Publication:
Fine-tuning blastocyst selection based on morphology: a multicentre analysis of 2461 single blastocyst transfers

dc.contributor.coauthorStorr, Ashleigh
dc.contributor.coauthorCooke, Simon
dc.contributor.coauthorGarrett, Don
dc.contributor.coauthorVenetis, Christos A.
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorBilir, Esra
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2024-11-09T22:55:58Z
dc.date.issued2019
dc.description.abstractResearch question: Which blastocyst morphology parameter is associated with live birth after controlling for female age and endometrial receptivity? Design: Retrospective study including fresh single blastocyst transfers (n = 2461) where the value of serum progesterone on day of human chorionic gonadotrophin trigger (PdHCG) was available. Generalized estimating equation regression models evaluated the independent effects of developmental stage (DevSt), inner cell mass (ICM) and trophectoderm grade on live birth rates while controlling for the confounding effects of female age and PdHCG. Results: DevSt was strongly associated with the probability of live birth (P < 0.0001) independently of female age (odds ratio [OR] 0.89, 95% confidence interval [CI] 0.87-0.91) and PdHCG (OR 0.80, 95% CI 0.74-0.87). For full blastocysts, expanded blastocysts and hatching blastocysts, addition of ICM and trophectoderm grading in the multivariable analysis suggested that besides female age (OR 0.92, 95% CI 0.90-0.94) and PdHCG (OR 0.80, 95% CI 0.73-0.87), only DevSt (P = 0.001) and trophectoderm quality (P = 0.004) were independent predictors of live birth, while the predictive capacity of ICM was no longer significant. The mean probability of live birth was highest for AA blastocysts (35.0%), followed by BA blastocysts (31.2%) and AB blastocysts (27.7%). Conclusion: This large study analyses for the first time the independent role of blastocyst morphology in predicting live birth while controlling for female age and PdHCG. Its findings suggest that DevSt and then trophectoderm grade are stronger predictors of live birth over ICM grade when selecting a single blastocyst for transfer.
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.issue4
dc.description.openaccessNO
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipIVF Australia
dc.description.sponsorshipNHMRC Early Career Fellowship [GNT1147154] The authors would like to thank IVF Australia for its support in this study No funding was received for this study CA Venetis is supported by an NHMRC Early Career Fellowship (GNT1147154).
dc.description.volume39
dc.identifier.doi10.1016/j.rbmo.2019.06.008
dc.identifier.eissn1472-6491
dc.identifier.issn1472-6483
dc.identifier.quartileQ1
dc.identifier.scopus2-s2.0-85071954106
dc.identifier.urihttps://doi.org/10.1016/j.rbmo.2019.06.008
dc.identifier.urihttps://hdl.handle.net/20.500.14288/7283
dc.identifier.wos488774100007
dc.keywordsBlastocyst
dc.keywordsDevelopmental stage
dc.keywordsLive birth
dc.keywordsMorphology
dc.keywordsTrophectoderm
dc.language.isoeng
dc.publisherElsevier Sci Ltd
dc.relation.ispartofReproductive Biomedicine Online
dc.subjectObstetrics
dc.subjectGynecology
dc.subjectReproductive biology
dc.titleFine-tuning blastocyst selection based on morphology: a multicentre analysis of 2461 single blastocyst transfers
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorBilir, Esra
local.publication.orgunit1SCHOOL OF MEDICINE
local.publication.orgunit2School of Medicine
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