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Structural analysis of human placental stem and terminal villi from normal and idiopathic growth restricted pregnancies
Studying in detail different histomorphological and pathological findings in placental stem and terminal villi of appropriate for gestational age (AGA) and idiopathic intrauterine growth restricted (IUGR) fetuses, then analyzing their correlation to the neonatal birth weight and to the some morpholo...
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Published in: | Journal of molecular histology 2012-06, Vol.43 (3), p.263-271 |
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creator | Almasry, Shaima M. Eldomiaty, Magda A. Elfayomy, Amr K. Habib, Fawzia A. Safwat, Maha D. |
description | Studying in detail different histomorphological and pathological findings in placental stem and terminal villi of appropriate for gestational age (AGA) and idiopathic intrauterine growth restricted (IUGR) fetuses, then analyzing their correlation to the neonatal birth weight and to the some morphological features of the placenta. Fifty full-term human placentae of idiopathic IUGR and 25 of AGA pregnancies were processed for haematoxylin and eosin staining and evaluated by light microscope aided with Image Analyzer. The mean number of stem villous arteries, and the mean number of terminal villous capillaries per field are significantly lower in idiopathic IUGR group (4.63 ± 0.46, 47.09 ± 4.44, respectively) than in AGA group (12.36 ± 0.61, 73.35 ± 5.13, respectively) (
p
= 0.001). Both AGA and idiopathic IUGR placentae share the presence of many pathological features: (1) narrowing of stem villous arteries appears in 38 (76 %) of IUGR cases and in 9 (36 %) of AGA cases with significant difference between groups (
p
= 0.001); (2) cellular infiltration (villitis) of the stem villi is significantly higher in IUGR cases [24 (48 %)] than in AGA cases [2 (8 %)] (
p
= 0.001). The study shows significant correlation between the birth weight and different pathologic features in the stem villi as arterial number (r = 0.494;
p
= 0.000), arterial narrowing (r = 0.283,
p
= 0.004), degenerative changes (r = 0.331,
p
= 0.001) and villitis (r = 0.275,
p
= 0.005). There is also significant correlation between neonatal birth weight and terminal villous capillary number (r = 0.281,
p
= 0.001) but no significant correlation is found between the birth weight and terminal villous fibrotic changes (r = −0.098,
p
= 0.318). Histomorphological and pathological changes in the stem villi could explore the cause of idiopathic IUGR. Stem villous arterial number, arterial narrowing, degeneration and villitis could be underlying mechanisms. Further researches on the hormonal and cytokine level should be undertaken to demonstrate the precipitating factors of these changes and the possible preventing measures. |
doi_str_mv | 10.1007/s10735-012-9405-3 |
format | article |
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p
= 0.001). Both AGA and idiopathic IUGR placentae share the presence of many pathological features: (1) narrowing of stem villous arteries appears in 38 (76 %) of IUGR cases and in 9 (36 %) of AGA cases with significant difference between groups (
p
= 0.001); (2) cellular infiltration (villitis) of the stem villi is significantly higher in IUGR cases [24 (48 %)] than in AGA cases [2 (8 %)] (
p
= 0.001). The study shows significant correlation between the birth weight and different pathologic features in the stem villi as arterial number (r = 0.494;
p
= 0.000), arterial narrowing (r = 0.283,
p
= 0.004), degenerative changes (r = 0.331,
p
= 0.001) and villitis (r = 0.275,
p
= 0.005). There is also significant correlation between neonatal birth weight and terminal villous capillary number (r = 0.281,
p
= 0.001) but no significant correlation is found between the birth weight and terminal villous fibrotic changes (r = −0.098,
p
= 0.318). Histomorphological and pathological changes in the stem villi could explore the cause of idiopathic IUGR. Stem villous arterial number, arterial narrowing, degeneration and villitis could be underlying mechanisms. Further researches on the hormonal and cytokine level should be undertaken to demonstrate the precipitating factors of these changes and the possible preventing measures.</description><identifier>ISSN: 1567-2379</identifier><identifier>EISSN: 1567-2387</identifier><identifier>DOI: 10.1007/s10735-012-9405-3</identifier><identifier>PMID: 22461195</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Adult ; Animals ; Biomedical and Life Sciences ; Biomedicine ; Birth Weight ; Capillaries - pathology ; Cell Biology ; Chorionic Villi - blood supply ; Chorionic Villi - pathology ; Developmental Biology ; Eosine Yellowish-(YS) ; Female ; Fetal Growth Retardation - pathology ; Gestational Age ; Hematoxylin ; Humans ; Immunohistochemistry ; Life Sciences ; Male ; Original Paper ; Pregnancy ; Staining and Labeling ; Umbilical Arteries - blood supply ; Umbilical Arteries - pathology</subject><ispartof>Journal of molecular histology, 2012-06, Vol.43 (3), p.263-271</ispartof><rights>Springer Science+Business Media B.V. 2012</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c438t-899cc5e5262a2baf2c0ee0f0dd1927320d3b1c14adf852ebe2025df5c8bea0e23</citedby><cites>FETCH-LOGICAL-c438t-899cc5e5262a2baf2c0ee0f0dd1927320d3b1c14adf852ebe2025df5c8bea0e23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22461195$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Almasry, Shaima M.</creatorcontrib><creatorcontrib>Eldomiaty, Magda A.</creatorcontrib><creatorcontrib>Elfayomy, Amr K.</creatorcontrib><creatorcontrib>Habib, Fawzia A.</creatorcontrib><creatorcontrib>Safwat, Maha D.</creatorcontrib><title>Structural analysis of human placental stem and terminal villi from normal and idiopathic growth restricted pregnancies</title><title>Journal of molecular histology</title><addtitle>J Mol Hist</addtitle><addtitle>J Mol Histol</addtitle><description>Studying in detail different histomorphological and pathological findings in placental stem and terminal villi of appropriate for gestational age (AGA) and idiopathic intrauterine growth restricted (IUGR) fetuses, then analyzing their correlation to the neonatal birth weight and to the some morphological features of the placenta. Fifty full-term human placentae of idiopathic IUGR and 25 of AGA pregnancies were processed for haematoxylin and eosin staining and evaluated by light microscope aided with Image Analyzer. The mean number of stem villous arteries, and the mean number of terminal villous capillaries per field are significantly lower in idiopathic IUGR group (4.63 ± 0.46, 47.09 ± 4.44, respectively) than in AGA group (12.36 ± 0.61, 73.35 ± 5.13, respectively) (
p
= 0.001). Both AGA and idiopathic IUGR placentae share the presence of many pathological features: (1) narrowing of stem villous arteries appears in 38 (76 %) of IUGR cases and in 9 (36 %) of AGA cases with significant difference between groups (
p
= 0.001); (2) cellular infiltration (villitis) of the stem villi is significantly higher in IUGR cases [24 (48 %)] than in AGA cases [2 (8 %)] (
p
= 0.001). The study shows significant correlation between the birth weight and different pathologic features in the stem villi as arterial number (r = 0.494;
p
= 0.000), arterial narrowing (r = 0.283,
p
= 0.004), degenerative changes (r = 0.331,
p
= 0.001) and villitis (r = 0.275,
p
= 0.005). There is also significant correlation between neonatal birth weight and terminal villous capillary number (r = 0.281,
p
= 0.001) but no significant correlation is found between the birth weight and terminal villous fibrotic changes (r = −0.098,
p
= 0.318). Histomorphological and pathological changes in the stem villi could explore the cause of idiopathic IUGR. Stem villous arterial number, arterial narrowing, degeneration and villitis could be underlying mechanisms. Further researches on the hormonal and cytokine level should be undertaken to demonstrate the precipitating factors of these changes and the possible preventing measures.</description><subject>Adult</subject><subject>Animals</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Birth Weight</subject><subject>Capillaries - pathology</subject><subject>Cell Biology</subject><subject>Chorionic Villi - blood supply</subject><subject>Chorionic Villi - pathology</subject><subject>Developmental Biology</subject><subject>Eosine Yellowish-(YS)</subject><subject>Female</subject><subject>Fetal Growth Retardation - pathology</subject><subject>Gestational Age</subject><subject>Hematoxylin</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Life Sciences</subject><subject>Male</subject><subject>Original Paper</subject><subject>Pregnancy</subject><subject>Staining and Labeling</subject><subject>Umbilical Arteries - blood supply</subject><subject>Umbilical Arteries - pathology</subject><issn>1567-2379</issn><issn>1567-2387</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNp1kctq3TAURUVpaB7tB3RSBJl04uboyPJjWELSBAIZpB0bWTq-V8G2XElOyN9XNzcNJdCRBGftrcdi7LOAbwKgPosCaqkKEFi0JahCvmNHQlV1gbKp37_u6_aQHcd4D4BNVbYf2CFiWQnRqiP2eJfCatIa9Mj1rMen6CL3A9-uk575MmpDc8qzmGjKgOWJwuQyyB_cODo-BD_x2YfpOW-5s84vOm2d4ZvgH9OWB4opOJPI8iXQZtazcRQ_soNBj5E-vawn7Nflxc_zq-Lm9sf1-febwpSySUXTtsYoUlihxl4PaIAIBrBWtFhLBCt7YUSp7dAopJ4QUNlBmaYnDYTyhH3d9y7B_17zVbrJRUPjqGfya-wESNx9RQUZPX2D3vs15Kc-U9CqqpRVpsSeMsHHGGjoluAmHZ4y1O2sdHsrXbbS7ax0Mme-vDSv_UT2NfFXQwZwD8Q8mjcU_j36f61_ADdwmf4</recordid><startdate>20120601</startdate><enddate>20120601</enddate><creator>Almasry, Shaima M.</creator><creator>Eldomiaty, Magda A.</creator><creator>Elfayomy, Amr K.</creator><creator>Habib, Fawzia A.</creator><creator>Safwat, Maha D.</creator><general>Springer Netherlands</general><general>Springer Nature B.V</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>7QP</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20120601</creationdate><title>Structural analysis of human placental stem and terminal villi from normal and idiopathic growth restricted pregnancies</title><author>Almasry, Shaima M. ; Eldomiaty, Magda A. ; Elfayomy, Amr K. ; Habib, Fawzia A. ; Safwat, Maha D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c438t-899cc5e5262a2baf2c0ee0f0dd1927320d3b1c14adf852ebe2025df5c8bea0e23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adult</topic><topic>Animals</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Birth Weight</topic><topic>Capillaries - pathology</topic><topic>Cell Biology</topic><topic>Chorionic Villi - blood supply</topic><topic>Chorionic Villi - pathology</topic><topic>Developmental Biology</topic><topic>Eosine Yellowish-(YS)</topic><topic>Female</topic><topic>Fetal Growth Retardation - pathology</topic><topic>Gestational Age</topic><topic>Hematoxylin</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Life Sciences</topic><topic>Male</topic><topic>Original Paper</topic><topic>Pregnancy</topic><topic>Staining and Labeling</topic><topic>Umbilical Arteries - blood supply</topic><topic>Umbilical Arteries - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Almasry, Shaima M.</creatorcontrib><creatorcontrib>Eldomiaty, Magda A.</creatorcontrib><creatorcontrib>Elfayomy, Amr K.</creatorcontrib><creatorcontrib>Habib, Fawzia A.</creatorcontrib><creatorcontrib>Safwat, Maha D.</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>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science 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>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</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><jtitle>Journal of molecular histology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Almasry, Shaima M.</au><au>Eldomiaty, Magda A.</au><au>Elfayomy, Amr K.</au><au>Habib, Fawzia A.</au><au>Safwat, Maha D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Structural analysis of human placental stem and terminal villi from normal and idiopathic growth restricted pregnancies</atitle><jtitle>Journal of molecular histology</jtitle><stitle>J Mol Hist</stitle><addtitle>J Mol Histol</addtitle><date>2012-06-01</date><risdate>2012</risdate><volume>43</volume><issue>3</issue><spage>263</spage><epage>271</epage><pages>263-271</pages><issn>1567-2379</issn><eissn>1567-2387</eissn><abstract>Studying in detail different histomorphological and pathological findings in placental stem and terminal villi of appropriate for gestational age (AGA) and idiopathic intrauterine growth restricted (IUGR) fetuses, then analyzing their correlation to the neonatal birth weight and to the some morphological features of the placenta. Fifty full-term human placentae of idiopathic IUGR and 25 of AGA pregnancies were processed for haematoxylin and eosin staining and evaluated by light microscope aided with Image Analyzer. The mean number of stem villous arteries, and the mean number of terminal villous capillaries per field are significantly lower in idiopathic IUGR group (4.63 ± 0.46, 47.09 ± 4.44, respectively) than in AGA group (12.36 ± 0.61, 73.35 ± 5.13, respectively) (
p
= 0.001). Both AGA and idiopathic IUGR placentae share the presence of many pathological features: (1) narrowing of stem villous arteries appears in 38 (76 %) of IUGR cases and in 9 (36 %) of AGA cases with significant difference between groups (
p
= 0.001); (2) cellular infiltration (villitis) of the stem villi is significantly higher in IUGR cases [24 (48 %)] than in AGA cases [2 (8 %)] (
p
= 0.001). The study shows significant correlation between the birth weight and different pathologic features in the stem villi as arterial number (r = 0.494;
p
= 0.000), arterial narrowing (r = 0.283,
p
= 0.004), degenerative changes (r = 0.331,
p
= 0.001) and villitis (r = 0.275,
p
= 0.005). There is also significant correlation between neonatal birth weight and terminal villous capillary number (r = 0.281,
p
= 0.001) but no significant correlation is found between the birth weight and terminal villous fibrotic changes (r = −0.098,
p
= 0.318). Histomorphological and pathological changes in the stem villi could explore the cause of idiopathic IUGR. Stem villous arterial number, arterial narrowing, degeneration and villitis could be underlying mechanisms. Further researches on the hormonal and cytokine level should be undertaken to demonstrate the precipitating factors of these changes and the possible preventing measures.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><pmid>22461195</pmid><doi>10.1007/s10735-012-9405-3</doi><tpages>9</tpages></addata></record> |
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subjects | Adult Animals Biomedical and Life Sciences Biomedicine Birth Weight Capillaries - pathology Cell Biology Chorionic Villi - blood supply Chorionic Villi - pathology Developmental Biology Eosine Yellowish-(YS) Female Fetal Growth Retardation - pathology Gestational Age Hematoxylin Humans Immunohistochemistry Life Sciences Male Original Paper Pregnancy Staining and Labeling Umbilical Arteries - blood supply Umbilical Arteries - pathology |
title | Structural analysis of human placental stem and terminal villi from normal and idiopathic growth restricted pregnancies |
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