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Serum intact fibroblast growth factor 23 in healthy paediatric population
It is believed that fibroblast growth factor 23 (FGF23) can become an early biomarker of chronic kidney disease progression. Data on FGF23 age dependency are inconsistent. We present the results of the cross-sectional study concerning FGF23 levels in healthy Polish children. This study was conducted...
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Published in: | Open medicine (Warsaw, Poland) Poland), 2021-07, Vol.16 (1), p.1022-1027 |
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description | It is believed that fibroblast growth factor 23 (FGF23) can become an early biomarker of chronic kidney disease progression. Data on FGF23 age dependency are inconsistent. We present the results of the cross-sectional study concerning FGF23 levels in healthy Polish children.
This study was conducted in 121 children aged 0-18 years. Kidney function and intact FGF23 levels in serum were assessed. Differences between age groups and according to gender were analysed.
The difference in FGF23 between age groups and according to gender was statistically insignificant. In the youngest and the oldest group, a trend to higher FGF23 levels was observed. FGF23 level in girls tended to be higher than boys, apart from the age group between 1 and 4 years. There was a negative correlation between eGFR and FGF23 (
= -0.26,
< 0.05) - strong in girls (
= -0.38,
< 0.05), but not in boys. In each age group, we found no significant correlation between eGFR and FGF23.
Our study supports the evidence that the FGF23 level in paediatric population is not age or sex dependent. The results can serve as a reference point under clinical conditions and for other studies on the topic. |
doi_str_mv | 10.1515/med-2021-0288 |
format | article |
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This study was conducted in 121 children aged 0-18 years. Kidney function and intact FGF23 levels in serum were assessed. Differences between age groups and according to gender were analysed.
The difference in FGF23 between age groups and according to gender was statistically insignificant. In the youngest and the oldest group, a trend to higher FGF23 levels was observed. FGF23 level in girls tended to be higher than boys, apart from the age group between 1 and 4 years. There was a negative correlation between eGFR and FGF23 (
= -0.26,
< 0.05) - strong in girls (
= -0.38,
< 0.05), but not in boys. In each age group, we found no significant correlation between eGFR and FGF23.
Our study supports the evidence that the FGF23 level in paediatric population is not age or sex dependent. The results can serve as a reference point under clinical conditions and for other studies on the topic.</description><identifier>ISSN: 2391-5463</identifier><identifier>EISSN: 2391-5463</identifier><identifier>DOI: 10.1515/med-2021-0288</identifier><identifier>PMID: 34258392</identifier><language>eng</language><publisher>Poland: De Gruyter</publisher><subject>Age groups ; child ; fibroblast growth factors ; Fibroblasts ; Growth factors ; Pediatrics ; renal insufficiency</subject><ispartof>Open medicine (Warsaw, Poland), 2021-07, Vol.16 (1), p.1022-1027</ispartof><rights>2021 Malgorzata Stanczyk et al., published by De Gruyter.</rights><rights>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><rights>2021 Malgorzata Stanczyk ., published by De Gruyter 2021 Malgorzata Stanczyk et al., published by De Gruyter</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c464t-2360feaa94858d3a10b8b79fca1ee0fb5491d7069dfe404023e26a9b163cfae73</citedby><cites>FETCH-LOGICAL-c464t-2360feaa94858d3a10b8b79fca1ee0fb5491d7069dfe404023e26a9b163cfae73</cites><orcidid>0000-0001-6613-1642</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/PMC8262519/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8262519/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53769,53771,66904,68688</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34258392$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Stanczyk, Malgorzata</creatorcontrib><creatorcontrib>Chrul, Slawomir</creatorcontrib><creatorcontrib>Wyka, Krystyna</creatorcontrib><creatorcontrib>Tkaczyk, Marcin</creatorcontrib><title>Serum intact fibroblast growth factor 23 in healthy paediatric population</title><title>Open medicine (Warsaw, Poland)</title><addtitle>Open Med (Wars)</addtitle><description>It is believed that fibroblast growth factor 23 (FGF23) can become an early biomarker of chronic kidney disease progression. Data on FGF23 age dependency are inconsistent. We present the results of the cross-sectional study concerning FGF23 levels in healthy Polish children.
This study was conducted in 121 children aged 0-18 years. Kidney function and intact FGF23 levels in serum were assessed. Differences between age groups and according to gender were analysed.
The difference in FGF23 between age groups and according to gender was statistically insignificant. In the youngest and the oldest group, a trend to higher FGF23 levels was observed. FGF23 level in girls tended to be higher than boys, apart from the age group between 1 and 4 years. There was a negative correlation between eGFR and FGF23 (
= -0.26,
< 0.05) - strong in girls (
= -0.38,
< 0.05), but not in boys. In each age group, we found no significant correlation between eGFR and FGF23.
Our study supports the evidence that the FGF23 level in paediatric population is not age or sex dependent. The results can serve as a reference point under clinical conditions and for other studies on the topic.</description><subject>Age groups</subject><subject>child</subject><subject>fibroblast growth factors</subject><subject>Fibroblasts</subject><subject>Growth factors</subject><subject>Pediatrics</subject><subject>renal insufficiency</subject><issn>2391-5463</issn><issn>2391-5463</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNptkU2LFDEQhhtR3GXdo1dp8OKlNV_dSUAEWfwYWPCgnkN1ujKToafTJmmX-femnXXdFU8pkoe3KvVU1XNKXtOWtm8OODSMMNoQptSj6pxxTZtWdPzxvfqsukxpTwihLZdakqfVGResVVyz82rzFeNyqP2Uweba-T6GfoSU620MN3lXu3IdYs14Qeodwph3x3oGHDzk6G09h3kZIfswPaueOBgTXt6eF9X3jx--XX1urr982ly9v26s6ERuGO-IQwAtVKsGDpT0qpfaWaCIxPWt0HSQpNODQ0EEYRxZB7qnHbcOUPKLanPKHQLszRz9AeLRBPDm90WIWwMxezuiEVI6RwgMVK3trEJA4figqXVSqr5kvTtlzUtfdmlxyhHGB6EPXya_M9vw0yjWsZbqEvDqNiCGHwumbA4-WRxHmDAsybC2aJKqYyv68h90H5Y4lVUVSigpih5WqOZE2RhSiujuhqHErM5Nmcaszs3qvPAv7v_gjv5juABvT8BNcYdxwG1cjqX42_2_wbSjlDDGfwGIabsp</recordid><startdate>20210706</startdate><enddate>20210706</enddate><creator>Stanczyk, Malgorzata</creator><creator>Chrul, Slawomir</creator><creator>Wyka, Krystyna</creator><creator>Tkaczyk, Marcin</creator><general>De Gruyter</general><general>Walter de Gruyter GmbH</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</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/0000-0001-6613-1642</orcidid></search><sort><creationdate>20210706</creationdate><title>Serum intact fibroblast growth factor 23 in healthy paediatric population</title><author>Stanczyk, Malgorzata ; Chrul, Slawomir ; Wyka, Krystyna ; Tkaczyk, Marcin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c464t-2360feaa94858d3a10b8b79fca1ee0fb5491d7069dfe404023e26a9b163cfae73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Age groups</topic><topic>child</topic><topic>fibroblast growth factors</topic><topic>Fibroblasts</topic><topic>Growth factors</topic><topic>Pediatrics</topic><topic>renal insufficiency</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stanczyk, Malgorzata</creatorcontrib><creatorcontrib>Chrul, Slawomir</creatorcontrib><creatorcontrib>Wyka, Krystyna</creatorcontrib><creatorcontrib>Tkaczyk, Marcin</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest Pharma 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 UK/Ireland</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</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>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>Open medicine (Warsaw, Poland)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stanczyk, Malgorzata</au><au>Chrul, Slawomir</au><au>Wyka, Krystyna</au><au>Tkaczyk, Marcin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Serum intact fibroblast growth factor 23 in healthy paediatric population</atitle><jtitle>Open medicine (Warsaw, Poland)</jtitle><addtitle>Open Med (Wars)</addtitle><date>2021-07-06</date><risdate>2021</risdate><volume>16</volume><issue>1</issue><spage>1022</spage><epage>1027</epage><pages>1022-1027</pages><issn>2391-5463</issn><eissn>2391-5463</eissn><abstract>It is believed that fibroblast growth factor 23 (FGF23) can become an early biomarker of chronic kidney disease progression. Data on FGF23 age dependency are inconsistent. We present the results of the cross-sectional study concerning FGF23 levels in healthy Polish children.
This study was conducted in 121 children aged 0-18 years. Kidney function and intact FGF23 levels in serum were assessed. Differences between age groups and according to gender were analysed.
The difference in FGF23 between age groups and according to gender was statistically insignificant. In the youngest and the oldest group, a trend to higher FGF23 levels was observed. FGF23 level in girls tended to be higher than boys, apart from the age group between 1 and 4 years. There was a negative correlation between eGFR and FGF23 (
= -0.26,
< 0.05) - strong in girls (
= -0.38,
< 0.05), but not in boys. In each age group, we found no significant correlation between eGFR and FGF23.
Our study supports the evidence that the FGF23 level in paediatric population is not age or sex dependent. The results can serve as a reference point under clinical conditions and for other studies on the topic.</abstract><cop>Poland</cop><pub>De Gruyter</pub><pmid>34258392</pmid><doi>10.1515/med-2021-0288</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0001-6613-1642</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Age groups child fibroblast growth factors Fibroblasts Growth factors Pediatrics renal insufficiency |
title | Serum intact fibroblast growth factor 23 in healthy paediatric population |
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