic therapy. |
doi_str_mv | 10.1128/JCM.02284-16 |
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and is underreported in many countries where the disease is endemic. A long and costly administration of antibiotics is needed to clear infections, and there is an unmet need for biomarkers to guide antibiotic treatment and increase the number of patients that complete therapy. We identified calprotectin as a lead biomarker of
infections and examined correlations between this serum protein and the antibiotic treatment outcomes of patients with melioidosis. Serum levels of calprotectin and C-reactive protein were significantly higher in patients with melioidosis and nonmelioidosis sepsis than in healthy controls. Median calprotectin levels were higher in patients with melioidosis than in those with nonmelioidosis sepsis, whereas C-reactive protein levels were similar in both groups. Notably, intensive intravenous antibiotic treatment of patients with melioidosis resulted in lower levels of calprotectin and C-reactive protein (
< 0.0001), coinciding with recovery. The median percent reduction of calprotectin and C-reactive protein was 71% for both biomarkers after antibacterial therapy. In contrast, we found no significant differences in calreticulin levels between the two melioidosis treatment phases. Thus, reductions in serum calprotectin levels were linked to therapeutic responses to antibiotics. Our results suggest that calprotectin may be a sensitive indicator of melioidosis disease activity and illustrate the potential utility of this biomarker in guiding the duration of antibiotic therapy.</description><identifier>ISSN: 0095-1137</identifier><identifier>EISSN: 1098-660X</identifier><identifier>DOI: 10.1128/JCM.02284-16</identifier><identifier>PMID: 28179407</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Administration, Intravenous ; Adolescent ; Adult ; Aged ; Anti-Bacterial Agents - administration & dosage ; Bacteriology ; Biomarkers - blood ; Burkholderia pseudomallei ; C-Reactive Protein - analysis ; Cohort Studies ; Disease Progression ; Drug Monitoring - methods ; Female ; Humans ; Leukocyte L1 Antigen Complex - blood ; Male ; Melioidosis - diagnosis ; Melioidosis - drug therapy ; Middle Aged ; Pregnancy ; Serum - chemistry ; Young Adult</subject><ispartof>Journal of clinical microbiology, 2017-04, Vol.55 (4), p.1205-1210</ispartof><rights>Copyright © 2017 American Society for Microbiology.</rights><rights>Copyright © 2017 American Society for Microbiology. 2017 American Society for Microbiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c417t-66ed1e9fba2654efee76d573a4f86943e7f8d1fb5f3a9bc1b3babf7691c522483</citedby><cites>FETCH-LOGICAL-c417t-66ed1e9fba2654efee76d573a4f86943e7f8d1fb5f3a9bc1b3babf7691c522483</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/PMC5377848/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5377848/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,3175,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28179407$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Onderdonk, Andrew B.</contributor><creatorcontrib>Natesan, Mohan</creatorcontrib><creatorcontrib>Corea, Enoka</creatorcontrib><creatorcontrib>Krishnananthasivam, Shivankari</creatorcontrib><creatorcontrib>Sathkumara, Harindra Darshana</creatorcontrib><creatorcontrib>Dankmeyer, Jennifer L</creatorcontrib><creatorcontrib>Dyas, Beverly K</creatorcontrib><creatorcontrib>Amemiya, Kei</creatorcontrib><creatorcontrib>De Silva, Aruna Dharshan</creatorcontrib><creatorcontrib>Ulrich, Robert G</creatorcontrib><title>Calprotectin as a Biomarker for Melioidosis Disease Progression and Management</title><title>Journal of clinical microbiology</title><addtitle>J Clin Microbiol</addtitle><description>Melioidosis is a neglected tropical disease that is caused by the bacterium
and is underreported in many countries where the disease is endemic. A long and costly administration of antibiotics is needed to clear infections, and there is an unmet need for biomarkers to guide antibiotic treatment and increase the number of patients that complete therapy. We identified calprotectin as a lead biomarker of
infections and examined correlations between this serum protein and the antibiotic treatment outcomes of patients with melioidosis. Serum levels of calprotectin and C-reactive protein were significantly higher in patients with melioidosis and nonmelioidosis sepsis than in healthy controls. Median calprotectin levels were higher in patients with melioidosis than in those with nonmelioidosis sepsis, whereas C-reactive protein levels were similar in both groups. Notably, intensive intravenous antibiotic treatment of patients with melioidosis resulted in lower levels of calprotectin and C-reactive protein (
< 0.0001), coinciding with recovery. The median percent reduction of calprotectin and C-reactive protein was 71% for both biomarkers after antibacterial therapy. In contrast, we found no significant differences in calreticulin levels between the two melioidosis treatment phases. Thus, reductions in serum calprotectin levels were linked to therapeutic responses to antibiotics. Our results suggest that calprotectin may be a sensitive indicator of melioidosis disease activity and illustrate the potential utility of this biomarker in guiding the duration of antibiotic therapy.</description><subject>Administration, Intravenous</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Anti-Bacterial Agents - administration & dosage</subject><subject>Bacteriology</subject><subject>Biomarkers - blood</subject><subject>Burkholderia pseudomallei</subject><subject>C-Reactive Protein - analysis</subject><subject>Cohort Studies</subject><subject>Disease Progression</subject><subject>Drug Monitoring - methods</subject><subject>Female</subject><subject>Humans</subject><subject>Leukocyte L1 Antigen Complex - blood</subject><subject>Male</subject><subject>Melioidosis - diagnosis</subject><subject>Melioidosis - drug therapy</subject><subject>Middle Aged</subject><subject>Pregnancy</subject><subject>Serum - chemistry</subject><subject>Young Adult</subject><issn>0095-1137</issn><issn>1098-660X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkb1PHDEQxS0Eyh0kHTXakiILnrXXHw0SuQABcUmKRKKzvLvji8Pe-mLvIfHfYz5ygo5qivnNm_f0CNkHegRQqeOr2fyIVpXiJYgtMgWqVSkEvdkmU0p1XQIwOSG7Kf2lFDiv6w9kUimQmlM5Jd9ntl_FMGI7-qGwqbDFFx-WNt5iLFyIxRx7H3wXkk_FV5_QJix-xrCImJIP-WToirkd7AKXOIwfyY6zfcJPL3OP_D4_-zX7Vl7_uLicnV6XLQc5Zn_YAWrX2ErUHB2iFF0tmeVOCc0ZSqc6cE3tmNVNCw1rbOOk0NDWVcUV2yMnz7qrdbPErs2vo-3NKvps_d4E683bzeD_mEW4MzWTUj0JHL4IxPBvjWk0S59a7Hs7YFgnA0pLpjLM34EKITTLwTL6-RltY0gpots4Amoe2zK5LfPUlgGR8YPXKTbw_3rYAwuMkWo</recordid><startdate>20170401</startdate><enddate>20170401</enddate><creator>Natesan, Mohan</creator><creator>Corea, Enoka</creator><creator>Krishnananthasivam, Shivankari</creator><creator>Sathkumara, Harindra Darshana</creator><creator>Dankmeyer, Jennifer L</creator><creator>Dyas, Beverly K</creator><creator>Amemiya, Kei</creator><creator>De Silva, Aruna Dharshan</creator><creator>Ulrich, Robert G</creator><general>American Society for Microbiology</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>7X8</scope><scope>7QL</scope><scope>C1K</scope><scope>5PM</scope></search><sort><creationdate>20170401</creationdate><title>Calprotectin as a Biomarker for Melioidosis Disease Progression and Management</title><author>Natesan, Mohan ; Corea, Enoka ; Krishnananthasivam, Shivankari ; Sathkumara, Harindra Darshana ; Dankmeyer, Jennifer L ; Dyas, Beverly K ; Amemiya, Kei ; De Silva, Aruna Dharshan ; Ulrich, Robert G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c417t-66ed1e9fba2654efee76d573a4f86943e7f8d1fb5f3a9bc1b3babf7691c522483</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Administration, Intravenous</topic><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Anti-Bacterial Agents - administration & dosage</topic><topic>Bacteriology</topic><topic>Biomarkers - blood</topic><topic>Burkholderia pseudomallei</topic><topic>C-Reactive Protein - analysis</topic><topic>Cohort Studies</topic><topic>Disease Progression</topic><topic>Drug Monitoring - methods</topic><topic>Female</topic><topic>Humans</topic><topic>Leukocyte L1 Antigen Complex - blood</topic><topic>Male</topic><topic>Melioidosis - diagnosis</topic><topic>Melioidosis - drug therapy</topic><topic>Middle Aged</topic><topic>Pregnancy</topic><topic>Serum - chemistry</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Natesan, Mohan</creatorcontrib><creatorcontrib>Corea, Enoka</creatorcontrib><creatorcontrib>Krishnananthasivam, Shivankari</creatorcontrib><creatorcontrib>Sathkumara, Harindra Darshana</creatorcontrib><creatorcontrib>Dankmeyer, Jennifer L</creatorcontrib><creatorcontrib>Dyas, Beverly K</creatorcontrib><creatorcontrib>Amemiya, Kei</creatorcontrib><creatorcontrib>De Silva, Aruna Dharshan</creatorcontrib><creatorcontrib>Ulrich, Robert G</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Environmental Sciences and Pollution Management</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of clinical microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Natesan, Mohan</au><au>Corea, Enoka</au><au>Krishnananthasivam, Shivankari</au><au>Sathkumara, Harindra Darshana</au><au>Dankmeyer, Jennifer L</au><au>Dyas, Beverly K</au><au>Amemiya, Kei</au><au>De Silva, Aruna Dharshan</au><au>Ulrich, Robert G</au><au>Onderdonk, Andrew B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Calprotectin as a Biomarker for Melioidosis Disease Progression and Management</atitle><jtitle>Journal of clinical microbiology</jtitle><addtitle>J Clin Microbiol</addtitle><date>2017-04-01</date><risdate>2017</risdate><volume>55</volume><issue>4</issue><spage>1205</spage><epage>1210</epage><pages>1205-1210</pages><issn>0095-1137</issn><eissn>1098-660X</eissn><abstract>Melioidosis is a neglected tropical disease that is caused by the bacterium
and is underreported in many countries where the disease is endemic. A long and costly administration of antibiotics is needed to clear infections, and there is an unmet need for biomarkers to guide antibiotic treatment and increase the number of patients that complete therapy. We identified calprotectin as a lead biomarker of
infections and examined correlations between this serum protein and the antibiotic treatment outcomes of patients with melioidosis. Serum levels of calprotectin and C-reactive protein were significantly higher in patients with melioidosis and nonmelioidosis sepsis than in healthy controls. Median calprotectin levels were higher in patients with melioidosis than in those with nonmelioidosis sepsis, whereas C-reactive protein levels were similar in both groups. Notably, intensive intravenous antibiotic treatment of patients with melioidosis resulted in lower levels of calprotectin and C-reactive protein (
< 0.0001), coinciding with recovery. The median percent reduction of calprotectin and C-reactive protein was 71% for both biomarkers after antibacterial therapy. In contrast, we found no significant differences in calreticulin levels between the two melioidosis treatment phases. Thus, reductions in serum calprotectin levels were linked to therapeutic responses to antibiotics. Our results suggest that calprotectin may be a sensitive indicator of melioidosis disease activity and illustrate the potential utility of this biomarker in guiding the duration of antibiotic therapy.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>28179407</pmid><doi>10.1128/JCM.02284-16</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Administration, Intravenous Adolescent Adult Aged Anti-Bacterial Agents - administration & dosage Bacteriology Biomarkers - blood Burkholderia pseudomallei C-Reactive Protein - analysis Cohort Studies Disease Progression Drug Monitoring - methods Female Humans Leukocyte L1 Antigen Complex - blood Male Melioidosis - diagnosis Melioidosis - drug therapy Middle Aged Pregnancy Serum - chemistry Young Adult |
title | Calprotectin as a Biomarker for Melioidosis Disease Progression and Management |
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