Haematological changes in Schistosoma haematobium infections in school children in Gabon
Background Schistosomiasis is a parasitic disease affecting the blood cell. As a chronic disease, schistosomiasis particularly impacts on the human host’s haematological profile. We assessed here the impact of urogenital schistosomiasis on the full blood counts (FBC) as proxy diagnostic tool for sch...
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description | Background
Schistosomiasis is a parasitic disease affecting the blood cell. As a chronic disease, schistosomiasis particularly impacts on the human host’s haematological profile. We assessed here the impact of urogenital schistosomiasis on the full blood counts (FBC) as proxy diagnostic tool for schistosomiasis.
Methods
A cross-sectional study was conducted among school children living in Lambaréné, Gabon. Schistosomiasis status was determined using urine filtration technique. EDTA blood samples were analysed using a Pentra ABX 60
®
analyzer.
Results
Compared to their infection-free counterparts, school children infected with
Schistosoma haematobium
displayed an altered FBC profile, with changes in all three blood cell lines. Adjusted for praziquantel intake, soil-transmitted helminthic infections and
Plasmodium falciparum
infection status, schistosomiasis was independently associated with a decreasing trend of mean haemoglobin (β = − 0.20 g/dL,
p-value
= 0.08) and hematocrit (β = − 0.61%,
p-value
= 0.06) levels, a lower mean MCV (β = − 1.50µm
3
,
p-value
= 0.02) and MCH (β = − 0.54 pg,
p-value
= 0.04), and higher platelet (β = 28.2 10
3
/mm
3
,
p-value
= 0.002) and leukocyte (β = 1.13 10
3
/mm
3
,
p-value
= 0.0003) counts, respectively.
Conclusions
Schistosomiasis is associated with a characteristic FBC profile of schoolchildren living in Lambaréné, indicating the necessity to consider schistosomiasis as a single cause of disease, or a co-morbidity, when interpreting FBC in endemic areas. |
doi_str_mv | 10.1007/s15010-020-01575-5 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8316219</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2555484751</sourcerecordid><originalsourceid>FETCH-LOGICAL-c474t-b4239cb921477164376946d7fcf3dc8046ae40c74ddb14345f4e823c5dae7e773</originalsourceid><addsrcrecordid>eNp9kU9LHTEUxUNR6tP2C3RRHrhxM3qT3ExmNgWR-gcEF22hu5DJZN5EZhKbzAj99uY5aqsLFyGQ87vn5nAI-ULhmALIk0QFUCiA5UOFFIX4QFYUeV1ALfkOWQEHKCrKyj2yn9ItAIga5UeyxzlWpaR8RX5fajvqKQxh44we1qbXfmPT2vn1D9O7NIUURr3uF6px85ilzprJBf9IJdOHsJ1zQxut3z5d6Cb4T2S300Oyn5_uA_Lr_PvPs8vi-ubi6uz0ujAocSoaZLw2Tc0oSklL5LKssWxlZzremgqw1BbBSGzbJkdD0aGtGDei1VZaKfkB-bb43s3NaFtj_RT1oO6iG3X8q4J26rXiXa824V5VnJaM1tng6Mkghj-zTZMaXTJ2GLS3YU6KYQUSa8ZZRg_foLdhjj7HU0wIgRVKQTPFFsrEkFK03ctnKKhtcWopTuXi1GNxSuShr__HeBl5bioDfAFSlnJF8d_ud2wfAEWspFI</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2555484751</pqid></control><display><type>article</type><title>Haematological changes in Schistosoma haematobium infections in school children in Gabon</title><source>MEDLINE</source><source>SpringerLink Journals - AutoHoldings</source><creator>Dejon-Agobé, Jean Claude ; Adegnika, Ayôla A. ; Grobusch, Martin P.</creator><creatorcontrib>Dejon-Agobé, Jean Claude ; Adegnika, Ayôla A. ; Grobusch, Martin P.</creatorcontrib><description>Background
Schistosomiasis is a parasitic disease affecting the blood cell. As a chronic disease, schistosomiasis particularly impacts on the human host’s haematological profile. We assessed here the impact of urogenital schistosomiasis on the full blood counts (FBC) as proxy diagnostic tool for schistosomiasis.
Methods
A cross-sectional study was conducted among school children living in Lambaréné, Gabon. Schistosomiasis status was determined using urine filtration technique. EDTA blood samples were analysed using a Pentra ABX 60
®
analyzer.
Results
Compared to their infection-free counterparts, school children infected with
Schistosoma haematobium
displayed an altered FBC profile, with changes in all three blood cell lines. Adjusted for praziquantel intake, soil-transmitted helminthic infections and
Plasmodium falciparum
infection status, schistosomiasis was independently associated with a decreasing trend of mean haemoglobin (β = − 0.20 g/dL,
p-value
= 0.08) and hematocrit (β = − 0.61%,
p-value
= 0.06) levels, a lower mean MCV (β = − 1.50µm
3
,
p-value
= 0.02) and MCH (β = − 0.54 pg,
p-value
= 0.04), and higher platelet (β = 28.2 10
3
/mm
3
,
p-value
= 0.002) and leukocyte (β = 1.13 10
3
/mm
3
,
p-value
= 0.0003) counts, respectively.
Conclusions
Schistosomiasis is associated with a characteristic FBC profile of schoolchildren living in Lambaréné, indicating the necessity to consider schistosomiasis as a single cause of disease, or a co-morbidity, when interpreting FBC in endemic areas.</description><identifier>ISSN: 0300-8126</identifier><identifier>EISSN: 1439-0973</identifier><identifier>DOI: 10.1007/s15010-020-01575-5</identifier><identifier>PMID: 33486713</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Animals ; Blood ; Cell lines ; Child ; Children ; Cross-Sectional Studies ; Ethylenediaminetetraacetic acids ; Family Medicine ; Gabon - epidemiology ; General Practice ; Hematocrit ; Hematology ; Hemoglobin ; Hemoglobins ; Humans ; Infectious Diseases ; Internal Medicine ; Leukocyte Count ; Leukocytes ; Medicine ; Medicine & Public Health ; Morbidity ; Original Paper ; Parasitic diseases ; Pediatrics ; Platelet Count ; Praziquantel ; Prevalence ; Schistosoma haematobium ; Schistosomiasis ; Schistosomiasis haematobia - blood ; Schistosomiasis haematobia - epidemiology ; Schools</subject><ispartof>Infection, 2021-08, Vol.49 (4), p.645-651</ispartof><rights>The Author(s) 2021</rights><rights>2021. The Author(s).</rights><rights>The Author(s) 2021. This work is published 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><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-b4239cb921477164376946d7fcf3dc8046ae40c74ddb14345f4e823c5dae7e773</citedby><cites>FETCH-LOGICAL-c474t-b4239cb921477164376946d7fcf3dc8046ae40c74ddb14345f4e823c5dae7e773</cites><orcidid>0000-0002-0046-1099</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s15010-020-01575-5$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s15010-020-01575-5$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,777,781,882,27905,27906,41469,42538,51300</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33486713$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dejon-Agobé, Jean Claude</creatorcontrib><creatorcontrib>Adegnika, Ayôla A.</creatorcontrib><creatorcontrib>Grobusch, Martin P.</creatorcontrib><title>Haematological changes in Schistosoma haematobium infections in school children in Gabon</title><title>Infection</title><addtitle>Infection</addtitle><addtitle>Infection</addtitle><description>Background
Schistosomiasis is a parasitic disease affecting the blood cell. As a chronic disease, schistosomiasis particularly impacts on the human host’s haematological profile. We assessed here the impact of urogenital schistosomiasis on the full blood counts (FBC) as proxy diagnostic tool for schistosomiasis.
Methods
A cross-sectional study was conducted among school children living in Lambaréné, Gabon. Schistosomiasis status was determined using urine filtration technique. EDTA blood samples were analysed using a Pentra ABX 60
®
analyzer.
Results
Compared to their infection-free counterparts, school children infected with
Schistosoma haematobium
displayed an altered FBC profile, with changes in all three blood cell lines. Adjusted for praziquantel intake, soil-transmitted helminthic infections and
Plasmodium falciparum
infection status, schistosomiasis was independently associated with a decreasing trend of mean haemoglobin (β = − 0.20 g/dL,
p-value
= 0.08) and hematocrit (β = − 0.61%,
p-value
= 0.06) levels, a lower mean MCV (β = − 1.50µm
3
,
p-value
= 0.02) and MCH (β = − 0.54 pg,
p-value
= 0.04), and higher platelet (β = 28.2 10
3
/mm
3
,
p-value
= 0.002) and leukocyte (β = 1.13 10
3
/mm
3
,
p-value
= 0.0003) counts, respectively.
Conclusions
Schistosomiasis is associated with a characteristic FBC profile of schoolchildren living in Lambaréné, indicating the necessity to consider schistosomiasis as a single cause of disease, or a co-morbidity, when interpreting FBC in endemic areas.</description><subject>Animals</subject><subject>Blood</subject><subject>Cell lines</subject><subject>Child</subject><subject>Children</subject><subject>Cross-Sectional Studies</subject><subject>Ethylenediaminetetraacetic acids</subject><subject>Family Medicine</subject><subject>Gabon - epidemiology</subject><subject>General Practice</subject><subject>Hematocrit</subject><subject>Hematology</subject><subject>Hemoglobin</subject><subject>Hemoglobins</subject><subject>Humans</subject><subject>Infectious Diseases</subject><subject>Internal Medicine</subject><subject>Leukocyte Count</subject><subject>Leukocytes</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Morbidity</subject><subject>Original Paper</subject><subject>Parasitic diseases</subject><subject>Pediatrics</subject><subject>Platelet Count</subject><subject>Praziquantel</subject><subject>Prevalence</subject><subject>Schistosoma haematobium</subject><subject>Schistosomiasis</subject><subject>Schistosomiasis haematobia - blood</subject><subject>Schistosomiasis haematobia - epidemiology</subject><subject>Schools</subject><issn>0300-8126</issn><issn>1439-0973</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9kU9LHTEUxUNR6tP2C3RRHrhxM3qT3ExmNgWR-gcEF22hu5DJZN5EZhKbzAj99uY5aqsLFyGQ87vn5nAI-ULhmALIk0QFUCiA5UOFFIX4QFYUeV1ALfkOWQEHKCrKyj2yn9ItAIga5UeyxzlWpaR8RX5fajvqKQxh44we1qbXfmPT2vn1D9O7NIUURr3uF6px85ilzprJBf9IJdOHsJ1zQxut3z5d6Cb4T2S300Oyn5_uA_Lr_PvPs8vi-ubi6uz0ujAocSoaZLw2Tc0oSklL5LKssWxlZzremgqw1BbBSGzbJkdD0aGtGDei1VZaKfkB-bb43s3NaFtj_RT1oO6iG3X8q4J26rXiXa824V5VnJaM1tng6Mkghj-zTZMaXTJ2GLS3YU6KYQUSa8ZZRg_foLdhjj7HU0wIgRVKQTPFFsrEkFK03ctnKKhtcWopTuXi1GNxSuShr__HeBl5bioDfAFSlnJF8d_ud2wfAEWspFI</recordid><startdate>20210801</startdate><enddate>20210801</enddate><creator>Dejon-Agobé, Jean Claude</creator><creator>Adegnika, Ayôla A.</creator><creator>Grobusch, Martin P.</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>C6C</scope><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>7QL</scope><scope>7RV</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>NAPCQ</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-0046-1099</orcidid></search><sort><creationdate>20210801</creationdate><title>Haematological changes in Schistosoma haematobium infections in school children in Gabon</title><author>Dejon-Agobé, Jean Claude ; Adegnika, Ayôla A. ; Grobusch, Martin P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-b4239cb921477164376946d7fcf3dc8046ae40c74ddb14345f4e823c5dae7e773</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Animals</topic><topic>Blood</topic><topic>Cell lines</topic><topic>Child</topic><topic>Children</topic><topic>Cross-Sectional Studies</topic><topic>Ethylenediaminetetraacetic acids</topic><topic>Family Medicine</topic><topic>Gabon - epidemiology</topic><topic>General Practice</topic><topic>Hematocrit</topic><topic>Hematology</topic><topic>Hemoglobin</topic><topic>Hemoglobins</topic><topic>Humans</topic><topic>Infectious Diseases</topic><topic>Internal Medicine</topic><topic>Leukocyte Count</topic><topic>Leukocytes</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Morbidity</topic><topic>Original Paper</topic><topic>Parasitic diseases</topic><topic>Pediatrics</topic><topic>Platelet Count</topic><topic>Praziquantel</topic><topic>Prevalence</topic><topic>Schistosoma haematobium</topic><topic>Schistosomiasis</topic><topic>Schistosomiasis haematobia - blood</topic><topic>Schistosomiasis haematobia - epidemiology</topic><topic>Schools</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dejon-Agobé, Jean Claude</creatorcontrib><creatorcontrib>Adegnika, Ayôla A.</creatorcontrib><creatorcontrib>Grobusch, Martin P.</creatorcontrib><collection>Springer Nature OA/Free Journals</collection><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>Bacteriology Abstracts (Microbiology B)</collection><collection>Nursing & Allied Health Database</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</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 Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Infection</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dejon-Agobé, Jean Claude</au><au>Adegnika, Ayôla A.</au><au>Grobusch, Martin P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Haematological changes in Schistosoma haematobium infections in school children in Gabon</atitle><jtitle>Infection</jtitle><stitle>Infection</stitle><addtitle>Infection</addtitle><date>2021-08-01</date><risdate>2021</risdate><volume>49</volume><issue>4</issue><spage>645</spage><epage>651</epage><pages>645-651</pages><issn>0300-8126</issn><eissn>1439-0973</eissn><abstract>Background
Schistosomiasis is a parasitic disease affecting the blood cell. As a chronic disease, schistosomiasis particularly impacts on the human host’s haematological profile. We assessed here the impact of urogenital schistosomiasis on the full blood counts (FBC) as proxy diagnostic tool for schistosomiasis.
Methods
A cross-sectional study was conducted among school children living in Lambaréné, Gabon. Schistosomiasis status was determined using urine filtration technique. EDTA blood samples were analysed using a Pentra ABX 60
®
analyzer.
Results
Compared to their infection-free counterparts, school children infected with
Schistosoma haematobium
displayed an altered FBC profile, with changes in all three blood cell lines. Adjusted for praziquantel intake, soil-transmitted helminthic infections and
Plasmodium falciparum
infection status, schistosomiasis was independently associated with a decreasing trend of mean haemoglobin (β = − 0.20 g/dL,
p-value
= 0.08) and hematocrit (β = − 0.61%,
p-value
= 0.06) levels, a lower mean MCV (β = − 1.50µm
3
,
p-value
= 0.02) and MCH (β = − 0.54 pg,
p-value
= 0.04), and higher platelet (β = 28.2 10
3
/mm
3
,
p-value
= 0.002) and leukocyte (β = 1.13 10
3
/mm
3
,
p-value
= 0.0003) counts, respectively.
Conclusions
Schistosomiasis is associated with a characteristic FBC profile of schoolchildren living in Lambaréné, indicating the necessity to consider schistosomiasis as a single cause of disease, or a co-morbidity, when interpreting FBC in endemic areas.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>33486713</pmid><doi>10.1007/s15010-020-01575-5</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-0046-1099</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals Blood Cell lines Child Children Cross-Sectional Studies Ethylenediaminetetraacetic acids Family Medicine Gabon - epidemiology General Practice Hematocrit Hematology Hemoglobin Hemoglobins Humans Infectious Diseases Internal Medicine Leukocyte Count Leukocytes Medicine Medicine & Public Health Morbidity Original Paper Parasitic diseases Pediatrics Platelet Count Praziquantel Prevalence Schistosoma haematobium Schistosomiasis Schistosomiasis haematobia - blood Schistosomiasis haematobia - epidemiology Schools |
title | Haematological changes in Schistosoma haematobium infections in school children in Gabon |
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