New developments in reproductive medicine
Transcript of New developments in reproductive medicine
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New Developments in New Developments in
Reproductive MedicineReproductive Medicine
Prof. Dr. med. K. DiedrichDept. of Obstetrics & Gynecology
University of Schleswig-Holstein, Campus Lübeck, Germany
Infertility Meeting, Misurata, 26th October 2007
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Number of infertile couples in Germany:
approx. 15 - 20% of all couples(1.2 – 1.6 Millions)
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Once upon a time…
07/78 Louise Brownwas born
Birth after reimplantation of a human embryo
Steptoe P.C. / Edwards R.G.Lancet 2 (1978): 366
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Milestones in reproductive medicine• 1960 - ovarian stimulation with clomifene and gonadotrophins
- radioimmunoassay• 1970 - secretion, synthesis, mechanism of GnRH a. gonadotrophins
- in vitro fertilisation• 1980 - GnRH-agonists and gonadotrophins
- cryopreservation• 1990 - recombinant gonadotrophins
- preimplantation genetic diagnosis- intracytoplasmatic sperm injection (ICSI)
- GnRH-antagonists• 2000 - in vitro maturation of oocytes
- embryonic stemcells- SET (single embryo transfer)
- vitrification
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Probability of successfull infertility treatmentafter: Dor et al., 1996
cause of infertility pregnancy rate
ovarian 57.7%
tubal 63.3%
male 71.4%
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• 1.9 Millions after ivF
• 800 000 after ICSI
• Germany (1982-2004): 108 000
Children after ART until 2004 worldwide
C. Nygren, 2004
birthrate per cycle:- after ivF 21% (DIR, 2004)
- after in vivo fertilisation 24%
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New Developments in Reproductive Medicine
• Ovarian stimulation: GnRH-antagonists
• Elective single embryotransfer (eSET)
• Blastocyst transfer
• In-vitro-maturation
• Cryopreservation and vitrification
• Preimplantation genetic diagnosis and screening
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History of ovarian stimulation• 1970 Clomifen
hMG
• 1980 GnRH-agonist / hMG
• 1990 recFSHGnRH-antagonist / hMG or recFSH
• 2000 long acting FSH
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Structure of GnRH and analogues
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0
2
4
6
8
AmpoulesGonadotropins
d 6
Menses
Cetrorelix
OPU
HCG
0 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17
ET
day of cycle
-16 -14 -12 -10 -8 -6 -4 -2 0 2 4 6 8 10 12 14 16
0
2
4
6
8
Ampoules HMG
OPU
d -14
LHRH-agonist: daily injection/ depot/ nasal spray
Menses
ET
HCG
17 day of cycle
„long protocol“
„Lübeck protocol“
GnRH-agonist and antagonist protocol
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Citation Year Effect Lower Upper PValue
Albano 2000 ,829 ,444 1,547 ,556
European 2000 ,748 ,519 1,078 ,119
Olivennes 2000 ,799 ,336 1,901 ,612
North American 2001 ,777 ,470 1,284 ,324
Middle East 2001 ,973 ,604 1,568 ,910
Akman 2001 ,760 ,177 3,263 ,712
Hohmann 2003 ,929 ,398 2,169 ,865
Martinez 2003 1,569 ,307 8,011 ,587
Franco 2003 ,545 ,065 4,562 ,573
Hwang 2004 1,105 ,347 3,526 ,866
Sauer 2004 1,067 ,334 3,409 ,913
Xavier 2005 ,845 ,288 2,484 ,760
Loutradis 2005 ,704 ,271 1,827 ,469
Malmusi 2005 1,000 ,257 3,888 1,000
Marci 2005 10,358 ,533201,451 ,062
Cheung 2005 1,550 ,242 9,940 ,642
Check 2005 1,818 ,518 6,382 ,347
Barmat 2005 ,651 ,262 1,621 ,356
Bahceci 2005 ,839 ,436 1,613 ,598
Badrawi 2005 ,803 ,320 2,015 ,640
Schmidt 2005 1,000 ,181 5,533 1,000
Lee 2005 ,696 ,229 2,114 ,522
FixedCombined (22) ,859 ,722 1,021 ,085
0,1 0,2 0,5 1 2 5 10
Favor agonists Favor antagonists
Odds ratio:0.859
p=0.085
LIVE BIRTH
Rate difference
2.7%Griesinger et al., 2006
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- simple stimulation- fixed initiation of GnRH-antagonist on day 6- no LH supplementation- no increase of gonadotrophin dose at GnRH-
antagonist initiation- ovulation induction for ART by dominant follicle of
≥ 17mm- luteal phase supplementation is mandatory
Advantages of GnRH-antagonists
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- fits into the normal cycle(„the patients like it“)
- less side effects in comparison to the long protocol:1. Ø cysts2. Ø hormonal withdrawl3. less OHSS
- no significant difference in the probability of live birth between GnRH-agonists and antagonists
Advantages of GnRH-antagonists
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long acting FSH
1 2 3 4 5 6 7 8 9 10 11 12 13 14 ….
FSH-CTP
10000 IE hCG
follicle aspirationafter 36h
GnRH-Antagonist
LF 10 mm LF 14 mm LF 17mm
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Children after ART: 1997-2002
DIR 2001
IVF ICSI Total %
Singleton 11455 12096 23551 59.83
Twin 6782 6553 13335 33.87
Triplet 1228 1221 2449 6.22
Quadruplet 23 8 31 0.08
Total 19488 19878 39366 100
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Problems of multiple pregnancies
• pregnancy related diseases
• prematurity
• increase of neonatal morbidity and mortality
• costs
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Aims
1. To avoid multiple pregnancies
2. Improve the pregnancy and life birth rate
Solution: Transfer of one selected embryo
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Embryo selection
> 30% < 5%Implantation
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eSET = 40.3% pregnancy rate
1% gemini
eDET = 44% pregnancy rate
32% gemini
Pregnancy rate after elective single embryo transfer (eSET) and
elective double embryo transfer (eDET)
Gerris, 2005ESHRE
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Karlström u. Bergh, HumRep 22: 2007
Birth rate and MBR in relation to the percentage of SETand triple embryo transfer (TET) in Sweden 1991–2004
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Karlström u. Bergh, HumRep 22: 2007
Birth per embryo transfer (%) and MBR in Sweden and USA
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§ 1, Abs. 1, Nr. 5„a person fertilizing more oocytes than he or she intends to tranfer in the course of one treatment cycle“
§ 1, Abs. 1, Nr. 3„a person transfering more than 3 embryos to the womb in the course of one treatment cycle“
Prison sentence up to three years or financial penalty for
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Blake et al. 2004
• no significant difference (OR=0,91; 95% CI 0,71-1,17)
• disadvantage of long-term cultivation
Metaanalysis of blastocyst transfer: day 2/3 versus day 5/6 of embryo transfer
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Preimplantation genetic screening (PGS)University of Brussels
Inclusion criteria:
• 37 yrs and older
• prospective randomized controlled study
• examined chromosomes: X, Y, 13, 18, 21
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Results PG-Screening University of Brussels
Preimplantation genetic screening (PGS) control
Patients 86 82
Embryo transfer 48 (55%) 70 (85%)
Abnormal embryos 20
Pregnancies per embryo transfer 10 (20.9%) 18 (26.5%)
No of embryos per ET 2.1 (100) 3.1 (210)
Implantation rate per embryo 10% 8%
Devroey, 2006
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Conclusion of the Brussels study:
A positive effect of PGS on implantation and
abortion rate of this study and others is not clearly
documented.
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Methods of cryopreservation
slow cooling
vitrification
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Clin. pregnancies / ETafter cryo transfer
(1996-2004)
Cryo transfer 67,257
Clin. pregnancy / ET 15.5 %
Abortion rate after cryo transfer 21.64 %
German IVF Index 2004
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after Kuwayama, RBM-online 2005, pp.300-308
a. Polypropylen strip
b. Hartplastik-Griffstück
d. Schutz für LN2 Lagerung
c. Hartplastik-Schutzhülle
Cryotop for vitrification
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Lübeck Results (till 01/2007)
Slow-cooling Vitrifikation0%
20%
40%
60%
80%
100%
59%
91%
Slow-cooling Vitrifikation0%
10%
20%
30%
40%
50%
19%
34%
survival rate pregnancy rate
n=752 n=155
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The Lancet 1965
„Oocytes from antral follicles can
finalize their meiotic maturation in
vitro in 24 – 48 hours“
R.G. Edwards et al.
First oocyte maturation in vitro
Edwards RG et al. 1965
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Development of IVM
1983 Veeck First birth after IVM
1991 Cha IVM on immature oocyte extracted by using ovarian biopsy during a cesarean section resulted in healthy twins
2000 Cha birth of 20 healthy children afte IVM
2003 Mikkelsen birth of 33 healthy children after IVM
today >300 children after IVM
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Early oocyte retrieval from antral follicles before
selection and atresia . . .
Physiological basics of IVM
day 3 day 8 - 12
d>10mm
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• PCOS
• high responder with a risk for OHSS
• normo-cyclic patients
• cryopreservation of oocytes (oncology)
• low responder
• implantation failure
Therapeutic indications for IVM
Mikkelsen et al. 2003, Smitz 2005, von Otte 2005
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IVMoocyte
maturation (24 h)
Tag 1 2 3 4 5 6 7 8 9 10 ….
first Examination:
basicultrasound
and hormone
level
embryo
culture
(2- 3 days)
Embryotransfer 2-3 days after
ovum aspiration
Menses
Fertilizationvia ICSI
♂ Male: sperms
4 days
of low dose hMG
(„priming“ with
75IE hMG/day)
Exam. 2,3, …
ultrasound and
hormone level
primordial follicle
≥ 12mm and E ≥7mm
10.000 IE hCG
36h later aspiration of small antral
follicles
Estradot 100
Crinone 8%
Treatment protocol
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Fertilization and outcome
N= 100 cycles total % Mean ± SD
Mature oocytes/ ovum aspiration 310 4.2 ± 3.4
Pronuclei/ ovum aspiration 138 44 1.77 ± 1.44
Cycles with embryo transfers 55/85 67%
Embryos/ transfer 122 2.2
Pregnancies/ transfer 13 13%
Cryopreservation 4 5.9%
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• ovarian biopsy and
cryopreservation
• in vitro Growth („IVG“)
followed by In vitro
Maturation („IVM“)
in the future: „TESE“ for the woman?
Oktay et al. 2004
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Future of Reproductive Medicine• new embryo protection law (european?)
• improvement of pregnancy rate by the elective single
embryo transfer (morphological criteria)
• avoid multiple pregnancies
• vitrification
• in vitro maturation
• aim of infertility treatment: simple, safe, comfortable,
successful and cheap