{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,29]],"date-time":"2026-09-29T03:55:35Z","timestamp":1790654135870,"version":"4.1.0"},"reference-count":62,"publisher":"Wiley","issue":"6","license":[{"start":{"date-parts":[[2025,5,7]],"date-time":"2025-05-07T00:00:00Z","timestamp":1746576000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"},{"start":{"date-parts":[[2025,5,7]],"date-time":"2025-05-07T00:00:00Z","timestamp":1746576000000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"funder":[{"DOI":"10.13039\/100015471","name":"Mater Foundation","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100015471","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100000925","name":"National Health and Medical Research Council","doi-asserted-by":"publisher","id":[{"id":"10.13039\/501100000925","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["obgyn.onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Ultrasound in Obstet &amp; Gyne"],"published-print":{"date-parts":[[2025,6]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>Placental dysfunction can result in small\u2010for\u2010gestational age (SGA) or fetal growth restriction (FGR). The aim of this prospective cohort study was to assess the association of the cerebroplacental ratio (CPR) and other more conventional fetoplacental Doppler indices, circulating placental growth factor (PlGF) levels and soluble fms\u2010like tyrosine kinase\u20101 (sFlt\u20101)\/PlGF ratio, with specific placental abnormalities in a large cohort of pregnancies with an SGA\/FGR fetus.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      This was a prospective cohort study of singleton pregnancies with a SGA\/FGR fetus conducted at the Centre for Maternal and Fetal Medicine at the Mater Mother's Hospital, Queensland, Australia. Multivariable logistic regression with adjustment for pre\u2010eclampsia was used to evaluate the effect of CPR &lt;\u20095\n                      <jats:sup>th<\/jats:sup>\n                      \u2009centile, umbilical artery Doppler abnormality (defined as umbilical artery (UA) pulsatility index (PI) &gt;\u200995\n                      <jats:sup>th<\/jats:sup>\n                      \u2009centile, or absent or reversed end\u2010diastolic flow), mean uterine artery (UtA) PI &gt;\u200995\n                      <jats:sup>th<\/jats:sup>\n                      \u2009centile and abnormal placental biomarkers (PlGF level &lt;\u2009100\u2009ng\/L and sFlt\u20101\/PlGF ratio &gt;\u20095.78 if gestational age &lt;\u200928\u2009weeks or &gt;\u200938 if gestational age\u2009\u2265\u200928\u2009weeks) on the following placental abnormalities, classified based on the Amsterdam Placental Workshop Group Consensus criteria: placental maternal vascular malperfusion (MVM), fetal vascular malperfusion (FVM), villitis of unknown etiology (VUE), chronic histiocytic intervillositis (CHI) and delayed villous maturation (DVM).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      Among the 367 women included in this study, MVM was present in 159 (43.3%) placentae, FVM in 20 (5.4%), VUE in 49 (13.4%), DVM in 19 (5.2%) and CHI in six (1.6%). Compared to SGA controls with normal fetoplacental Doppler and placental biomarkers, CPR &lt;\u20095\n                      <jats:sup>th<\/jats:sup>\n                      \u2009centile (adjusted odds ratio (aOR), 3.17 (95%\u2009CI, 1.95\u20135.16);\n                      <jats:italic>P<\/jats:italic>\n                      \u2009&lt;\u20090.001), abnormal UA Doppler (aOR, 2.97 (95%\u2009CI, 1.80\u20134.90);\n                      <jats:italic>P<\/jats:italic>\n                      \u2009&lt;\u20090.001) and mean UtA\u2010PI &gt;\u200995\n                      <jats:sup>th<\/jats:sup>\n                      \u2009centile (aOR, 5.42 (95%\u2009CI 2.75\u201310.70);\n                      <jats:italic>P<\/jats:italic>\n                      \u2009&lt;\u20090.001) were associated with higher odds of placental abnormality. The odds of MVM specifically were significantly higher when CPR &lt;\u20095\n                      <jats:sup>th<\/jats:sup>\n                      \u2009centile (aOR, 2.47 (95%\u2009CI, 1.64\u20134.33);\n                      <jats:italic>P<\/jats:italic>\n                      \u2009&lt;\u20090.001), abnormal UA Doppler (aOR, 3.13 (95%\u2009CI, 1.91\u20135.12);\n                      <jats:italic>P<\/jats:italic>\n                      \u2009&lt;\u20090.001) or mean UtA\u2010PI &gt;\u200995\n                      <jats:sup>th<\/jats:sup>\n                      \u2009centile (aOR, 4.01 (95%\u2009CI, 2.25\u20137.13);\n                      <jats:italic>P<\/jats:italic>\n                      \u2009&lt;\u20090.001) was present. The odds of placental abnormality were also significantly higher if PlGF levels were &lt;\u2009100\u2009ng\/L (aOR, 3.66 (95%\u2009CI, 2.22\u20136.06);\n                      <jats:italic>P<\/jats:italic>\n                      \u2009&lt;\u20090.001) or the sFlt\u20101\/PlGF ratio was elevated (aOR, 3.74 (95%\u2009CI, 2.17\u20136.43);\n                      <jats:italic>P<\/jats:italic>\n                      \u2009&lt;\u20090.001). The odds of MVM were also higher in women with PlGF &lt;\u2009100\u2009ng\/L (aOR, 2.89 (95%\u2009CI, 1.72\u20134.85);\n                      <jats:italic>P<\/jats:italic>\n                      \u2009&lt;\u20090.001) and elevated sFlt\u20101\/PlGF ratio (aOR, 3.15 (95%\u2009CI, 1.83\u20135.45);\n                      <jats:italic>P<\/jats:italic>\n                      \u2009&lt;\u20090.001).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>\n                      In pregnancies with SGA\/FGR fetus, mean UtA\u2010PI &gt;\u200995\n                      <jats:sup>th<\/jats:sup>\n                      \u2009centile, abnormal UA Doppler, CPR &lt;\u20095\n                      <jats:sup>th<\/jats:sup>\n                      \u2009centile, PlGF &lt;\u2009100\u2009ng\/L and elevated sFlt\u20101\/PlGF ratio were all strongly associated with placental abnormality, particularly MVM. \u00a9 2025 The Author(s).\n                      <jats:italic>Ultrasound in Obstetrics &amp; Gynecology<\/jats:italic>\n                      published by John Wiley &amp; Sons Ltd on behalf of International Society of Ultrasound in Obstetrics and Gynecology.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1002\/uog.29237","type":"journal-article","created":{"date-parts":[[2025,5,7]],"date-time":"2025-05-07T04:28:17Z","timestamp":1746592097000},"page":"749-760","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":17,"title":["Placental biomarker and fetoplacental\n                    <scp>Doppler<\/scp>\n                    abnormalities are strongly associated with placental pathology in pregnancies with small\u2010for\u2010gestational\u2010age fetus: prospective study"],"prefix":"10.1002","volume":"65","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-8585-2357","authenticated-orcid":false,"given":"J.","family":"Hong","sequence":"first","affiliation":[{"name":"Mater Research Institute University of Queensland  Brisbane Queensland Australia"},{"name":"School of Medicine The University of Queensland  Herston Queensland Australia"},{"name":"Department of Obstetrics and Gynecology, Faculty of Medicine University of Malaya  Kuala Lumpur Malaysia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"K.","family":"Crawford","sequence":"additional","affiliation":[{"name":"Mater Research Institute University of Queensland  Brisbane Queensland Australia"},{"name":"School of Medicine The University of Queensland  Herston Queensland Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"E.","family":"Cavanagh","sequence":"additional","affiliation":[{"name":"Mater Research Institute University of Queensland  Brisbane Queensland Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-4892-6748","authenticated-orcid":false,"given":"V.","family":"Clifton","sequence":"additional","affiliation":[{"name":"Mater Research Institute University of Queensland  Brisbane Queensland Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-0765-7780","authenticated-orcid":false,"given":"F.","family":"da Silva Costa","sequence":"additional","affiliation":[{"name":"School of Medicine and Dentistry Griffith University and Maternal Fetal Medicine Unit, Gold Coast University Hospital  Gold Coast Queensland Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"A. 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