Evaluation of Renal Glomerular and Tubular Functional and Structural Integrity in Neonates
Renal cells are not fully differentiated at birth, representing a major risk in preterm infants. We evaluated glomerular and tubular functional integrity as well as structural integrity of renal tubules among healthy full-term and preterm infants as well as diseased preterm infants. A total of 50 ne...
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Veröffentlicht in: | The American journal of the medical sciences 2002-11, Vol.324 (5), p.261-266 |
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description | Renal cells are not fully differentiated at birth, representing a major risk in preterm infants. We evaluated glomerular and tubular functional integrity as well as structural integrity of renal tubules among healthy full-term and preterm infants as well as diseased preterm infants.
A total of 50 newborns (10 healthy full-term, 10 healthy preterm, and 30 diseased preterm, at 38.9 ± 1.10, 34.2 ± 0.92, and 32 ± 2.47 weeks gestational age, respectively) were included in the present study. Glomerular function was assessed by measuring urinary levels of both microalbumin and immunoglobulin G as well as serum creatinine levels, whereas the proximal tubular function was investigated by measuring the urinary levels of both α1-microglobulin and β2-microglobulin as well as retinol-binding protein. Also, distal tubular reabsorption capacity was investigated by assessing fractional excretion of sodium. Moreover, the structural integrity of renal proximal tubules was studied by measuring the urinary activities of both the brush-border membrane enzyme leucine-aminopeptidase (LAP) and the lysosomal enzyme N-acetyl-β-d-glucosaminidase. The preceding investigations were done on both the first and third days of life of all 50 newborns.
Glomerular and tubular function and structure was relatively impaired at birth among both healthy and diseased preterm as well as healthy full-term neonates and improved rapidly thereafter. The diseased preterm neonates showed worse renal function and structure with minimal improvement regardless of the underlying sickness.
Renal insufficiency and renal immaturity could be evaluated using enzymuria and low- and high-molecular-weight proteinuria as noninvasive methods. |
doi_str_mv | 10.1097/00000441-200211000-00005 |
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A total of 50 newborns (10 healthy full-term, 10 healthy preterm, and 30 diseased preterm, at 38.9 ± 1.10, 34.2 ± 0.92, and 32 ± 2.47 weeks gestational age, respectively) were included in the present study. Glomerular function was assessed by measuring urinary levels of both microalbumin and immunoglobulin G as well as serum creatinine levels, whereas the proximal tubular function was investigated by measuring the urinary levels of both α1-microglobulin and β2-microglobulin as well as retinol-binding protein. Also, distal tubular reabsorption capacity was investigated by assessing fractional excretion of sodium. Moreover, the structural integrity of renal proximal tubules was studied by measuring the urinary activities of both the brush-border membrane enzyme leucine-aminopeptidase (LAP) and the lysosomal enzyme N-acetyl-β-d-glucosaminidase. The preceding investigations were done on both the first and third days of life of all 50 newborns.
Glomerular and tubular function and structure was relatively impaired at birth among both healthy and diseased preterm as well as healthy full-term neonates and improved rapidly thereafter. The diseased preterm neonates showed worse renal function and structure with minimal improvement regardless of the underlying sickness.
Renal insufficiency and renal immaturity could be evaluated using enzymuria and low- and high-molecular-weight proteinuria as noninvasive methods.</description><identifier>ISSN: 0002-9629</identifier><identifier>EISSN: 1538-2990</identifier><identifier>DOI: 10.1097/00000441-200211000-00005</identifier><identifier>PMID: 12449447</identifier><identifier>CODEN: AJMSA9</identifier><language>eng</language><publisher>Hagerstown, MD: Elsevier Inc</publisher><subject>Albumins - analysis ; Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Biological and medical sciences ; Cell Differentiation ; Creatinine - blood ; Emergency and intensive care: renal failure. Dialysis management ; Enzymes - urine ; Enzymuria ; Fetal Organ Maturity - physiology ; Gestational Age ; Glomerular and tubular integrity ; High- and low-molecular-weight proteinuria ; Humans ; Immunoglobulin G - urine ; Infant, Newborn ; Infant, Premature ; Intensive care medicine ; Kidney - cytology ; Kidney - physiology ; Kidney - physiopathology ; Kidney Function Tests - statistics & numerical data ; Kidney Glomerulus - physiology ; Kidney Glomerulus - physiopathology ; Kidney Tubules, Distal - physiology ; Kidney Tubules, Distal - physiopathology ; Kidney Tubules, Proximal - physiology ; Kidney Tubules, Proximal - physiopathology ; Medical sciences ; Membrane Glycoproteins - urine ; Predictive Value of Tests ; Reference Values ; Renal immaturity ; Renal Insufficiency - diagnosis ; Renal Insufficiency - physiopathology ; Renal Insufficiency - urine ; Retinol-Binding Proteins - urine ; Sodium - urine ; Trypsin Inhibitor, Kunitz Soybean ; Urinalysis - statistics & numerical data</subject><ispartof>The American journal of the medical sciences, 2002-11, Vol.324 (5), p.261-266</ispartof><rights>2002 Southern Society for Clinical Investigation</rights><rights>2003 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c400t-20492a641bf3099c5fd3df565c9ad5f359967ccb2924a1e0413ad1cb3eef62023</citedby><cites>FETCH-LOGICAL-c400t-20492a641bf3099c5fd3df565c9ad5f359967ccb2924a1e0413ad1cb3eef62023</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14023640$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12449447$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Awad, Hesham</creatorcontrib><creatorcontrib>El-Barbary, Mohamed</creatorcontrib><creatorcontrib>Imam, Safaa</creatorcontrib><creatorcontrib>El-Safty, Ibrahim</creatorcontrib><title>Evaluation of Renal Glomerular and Tubular Functional and Structural Integrity in Neonates</title><title>The American journal of the medical sciences</title><addtitle>Am J Med Sci</addtitle><description>Renal cells are not fully differentiated at birth, representing a major risk in preterm infants. We evaluated glomerular and tubular functional integrity as well as structural integrity of renal tubules among healthy full-term and preterm infants as well as diseased preterm infants.
A total of 50 newborns (10 healthy full-term, 10 healthy preterm, and 30 diseased preterm, at 38.9 ± 1.10, 34.2 ± 0.92, and 32 ± 2.47 weeks gestational age, respectively) were included in the present study. Glomerular function was assessed by measuring urinary levels of both microalbumin and immunoglobulin G as well as serum creatinine levels, whereas the proximal tubular function was investigated by measuring the urinary levels of both α1-microglobulin and β2-microglobulin as well as retinol-binding protein. Also, distal tubular reabsorption capacity was investigated by assessing fractional excretion of sodium. Moreover, the structural integrity of renal proximal tubules was studied by measuring the urinary activities of both the brush-border membrane enzyme leucine-aminopeptidase (LAP) and the lysosomal enzyme N-acetyl-β-d-glucosaminidase. The preceding investigations were done on both the first and third days of life of all 50 newborns.
Glomerular and tubular function and structure was relatively impaired at birth among both healthy and diseased preterm as well as healthy full-term neonates and improved rapidly thereafter. The diseased preterm neonates showed worse renal function and structure with minimal improvement regardless of the underlying sickness.
Renal insufficiency and renal immaturity could be evaluated using enzymuria and low- and high-molecular-weight proteinuria as noninvasive methods.</description><subject>Albumins - analysis</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Biological and medical sciences</subject><subject>Cell Differentiation</subject><subject>Creatinine - blood</subject><subject>Emergency and intensive care: renal failure. Dialysis management</subject><subject>Enzymes - urine</subject><subject>Enzymuria</subject><subject>Fetal Organ Maturity - physiology</subject><subject>Gestational Age</subject><subject>Glomerular and tubular integrity</subject><subject>High- and low-molecular-weight proteinuria</subject><subject>Humans</subject><subject>Immunoglobulin G - urine</subject><subject>Infant, Newborn</subject><subject>Infant, Premature</subject><subject>Intensive care medicine</subject><subject>Kidney - cytology</subject><subject>Kidney - physiology</subject><subject>Kidney - physiopathology</subject><subject>Kidney Function Tests - statistics & numerical data</subject><subject>Kidney Glomerulus - physiology</subject><subject>Kidney Glomerulus - physiopathology</subject><subject>Kidney Tubules, Distal - physiology</subject><subject>Kidney Tubules, Distal - physiopathology</subject><subject>Kidney Tubules, Proximal - physiology</subject><subject>Kidney Tubules, Proximal - physiopathology</subject><subject>Medical sciences</subject><subject>Membrane Glycoproteins - urine</subject><subject>Predictive Value of Tests</subject><subject>Reference Values</subject><subject>Renal immaturity</subject><subject>Renal Insufficiency - diagnosis</subject><subject>Renal Insufficiency - physiopathology</subject><subject>Renal Insufficiency - urine</subject><subject>Retinol-Binding Proteins - urine</subject><subject>Sodium - urine</subject><subject>Trypsin Inhibitor, Kunitz Soybean</subject><subject>Urinalysis - statistics & numerical data</subject><issn>0002-9629</issn><issn>1538-2990</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMtOAyEUhonRaL28gpmN7kaBYWbKUk1bmzSaeNm4IQxzMJgpU7k08e1lbLVL2cD58x04fAhlBF8RzOtrPCzGSE4xpoSkIh-Scg-NSFmMc8o53kejFNGcV5QfoWPvPzAmdEyKQ3REKGOcsXqE3iZr2UUZTG-zXmdPYGWXzbp-CS520mXSttlLbH7O02jVACZiiJ-DiypEl8q5DfDuTPjKjM0eICEB_Ck60LLzcLbdT9DrdPJyd58vHmfzu5tFrhjGIX2BcSorRhpdYM5Vqdui1WVVKi7bUhcl51WtVEM5ZZIAZqSQLVFNAaArimlxgi43965c_xnBB7E0XkHXSQt99KKmNUkSBnC8AZXrvXegxcqZpXRfgmAxeBW_XsWf15-oTK3n2zdis4R217gVmYCLLSC9kp120irjdxxLg1YMJ-52w0EysjbghFcGrILWOFBBtL35f5pvor2UFA</recordid><startdate>20021101</startdate><enddate>20021101</enddate><creator>Awad, Hesham</creator><creator>El-Barbary, Mohamed</creator><creator>Imam, Safaa</creator><creator>El-Safty, Ibrahim</creator><general>Elsevier Inc</general><general>Lippincott</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>7X8</scope></search><sort><creationdate>20021101</creationdate><title>Evaluation of Renal Glomerular and Tubular Functional and Structural Integrity in Neonates</title><author>Awad, Hesham ; El-Barbary, Mohamed ; Imam, Safaa ; El-Safty, Ibrahim</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c400t-20492a641bf3099c5fd3df565c9ad5f359967ccb2924a1e0413ad1cb3eef62023</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Albumins - analysis</topic><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Biological and medical sciences</topic><topic>Cell Differentiation</topic><topic>Creatinine - blood</topic><topic>Emergency and intensive care: renal failure. Dialysis management</topic><topic>Enzymes - urine</topic><topic>Enzymuria</topic><topic>Fetal Organ Maturity - physiology</topic><topic>Gestational Age</topic><topic>Glomerular and tubular integrity</topic><topic>High- and low-molecular-weight proteinuria</topic><topic>Humans</topic><topic>Immunoglobulin G - urine</topic><topic>Infant, Newborn</topic><topic>Infant, Premature</topic><topic>Intensive care medicine</topic><topic>Kidney - cytology</topic><topic>Kidney - physiology</topic><topic>Kidney - physiopathology</topic><topic>Kidney Function Tests - statistics & numerical data</topic><topic>Kidney Glomerulus - physiology</topic><topic>Kidney Glomerulus - physiopathology</topic><topic>Kidney Tubules, Distal - physiology</topic><topic>Kidney Tubules, Distal - physiopathology</topic><topic>Kidney Tubules, Proximal - physiology</topic><topic>Kidney Tubules, Proximal - physiopathology</topic><topic>Medical sciences</topic><topic>Membrane Glycoproteins - urine</topic><topic>Predictive Value of Tests</topic><topic>Reference Values</topic><topic>Renal immaturity</topic><topic>Renal Insufficiency - diagnosis</topic><topic>Renal Insufficiency - physiopathology</topic><topic>Renal Insufficiency - urine</topic><topic>Retinol-Binding Proteins - urine</topic><topic>Sodium - urine</topic><topic>Trypsin Inhibitor, Kunitz Soybean</topic><topic>Urinalysis - statistics & numerical data</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Awad, Hesham</creatorcontrib><creatorcontrib>El-Barbary, Mohamed</creatorcontrib><creatorcontrib>Imam, Safaa</creatorcontrib><creatorcontrib>El-Safty, Ibrahim</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>MEDLINE - Academic</collection><jtitle>The American journal of the medical sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Awad, Hesham</au><au>El-Barbary, Mohamed</au><au>Imam, Safaa</au><au>El-Safty, Ibrahim</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of Renal Glomerular and Tubular Functional and Structural Integrity in Neonates</atitle><jtitle>The American journal of the medical sciences</jtitle><addtitle>Am J Med Sci</addtitle><date>2002-11-01</date><risdate>2002</risdate><volume>324</volume><issue>5</issue><spage>261</spage><epage>266</epage><pages>261-266</pages><issn>0002-9629</issn><eissn>1538-2990</eissn><coden>AJMSA9</coden><abstract>Renal cells are not fully differentiated at birth, representing a major risk in preterm infants. We evaluated glomerular and tubular functional integrity as well as structural integrity of renal tubules among healthy full-term and preterm infants as well as diseased preterm infants.
A total of 50 newborns (10 healthy full-term, 10 healthy preterm, and 30 diseased preterm, at 38.9 ± 1.10, 34.2 ± 0.92, and 32 ± 2.47 weeks gestational age, respectively) were included in the present study. Glomerular function was assessed by measuring urinary levels of both microalbumin and immunoglobulin G as well as serum creatinine levels, whereas the proximal tubular function was investigated by measuring the urinary levels of both α1-microglobulin and β2-microglobulin as well as retinol-binding protein. Also, distal tubular reabsorption capacity was investigated by assessing fractional excretion of sodium. Moreover, the structural integrity of renal proximal tubules was studied by measuring the urinary activities of both the brush-border membrane enzyme leucine-aminopeptidase (LAP) and the lysosomal enzyme N-acetyl-β-d-glucosaminidase. The preceding investigations were done on both the first and third days of life of all 50 newborns.
Glomerular and tubular function and structure was relatively impaired at birth among both healthy and diseased preterm as well as healthy full-term neonates and improved rapidly thereafter. The diseased preterm neonates showed worse renal function and structure with minimal improvement regardless of the underlying sickness.
Renal insufficiency and renal immaturity could be evaluated using enzymuria and low- and high-molecular-weight proteinuria as noninvasive methods.</abstract><cop>Hagerstown, MD</cop><pub>Elsevier Inc</pub><pmid>12449447</pmid><doi>10.1097/00000441-200211000-00005</doi><tpages>6</tpages></addata></record> |
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subjects | Albumins - analysis Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Biological and medical sciences Cell Differentiation Creatinine - blood Emergency and intensive care: renal failure. Dialysis management Enzymes - urine Enzymuria Fetal Organ Maturity - physiology Gestational Age Glomerular and tubular integrity High- and low-molecular-weight proteinuria Humans Immunoglobulin G - urine Infant, Newborn Infant, Premature Intensive care medicine Kidney - cytology Kidney - physiology Kidney - physiopathology Kidney Function Tests - statistics & numerical data Kidney Glomerulus - physiology Kidney Glomerulus - physiopathology Kidney Tubules, Distal - physiology Kidney Tubules, Distal - physiopathology Kidney Tubules, Proximal - physiology Kidney Tubules, Proximal - physiopathology Medical sciences Membrane Glycoproteins - urine Predictive Value of Tests Reference Values Renal immaturity Renal Insufficiency - diagnosis Renal Insufficiency - physiopathology Renal Insufficiency - urine Retinol-Binding Proteins - urine Sodium - urine Trypsin Inhibitor, Kunitz Soybean Urinalysis - statistics & numerical data |
title | Evaluation of Renal Glomerular and Tubular Functional and Structural Integrity in Neonates |
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