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Is aneuploidy screening an efficient tool in embryo selection ?. Necati Fındıklı Istanbul International Hospital IVF Center. Best embryo. Symmetrical PNs with equal size, even PNB distribution On day 1: (25-27 hourn after insemination ) EC+
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Is aneuploidyscreening an efficienttool in embryoselection? Necati Fındıklı IstanbulInternationalHospital IVF Center
Bestembryo • SymmetricalPNswithequal size, even PNB distribution • On day 1: (25-27 hournafterinsemination) EC+ • On day 2: (41-44 hoursafterinsemination) 4 cells • On day 3: (66-71 hoursafterinsemination) 7-8 cells • Fragmentation is lessthan <%10 • No multinucleation
Bestembryo Neuber et al. 2003
AneuploidyScreening (PGD-AS)PreimplantationGeneticScreening (PGS) Detection of chromosomalconstitutionin an embryo made by examining arepresentative sample taken at a preimplantation stage of development.
NumericalChromosomalAbnormalities AdvancedMaternalAge (AMA) >37 , >35? RecurrentPregnancyLoss (RPL) >2? , >3? abortus; Gestationalage 20 – 22 weeks (500 g) RecurrentImplantationFailure (RIF) >2? , >3? Trials, >10 goodqualityembryos MaleFactor (MF) severe OAT, Azoospermia Klinefelter’ssyndrome … StructuralChromosomalAbnormalities Translocations Inversions … AneuploidyScreening
Without PGD-AS Misinterpretationbythepublic With PGD-AS
EmbryoViability • Ethiology of Infertility • Abnormaloocytematuration • Paternalfactors • Suboptimalcultureconditions • Chromosomaland/orgeneticabnormalities
Chromosome abnormalities in humans • Mature oocytes~25% • Spermatozoa ~10% • Embryos~ 40-70% • Spontaneous miscarriage ~ 50% • Live births ~0.5-1%
Causes of Aneuploidy Errors in mitosis (postzygotic) Errors in meiosis I & meiosisII Gametogenesis EarlyCelavageanddifferentiation
Causes of Aneuploidy SwangandHöög.2006
Errors in Meiosis Kuliev. 2002
Defective Spindle Chatzimeletiou et al. 2005
Errors in Mitosis Silber et al. 2003
Aneuploidy vs. Embryomorphology Fragmentation Multinucleation AsymmetricCleavage
Aneuploidy vs. Fragmentation • Chromosomalabnormality rate is 70-90% in embryoswith >35% fragmentation. • Aneuploidy rate does not increase, whereasmosaicismandother post-zygoticabnormalitiesincreaseswithfragmentation. Munne. 2007
Aneuploidy vs. cytoplasmicproblems • Presence of vacuolesanddarkinclusions is not associatedwithchromosomalabnormalities. • Embryoswithcytoplasmicconcentrationsshow 86% chromosomalabnormalities. Munne. 2007
Aneuploidy vs. dominant blastomeres • Usuallypolyploidorpolyploidmosaics. • Dominant blastomere is alsomultinucleated in manycases. Munne. 2007
TechnicalLimitations: Embryobiopsy • Differenttechniquesfor zona opening • (Mechanical-Chemical-Laser) • Requireshigh-skilledlaboratoryandstaff • 1-cell vs. 2 cells? (Survival vs. Reliability?)
TechnicalLimitations: Diagnosis • Whichchromosomes? • Cost? • Anuclearcells? • Can a biopsiedcellrepresenttheembryo ?
Sandalinaset al. 2001 Blastocysts vs. Aneuploidy
Evangelos et al. 2008 Cleavage vs. BlastocystCulture
Conclusions: • Successfulembryoselection is thebesttoolforhighimplantationrates. • Evenwiththebestembryoselectionapproach, 30-50% of embryos can still be chromosomallyabnormal.
Conclusions: • Blastocystselectionand transfer maydecreasetheoverallabnormality rate, but stillnumerousabnormalandmosaicembryosmayreachblastocyststage. • % mosaicembryostendtoincreasewithincreasingnumber of chromosomesanalyzed. Therefore, newembryoscoringsystemsthat can better define differences in mosaicismwilleventually be needed.
Conclusions: • PGD is an effectiveembryoselectiontool in caseswithsingle gene disordersandstructuralchromosomalabnormalities. On theotherhand, thepossiblebenefit of selectingembryoswith PGS stillneedsto be confirmedbynewstudies.