{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,14]],"date-time":"2026-09-14T07:05:45Z","timestamp":1789369545569,"version":"build-2803163510"},"reference-count":25,"publisher":"Wiley","license":[{"start":{"date-parts":[[2026,9,13]],"date-time":"2026-09-13T00:00:00Z","timestamp":1789257600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"},{"start":{"date-parts":[[2026,9,13]],"date-time":"2026-09-13T00:00:00Z","timestamp":1789257600000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":["obgyn.onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["BJOG"],"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>Foetal\u2010neonatal alloimmune thrombocytopaenia (FNAIT) is a rare disease, most commonly caused by maternal alloantibodies to human platelet antigen (HPA)\u20101a\u00a0that can result in severe bleeding. The present study was designed to determine the frequency of higher risk for HPA\u20101a alloimmunisation and development of FNAIT among a racially and ethnically diverse cohort of pregnant women.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Design<\/jats:title>\n                    <jats:p>Longitudinal, prospective, non\u2010interventional, natural history study.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Setting<\/jats:title>\n                    <jats:p>Conducted across 28 sites in North America and Europe.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Population<\/jats:title>\n                    <jats:p>Pregnant women (\u2265\u200918\u2009years) with no history of FNAIT.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>Blood samples were collected at 10\u201314\u2009weeks' gestation and a sequential screening algorithm applied: maternal HPA\u20101a\/1b genotyping, human leukocyte antigen [HLA]\u2010DRB3*01:01 allele status, anti\u2010HPA\u20101a antibody status and foetal HPA\u20101 genotype.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Main Outcome Measures<\/jats:title>\n                    <jats:p>Number of women at higher risk for HPA\u20101a alloimmunisation (i.e., those who are HPA\u20101b\/b, HLA\u2010DRB3*01:01 positive, anti\u2010HPA\u20101a antibody negative and carrying an HPA\u20101a\u2010positive foetus) that alloimmunise.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>Of the 14\u2009114 participants screened, 1.7% were HPA\u20101b\/1b genotype, which varied according to race and geography. Of 24 women at higher risk for FNAIT, five were lost to follow\u2010up with no post\u2010partum test for alloimmunisation. At Week 10 post\u2010partum, 2\/19 higher risk participants (11%; 95% confidence interval [CI]: 1.3%, 33.1%) demonstrated anti\u2010HPA\u20101a antibodies, while 17 remained negative. Pre\u2010existing anti\u2010HPA\u20101a antibodies were identified in 18 other HPA\u20101bb, DRB3*01:01 positive women at screening.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>This prospective study confirms the rarity of a population at higher risk for HPA\u20101a alloimmunisation and FNAIT, describes the risk among Black and Asian women, and establishes a rigorous methodology to assess for risk of HPA\u20101a immunisation.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/1471-0528.70326","type":"journal-article","created":{"date-parts":[[2026,9,14]],"date-time":"2026-09-14T06:31:13Z","timestamp":1789367473000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Population Prevalence and Incident\n                    <scp>HPA<\/scp>\n                    \u20101a Alloimmunisation in Pregnancy: A Prospective, Multi\u2010Ethnic, Natural History Study"],"prefix":"10.1111","author":[{"given":"Vasilis","family":"Sitras","sequence":"first","affiliation":[{"name":"Division of Obstetrics, Fetal Medicine Center Oslo University Hospital  Oslo Norway"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Emilie","family":"Vander Haar","sequence":"additional","affiliation":[{"name":"Division of Maternal Fetal Medicine, Department of Obstetrics and Gynecology Weill Cornell Medicine\u2010New York Presbyterian Hospital  New York New York USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-9124-390X","authenticated-orcid":false,"given":"Russell","family":"Miller","sequence":"additional","affiliation":[{"name":"Division of Maternal Fetal Medicine Columbia University Irving Medical Center  New York New York USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Gwen","family":"Allen","sequence":"additional","affiliation":[{"name":"Department of Obstetrics and Gynecology St Francis Medical Center  Lynnwood California USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-2885-7818","authenticated-orcid":false,"given":"Sara","family":"Alson","sequence":"additional","affiliation":[{"name":"Obstetric, Gynaecological and Prenatal Ultrasound Research, Department of Clinical Sciences Lund University  Lund Sweden"},{"name":"Department of Obstetrics and Gynaecology Skane University Hospital, Barnmorskestationen Roseng\u00e5rd  Malmo Sweden"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Roisin","family":"Armstrong","sequence":"additional","affiliation":[{"name":"Clinical Operations, Rallybio Inc.  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