Circulating microRNA expression is reduced in chronic kidney disease

Background. MicroRNAs (miRNAs) are important regulators of gene expression, which have roles in renal development and disease. They exist in biological fluids including blood and urine and may have signalling roles and potential as disease biomarkers. Methods. We measured the levels of miRNAs in pat...

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Veröffentlicht in:Nephrology, dialysis, transplantation dialysis, transplantation, 2011-11, Vol.26 (11), p.3794-3802
Hauptverfasser: Neal, Calida S., Michael, Michael Z., Pimlott, Letitia K., Yong, Tuck Y., Li, Jordan Y.Z., Gleadle, Jonathan M.
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container_end_page 3802
container_issue 11
container_start_page 3794
container_title Nephrology, dialysis, transplantation
container_volume 26
creator Neal, Calida S.
Michael, Michael Z.
Pimlott, Letitia K.
Yong, Tuck Y.
Li, Jordan Y.Z.
Gleadle, Jonathan M.
description Background. MicroRNAs (miRNAs) are important regulators of gene expression, which have roles in renal development and disease. They exist in biological fluids including blood and urine and may have signalling roles and potential as disease biomarkers. Methods. We measured the levels of miRNAs in patients with different stages of chronic kidney failure including those receiving maintenance haemodialysis treatment. Results. In patients with severe chronic renal failure, circulating levels of total and specific miRNAs are reduced in comparison to patients with mild renal impairment or normal renal function. A strong correlation exists between detected circulating miRNAs and estimated glomerular filtration rate, and less strong correlations with other features of chronic kidney disease, such as anaemia and hyperparathyroidism. Conclusion. These findings have important implications for the use of circulating miRNAs as biomarkers in individuals with renal impairment and for the pathogenesis of uraemia.
doi_str_mv 10.1093/ndt/gfr485
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MicroRNAs (miRNAs) are important regulators of gene expression, which have roles in renal development and disease. They exist in biological fluids including blood and urine and may have signalling roles and potential as disease biomarkers. Methods. We measured the levels of miRNAs in patients with different stages of chronic kidney failure including those receiving maintenance haemodialysis treatment. Results. In patients with severe chronic renal failure, circulating levels of total and specific miRNAs are reduced in comparison to patients with mild renal impairment or normal renal function. A strong correlation exists between detected circulating miRNAs and estimated glomerular filtration rate, and less strong correlations with other features of chronic kidney disease, such as anaemia and hyperparathyroidism. Conclusion. These findings have important implications for the use of circulating miRNAs as biomarkers in individuals with renal impairment and for the pathogenesis of uraemia.</description><identifier>ISSN: 0931-0509</identifier><identifier>EISSN: 1460-2385</identifier><identifier>DOI: 10.1093/ndt/gfr485</identifier><identifier>PMID: 21891774</identifier><identifier>CODEN: NDTREA</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Anemia ; Anemia - etiology ; Anemia - pathology ; Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Biological and medical sciences ; Biomarkers - analysis ; Emergency and intensive care: renal failure. Dialysis management ; Exosomes - genetics ; Female ; Follow-Up Studies ; Glomerular Filtration Rate ; Humans ; Hyperparathyroidism - etiology ; Hyperparathyroidism - pathology ; Intensive care medicine ; Kidney Failure, Chronic - genetics ; Kidney Failure, Chronic - pathology ; Kidney Failure, Chronic - surgery ; Kidney Function Tests ; Kidneys ; Male ; Medical sciences ; MicroRNAs - physiology ; Middle Aged ; Neoplastic Cells, Circulating - pathology ; Nephrology. Urinary tract diseases ; Prognosis ; Real-Time Polymerase Chain Reaction ; Renal Dialysis ; Tumors of the urinary system ; Uremia - etiology ; Uremia - pathology</subject><ispartof>Nephrology, dialysis, transplantation, 2011-11, Vol.26 (11), p.3794-3802</ispartof><rights>The Author 2011. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com 2011</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c481t-b714bfc0a6c4bf082ffe73b5a63b95c4fae31722a31fddd5b1b86aec32edecc23</citedby><cites>FETCH-LOGICAL-c481t-b714bfc0a6c4bf082ffe73b5a63b95c4fae31722a31fddd5b1b86aec32edecc23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1578,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=24740162$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21891774$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Neal, Calida S.</creatorcontrib><creatorcontrib>Michael, Michael Z.</creatorcontrib><creatorcontrib>Pimlott, Letitia K.</creatorcontrib><creatorcontrib>Yong, Tuck Y.</creatorcontrib><creatorcontrib>Li, Jordan Y.Z.</creatorcontrib><creatorcontrib>Gleadle, Jonathan M.</creatorcontrib><title>Circulating microRNA expression is reduced in chronic kidney disease</title><title>Nephrology, dialysis, transplantation</title><addtitle>Nephrol Dial Transplant</addtitle><description>Background. MicroRNAs (miRNAs) are important regulators of gene expression, which have roles in renal development and disease. They exist in biological fluids including blood and urine and may have signalling roles and potential as disease biomarkers. Methods. We measured the levels of miRNAs in patients with different stages of chronic kidney failure including those receiving maintenance haemodialysis treatment. Results. In patients with severe chronic renal failure, circulating levels of total and specific miRNAs are reduced in comparison to patients with mild renal impairment or normal renal function. A strong correlation exists between detected circulating miRNAs and estimated glomerular filtration rate, and less strong correlations with other features of chronic kidney disease, such as anaemia and hyperparathyroidism. Conclusion. These findings have important implications for the use of circulating miRNAs as biomarkers in individuals with renal impairment and for the pathogenesis of uraemia.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Anemia</subject><subject>Anemia - etiology</subject><subject>Anemia - pathology</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Biological and medical sciences</subject><subject>Biomarkers - analysis</subject><subject>Emergency and intensive care: renal failure. Dialysis management</subject><subject>Exosomes - genetics</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Glomerular Filtration Rate</subject><subject>Humans</subject><subject>Hyperparathyroidism - etiology</subject><subject>Hyperparathyroidism - pathology</subject><subject>Intensive care medicine</subject><subject>Kidney Failure, Chronic - genetics</subject><subject>Kidney Failure, Chronic - pathology</subject><subject>Kidney Failure, Chronic - surgery</subject><subject>Kidney Function Tests</subject><subject>Kidneys</subject><subject>Male</subject><subject>Medical sciences</subject><subject>MicroRNAs - physiology</subject><subject>Middle Aged</subject><subject>Neoplastic Cells, Circulating - pathology</subject><subject>Nephrology. Urinary tract diseases</subject><subject>Prognosis</subject><subject>Real-Time Polymerase Chain Reaction</subject><subject>Renal Dialysis</subject><subject>Tumors of the urinary system</subject><subject>Uremia - etiology</subject><subject>Uremia - pathology</subject><issn>0931-0509</issn><issn>1460-2385</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp90E1LwzAYwPEgipvTix9AehFFqMtL27THMV9hKIieS5o8mdE2rUkL7tsb2XS3nZ5Dfjzh-SN0SvA1wQWbWtVPl9olebqHxiTJcExZnu6jcXgkMU5xMUJH3n9gjAvK-SEaUZIXhPNkjG7mxsmhFr2xy6gx0rUvT7MIvjsH3pvWRsZHDtQgQUXGRvLdtdbI6NMoC6tIGQ_CwzE60KL2cLKZE_R2d_s6f4gXz_eP89kilklO-rjiJKm0xCKTYeKcag2cVanIWFWkMtECGOGUCka0UiqtSJVnAiSjoEBKyiboYr23c-3XAL4vG-Ml1LWw0A6-LDBh4dyMBHm5U4ZKOeN5SotAr9Y03O69A112zjTCrUqCy9--ZehbrvsGfLbZO1QNqH_6FzSA8w0QXopaO2Gl8VuX8ASTjG5dO3S7PvwBP8yRLA</recordid><startdate>20111101</startdate><enddate>20111101</enddate><creator>Neal, Calida S.</creator><creator>Michael, Michael Z.</creator><creator>Pimlott, Letitia K.</creator><creator>Yong, Tuck Y.</creator><creator>Li, Jordan Y.Z.</creator><creator>Gleadle, Jonathan M.</creator><general>Oxford University Press</general><scope>IQODW</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>7TM</scope><scope>7X8</scope></search><sort><creationdate>20111101</creationdate><title>Circulating microRNA expression is reduced in chronic kidney disease</title><author>Neal, Calida S. ; Michael, Michael Z. ; Pimlott, Letitia K. ; Yong, Tuck Y. ; Li, Jordan Y.Z. ; Gleadle, Jonathan M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c481t-b714bfc0a6c4bf082ffe73b5a63b95c4fae31722a31fddd5b1b86aec32edecc23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Anemia</topic><topic>Anemia - etiology</topic><topic>Anemia - pathology</topic><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Biological and medical sciences</topic><topic>Biomarkers - analysis</topic><topic>Emergency and intensive care: renal failure. Dialysis management</topic><topic>Exosomes - genetics</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Glomerular Filtration Rate</topic><topic>Humans</topic><topic>Hyperparathyroidism - etiology</topic><topic>Hyperparathyroidism - pathology</topic><topic>Intensive care medicine</topic><topic>Kidney Failure, Chronic - genetics</topic><topic>Kidney Failure, Chronic - pathology</topic><topic>Kidney Failure, Chronic - surgery</topic><topic>Kidney Function Tests</topic><topic>Kidneys</topic><topic>Male</topic><topic>Medical sciences</topic><topic>MicroRNAs - physiology</topic><topic>Middle Aged</topic><topic>Neoplastic Cells, Circulating - pathology</topic><topic>Nephrology. Urinary tract diseases</topic><topic>Prognosis</topic><topic>Real-Time Polymerase Chain Reaction</topic><topic>Renal Dialysis</topic><topic>Tumors of the urinary system</topic><topic>Uremia - etiology</topic><topic>Uremia - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Neal, Calida S.</creatorcontrib><creatorcontrib>Michael, Michael Z.</creatorcontrib><creatorcontrib>Pimlott, Letitia K.</creatorcontrib><creatorcontrib>Yong, Tuck Y.</creatorcontrib><creatorcontrib>Li, Jordan Y.Z.</creatorcontrib><creatorcontrib>Gleadle, Jonathan M.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Nephrology, dialysis, transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Neal, Calida S.</au><au>Michael, Michael Z.</au><au>Pimlott, Letitia K.</au><au>Yong, Tuck Y.</au><au>Li, Jordan Y.Z.</au><au>Gleadle, Jonathan M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Circulating microRNA expression is reduced in chronic kidney disease</atitle><jtitle>Nephrology, dialysis, transplantation</jtitle><addtitle>Nephrol Dial Transplant</addtitle><date>2011-11-01</date><risdate>2011</risdate><volume>26</volume><issue>11</issue><spage>3794</spage><epage>3802</epage><pages>3794-3802</pages><issn>0931-0509</issn><eissn>1460-2385</eissn><coden>NDTREA</coden><abstract>Background. MicroRNAs (miRNAs) are important regulators of gene expression, which have roles in renal development and disease. They exist in biological fluids including blood and urine and may have signalling roles and potential as disease biomarkers. Methods. We measured the levels of miRNAs in patients with different stages of chronic kidney failure including those receiving maintenance haemodialysis treatment. Results. In patients with severe chronic renal failure, circulating levels of total and specific miRNAs are reduced in comparison to patients with mild renal impairment or normal renal function. A strong correlation exists between detected circulating miRNAs and estimated glomerular filtration rate, and less strong correlations with other features of chronic kidney disease, such as anaemia and hyperparathyroidism. Conclusion. 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source Oxford University Press Journals All Titles (1996-Current); MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection
subjects Adult
Aged
Aged, 80 and over
Anemia
Anemia - etiology
Anemia - pathology
Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
Biological and medical sciences
Biomarkers - analysis
Emergency and intensive care: renal failure. Dialysis management
Exosomes - genetics
Female
Follow-Up Studies
Glomerular Filtration Rate
Humans
Hyperparathyroidism - etiology
Hyperparathyroidism - pathology
Intensive care medicine
Kidney Failure, Chronic - genetics
Kidney Failure, Chronic - pathology
Kidney Failure, Chronic - surgery
Kidney Function Tests
Kidneys
Male
Medical sciences
MicroRNAs - physiology
Middle Aged
Neoplastic Cells, Circulating - pathology
Nephrology. Urinary tract diseases
Prognosis
Real-Time Polymerase Chain Reaction
Renal Dialysis
Tumors of the urinary system
Uremia - etiology
Uremia - pathology
title Circulating microRNA expression is reduced in chronic kidney disease
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