Can measurement of the foetal renal parenchymal thickness with ultrasound be used as an indirect measure of nephron number?
Chronic kidney disease continues to be under recognised and is associated with a significant global health burden and costs. An adverse intrauterine environment may result in a depleted nephron number and an increased risk of chronic kidney disease. Antenatal ultrasound was used to measure the foeta...
Gespeichert in:
Veröffentlicht in: | Journal of developmental origins of health and disease 2021-04, Vol.12 (2), p.184-192 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 192 |
---|---|
container_issue | 2 |
container_start_page | 184 |
container_title | Journal of developmental origins of health and disease |
container_volume | 12 |
creator | Brennan, Sonja Watson, David Schneider, Michal Rudd, Donna Kandasamy, Yogavijayan |
description | Chronic kidney disease continues to be under recognised and is associated with a significant global health burden and costs. An adverse intrauterine environment may result in a depleted nephron number and an increased risk of chronic kidney disease. Antenatal ultrasound was used to measure the foetal renal parenchymal thickness (RPT), as a novel method to estimate nephron number. Foetal renal artery blood flow was also assessed. This prospective, longitudinal study evaluated the foetal kidneys of 102 appropriately grown and 30 foetal growth-restricted foetuses between 20 and 37 weeks gestational age (GA) to provide vital knowledge on the influences foetal growth restriction has on the developing kidneys. The foetal RPT and renal artery blood flow were measured at least every 4 weeks using ultrasound. The RPT was found to be significantly thinner in growth-restricted foetuses compared to appropriately grown foetuses [likelihood ratio (LR) = 21.06, P ≤ 0.0001] and the difference increases with GA. In foetuses with the same head circumference, a growth-restricted foetus was more likely to have a thinner parenchyma than an appropriately grown foetus (LR = 8.9, P = 0.0028), supporting the principle that growth-restricted foetuses preferentially shunt blood towards the brain. No significant difference was seen in the renal arteries between appropriately grown and growth-restricted foetuses. Measurement of the RPT appears to be a more sensitive measure than current methods. It has the potential to identify infants with a possible reduced nephron endowment allowing for monitoring and interventions to be focused on individuals at a higher risk of developing future hypertension and chronic kidney disease. |
doi_str_mv | 10.1017/S204017442000015X |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2503606581</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><cupid>10_1017_S204017442000015X</cupid><sourcerecordid>2503606581</sourcerecordid><originalsourceid>FETCH-LOGICAL-c373t-11c5569756937526617dab3e2c319e19f5b08c4cefbf79294b9c71477e2916e93</originalsourceid><addsrcrecordid>eNp1kE9LAzEQxYMoVqofwIsEPFczSXbTnESK_6DgQQVvSzY76652szXJIsUvb4qtHsRA8obw3m-YIeQY2BkwUOcPnMmkUnKWDmTPO-Rg_TUBlfHdn1rKETkK4XVtEiBTZJ-MBOeaTTUckM-ZcbRDEwaPHbpI-5rGBmndYzQL6tGld2mS2mbVpTo2rX1zGAL9aGNDh0X0JvSDq2iJdAhYURNoYrauaj3auIWvwQ6Xje8ddUNXor84JHu1WQQ82uiYPF1fPc5uJ_P7m7vZ5XxihRJxAmCzLNcqXZFGy3NQlSkFcitAI-g6K9nUSot1WSvNtSy1VSCVQq4hRy3G5PSbu_T9-4AhFq_94NNgoeAZEznLsykkF3y7rO9D8FgXS992xq8KYMV648WfjafMyYY8lB1WP4ntfpNBbKCmK31bveBv7_-xX_OnisY</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2503606581</pqid></control><display><type>article</type><title>Can measurement of the foetal renal parenchymal thickness with ultrasound be used as an indirect measure of nephron number?</title><source>MEDLINE</source><source>Cambridge Journals</source><creator>Brennan, Sonja ; Watson, David ; Schneider, Michal ; Rudd, Donna ; Kandasamy, Yogavijayan</creator><creatorcontrib>Brennan, Sonja ; Watson, David ; Schneider, Michal ; Rudd, Donna ; Kandasamy, Yogavijayan</creatorcontrib><description>Chronic kidney disease continues to be under recognised and is associated with a significant global health burden and costs. An adverse intrauterine environment may result in a depleted nephron number and an increased risk of chronic kidney disease. Antenatal ultrasound was used to measure the foetal renal parenchymal thickness (RPT), as a novel method to estimate nephron number. Foetal renal artery blood flow was also assessed. This prospective, longitudinal study evaluated the foetal kidneys of 102 appropriately grown and 30 foetal growth-restricted foetuses between 20 and 37 weeks gestational age (GA) to provide vital knowledge on the influences foetal growth restriction has on the developing kidneys. The foetal RPT and renal artery blood flow were measured at least every 4 weeks using ultrasound. The RPT was found to be significantly thinner in growth-restricted foetuses compared to appropriately grown foetuses [likelihood ratio (LR) = 21.06, P ≤ 0.0001] and the difference increases with GA. In foetuses with the same head circumference, a growth-restricted foetus was more likely to have a thinner parenchyma than an appropriately grown foetus (LR = 8.9, P = 0.0028), supporting the principle that growth-restricted foetuses preferentially shunt blood towards the brain. No significant difference was seen in the renal arteries between appropriately grown and growth-restricted foetuses. Measurement of the RPT appears to be a more sensitive measure than current methods. It has the potential to identify infants with a possible reduced nephron endowment allowing for monitoring and interventions to be focused on individuals at a higher risk of developing future hypertension and chronic kidney disease.</description><identifier>ISSN: 2040-1744</identifier><identifier>EISSN: 2040-1752</identifier><identifier>DOI: 10.1017/S204017442000015X</identifier><identifier>PMID: 32290891</identifier><language>eng</language><publisher>Cambridge, UK: Cambridge University Press</publisher><subject>Adult ; Birth weight ; Chronic illnesses ; Female ; Fetal Growth Retardation - diagnosis ; Fetal Growth Retardation - diagnostic imaging ; Fetus - diagnostic imaging ; Fetus - pathology ; Gestational Age ; Hospitals ; Humans ; Hypertension ; Infant, Newborn ; Kidney - diagnostic imaging ; Kidney - pathology ; Kidney diseases ; Longitudinal Studies ; Male ; Nephrons - diagnostic imaging ; Nephrons - pathology ; Obstetrics ; Original Article ; Pregnancy ; Prenatal Care ; Prospective Studies ; Sinuses ; Ultrasonic imaging ; Ultrasonography, Prenatal - methods ; Veins & arteries ; Womens health</subject><ispartof>Journal of developmental origins of health and disease, 2021-04, Vol.12 (2), p.184-192</ispartof><rights>Cambridge University Press and the International Society for Developmental Origins of Health and Disease 2020</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c373t-11c5569756937526617dab3e2c319e19f5b08c4cefbf79294b9c71477e2916e93</citedby><cites>FETCH-LOGICAL-c373t-11c5569756937526617dab3e2c319e19f5b08c4cefbf79294b9c71477e2916e93</cites><orcidid>0000-0002-7634-9546</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.cambridge.org/core/product/identifier/S204017442000015X/type/journal_article$$EHTML$$P50$$Gcambridge$$H</linktohtml><link.rule.ids>164,315,781,785,27926,27927,55630</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32290891$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Brennan, Sonja</creatorcontrib><creatorcontrib>Watson, David</creatorcontrib><creatorcontrib>Schneider, Michal</creatorcontrib><creatorcontrib>Rudd, Donna</creatorcontrib><creatorcontrib>Kandasamy, Yogavijayan</creatorcontrib><title>Can measurement of the foetal renal parenchymal thickness with ultrasound be used as an indirect measure of nephron number?</title><title>Journal of developmental origins of health and disease</title><addtitle>J Dev Orig Health Dis</addtitle><description>Chronic kidney disease continues to be under recognised and is associated with a significant global health burden and costs. An adverse intrauterine environment may result in a depleted nephron number and an increased risk of chronic kidney disease. Antenatal ultrasound was used to measure the foetal renal parenchymal thickness (RPT), as a novel method to estimate nephron number. Foetal renal artery blood flow was also assessed. This prospective, longitudinal study evaluated the foetal kidneys of 102 appropriately grown and 30 foetal growth-restricted foetuses between 20 and 37 weeks gestational age (GA) to provide vital knowledge on the influences foetal growth restriction has on the developing kidneys. The foetal RPT and renal artery blood flow were measured at least every 4 weeks using ultrasound. The RPT was found to be significantly thinner in growth-restricted foetuses compared to appropriately grown foetuses [likelihood ratio (LR) = 21.06, P ≤ 0.0001] and the difference increases with GA. In foetuses with the same head circumference, a growth-restricted foetus was more likely to have a thinner parenchyma than an appropriately grown foetus (LR = 8.9, P = 0.0028), supporting the principle that growth-restricted foetuses preferentially shunt blood towards the brain. No significant difference was seen in the renal arteries between appropriately grown and growth-restricted foetuses. Measurement of the RPT appears to be a more sensitive measure than current methods. It has the potential to identify infants with a possible reduced nephron endowment allowing for monitoring and interventions to be focused on individuals at a higher risk of developing future hypertension and chronic kidney disease.</description><subject>Adult</subject><subject>Birth weight</subject><subject>Chronic illnesses</subject><subject>Female</subject><subject>Fetal Growth Retardation - diagnosis</subject><subject>Fetal Growth Retardation - diagnostic imaging</subject><subject>Fetus - diagnostic imaging</subject><subject>Fetus - pathology</subject><subject>Gestational Age</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Hypertension</subject><subject>Infant, Newborn</subject><subject>Kidney - diagnostic imaging</subject><subject>Kidney - pathology</subject><subject>Kidney diseases</subject><subject>Longitudinal Studies</subject><subject>Male</subject><subject>Nephrons - diagnostic imaging</subject><subject>Nephrons - pathology</subject><subject>Obstetrics</subject><subject>Original Article</subject><subject>Pregnancy</subject><subject>Prenatal Care</subject><subject>Prospective Studies</subject><subject>Sinuses</subject><subject>Ultrasonic imaging</subject><subject>Ultrasonography, Prenatal - methods</subject><subject>Veins & arteries</subject><subject>Womens health</subject><issn>2040-1744</issn><issn>2040-1752</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp1kE9LAzEQxYMoVqofwIsEPFczSXbTnESK_6DgQQVvSzY76652szXJIsUvb4qtHsRA8obw3m-YIeQY2BkwUOcPnMmkUnKWDmTPO-Rg_TUBlfHdn1rKETkK4XVtEiBTZJ-MBOeaTTUckM-ZcbRDEwaPHbpI-5rGBmndYzQL6tGld2mS2mbVpTo2rX1zGAL9aGNDh0X0JvSDq2iJdAhYURNoYrauaj3auIWvwQ6Xje8ddUNXor84JHu1WQQ82uiYPF1fPc5uJ_P7m7vZ5XxihRJxAmCzLNcqXZFGy3NQlSkFcitAI-g6K9nUSot1WSvNtSy1VSCVQq4hRy3G5PSbu_T9-4AhFq_94NNgoeAZEznLsykkF3y7rO9D8FgXS992xq8KYMV648WfjafMyYY8lB1WP4ntfpNBbKCmK31bveBv7_-xX_OnisY</recordid><startdate>202104</startdate><enddate>202104</enddate><creator>Brennan, Sonja</creator><creator>Watson, David</creator><creator>Schneider, Michal</creator><creator>Rudd, Donna</creator><creator>Kandasamy, Yogavijayan</creator><general>Cambridge University Press</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>3V.</scope><scope>7X7</scope><scope>7XB</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><orcidid>https://orcid.org/0000-0002-7634-9546</orcidid></search><sort><creationdate>202104</creationdate><title>Can measurement of the foetal renal parenchymal thickness with ultrasound be used as an indirect measure of nephron number?</title><author>Brennan, Sonja ; Watson, David ; Schneider, Michal ; Rudd, Donna ; Kandasamy, Yogavijayan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c373t-11c5569756937526617dab3e2c319e19f5b08c4cefbf79294b9c71477e2916e93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adult</topic><topic>Birth weight</topic><topic>Chronic illnesses</topic><topic>Female</topic><topic>Fetal Growth Retardation - diagnosis</topic><topic>Fetal Growth Retardation - diagnostic imaging</topic><topic>Fetus - diagnostic imaging</topic><topic>Fetus - pathology</topic><topic>Gestational Age</topic><topic>Hospitals</topic><topic>Humans</topic><topic>Hypertension</topic><topic>Infant, Newborn</topic><topic>Kidney - diagnostic imaging</topic><topic>Kidney - pathology</topic><topic>Kidney diseases</topic><topic>Longitudinal Studies</topic><topic>Male</topic><topic>Nephrons - diagnostic imaging</topic><topic>Nephrons - pathology</topic><topic>Obstetrics</topic><topic>Original Article</topic><topic>Pregnancy</topic><topic>Prenatal Care</topic><topic>Prospective Studies</topic><topic>Sinuses</topic><topic>Ultrasonic imaging</topic><topic>Ultrasonography, Prenatal - methods</topic><topic>Veins & arteries</topic><topic>Womens health</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Brennan, Sonja</creatorcontrib><creatorcontrib>Watson, David</creatorcontrib><creatorcontrib>Schneider, Michal</creatorcontrib><creatorcontrib>Rudd, Donna</creatorcontrib><creatorcontrib>Kandasamy, Yogavijayan</creatorcontrib><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>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</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 Central UK/Ireland</collection><collection>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><jtitle>Journal of developmental origins of health and disease</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Brennan, Sonja</au><au>Watson, David</au><au>Schneider, Michal</au><au>Rudd, Donna</au><au>Kandasamy, Yogavijayan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Can measurement of the foetal renal parenchymal thickness with ultrasound be used as an indirect measure of nephron number?</atitle><jtitle>Journal of developmental origins of health and disease</jtitle><addtitle>J Dev Orig Health Dis</addtitle><date>2021-04</date><risdate>2021</risdate><volume>12</volume><issue>2</issue><spage>184</spage><epage>192</epage><pages>184-192</pages><issn>2040-1744</issn><eissn>2040-1752</eissn><abstract>Chronic kidney disease continues to be under recognised and is associated with a significant global health burden and costs. An adverse intrauterine environment may result in a depleted nephron number and an increased risk of chronic kidney disease. Antenatal ultrasound was used to measure the foetal renal parenchymal thickness (RPT), as a novel method to estimate nephron number. Foetal renal artery blood flow was also assessed. This prospective, longitudinal study evaluated the foetal kidneys of 102 appropriately grown and 30 foetal growth-restricted foetuses between 20 and 37 weeks gestational age (GA) to provide vital knowledge on the influences foetal growth restriction has on the developing kidneys. The foetal RPT and renal artery blood flow were measured at least every 4 weeks using ultrasound. The RPT was found to be significantly thinner in growth-restricted foetuses compared to appropriately grown foetuses [likelihood ratio (LR) = 21.06, P ≤ 0.0001] and the difference increases with GA. In foetuses with the same head circumference, a growth-restricted foetus was more likely to have a thinner parenchyma than an appropriately grown foetus (LR = 8.9, P = 0.0028), supporting the principle that growth-restricted foetuses preferentially shunt blood towards the brain. No significant difference was seen in the renal arteries between appropriately grown and growth-restricted foetuses. Measurement of the RPT appears to be a more sensitive measure than current methods. It has the potential to identify infants with a possible reduced nephron endowment allowing for monitoring and interventions to be focused on individuals at a higher risk of developing future hypertension and chronic kidney disease.</abstract><cop>Cambridge, UK</cop><pub>Cambridge University Press</pub><pmid>32290891</pmid><doi>10.1017/S204017442000015X</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-7634-9546</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2040-1744 |
ispartof | Journal of developmental origins of health and disease, 2021-04, Vol.12 (2), p.184-192 |
issn | 2040-1744 2040-1752 |
language | eng |
recordid | cdi_proquest_journals_2503606581 |
source | MEDLINE; Cambridge Journals |
subjects | Adult Birth weight Chronic illnesses Female Fetal Growth Retardation - diagnosis Fetal Growth Retardation - diagnostic imaging Fetus - diagnostic imaging Fetus - pathology Gestational Age Hospitals Humans Hypertension Infant, Newborn Kidney - diagnostic imaging Kidney - pathology Kidney diseases Longitudinal Studies Male Nephrons - diagnostic imaging Nephrons - pathology Obstetrics Original Article Pregnancy Prenatal Care Prospective Studies Sinuses Ultrasonic imaging Ultrasonography, Prenatal - methods Veins & arteries Womens health |
title | Can measurement of the foetal renal parenchymal thickness with ultrasound be used as an indirect measure of nephron number? |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-18T05%3A29%3A04IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Can%20measurement%20of%20the%20foetal%20renal%20parenchymal%20thickness%20with%20ultrasound%20be%20used%20as%20an%20indirect%20measure%20of%20nephron%20number?&rft.jtitle=Journal%20of%20developmental%20origins%20of%20health%20and%20disease&rft.au=Brennan,%20Sonja&rft.date=2021-04&rft.volume=12&rft.issue=2&rft.spage=184&rft.epage=192&rft.pages=184-192&rft.issn=2040-1744&rft.eissn=2040-1752&rft_id=info:doi/10.1017/S204017442000015X&rft_dat=%3Cproquest_cross%3E2503606581%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2503606581&rft_id=info:pmid/32290891&rft_cupid=10_1017_S204017442000015X&rfr_iscdi=true |