Searched for: person:grifoj01
Uterine transplantation, abdominal trachelectomy, and other reproductive options for cancer patients
del Priore G; Smith JR; Boyle DC; Corless DJ; Zacharia FB; Noakes DA; Diflo T; Grifo JA; Zhang JJ
More and more women with cancer issues are now raising fertility concerns as survival improves and childbearing is delayed. Pregnancy is no longer contraindicated in cancer patients including breast and endometrial cancer survivors. In fact, survival in patients treated for breast cancer who subsequently become pregnant is actually higher than that in patients who do not become pregnant. 'Therapeutic' abortions are no longer recommended. Assisted reproductive technology (ART) have been associated with ovarian neoplasms, but the association is probably not causal. Neither ART nor hormone replacement is contraindicated in cancer patients. Our institution is very supportive of patients and the difficult decisions cancer survivors face. Using a program of counseling and close collaboration between oncologists, perinatologists, and reproductive endocrinologists, informed patients are offered every possible option, including ART and uterine transplantation, to achieve their family planning objectives
PMID: 11594549
ISSN: 0077-8923
CID: 26646
Fertility and maternal age strategies to improve pregnancy outcome
Krey L; Liu H; Zhang J; Grifo J
In humans, the live birth rate drops precipitously with increasing maternal age, and this decline is associated with increases in the incidence of oocyte and embryo aneuploidy. Preimplantation aneuploidy screening has improved pregnancy outcome by significantly lowering the miscarriage rate. Nevertheless, aneuploidy screening only identifies the affected embryos; it does not attempt to correct the underlying biologic problem. Anomalies in chromosome segregation can result from a dysfunctional first or second meiotic division in the egg or develop after fertilization during the first few mitoses of early embryonic development. In both instances, ooplasmic anomalies may account for the nuclear problem. Low cell levels of cytoplasmic proteins (e.g., cytoskeletal elements, enzymes, energy stores, cell cycle regulatory proteins) may lead to a dysfunctional division of chromosomes during egg maturation or following fertilization. Ooplasmic injection is a micromanipulation technique that has produced pregnancies in patients with a history of poor-quality, fragmented embryos. Germinal vesicle transfer is a research procedure used to investigate the ooplasmic-nuclear interplay regulating cell cycle, maturation, and fertilization. Both these techniques may prove to be effective in improving the quality of eggs from patients of advanced maternal age
PMID: 11594545
ISSN: 0077-8923
CID: 26647
Cell cycle checkpoint proteins Bub1 and Mad2 localize to kinetochores during meiosis in mouse oocytes [Meeting Abstract]
Blaszczyk, A; Brockmann, C; Grifo, J; Krey, L
ISI:000170863900733
ISSN: 0015-0282
CID: 54928
Developmental potential and blastocyst formation rate in human embryos with early stage development delay, arrest, or with multinucleated blastomere (MNB) [Meeting Abstract]
Chi, L; DeJesus, E; McCaffery, C; Grifo, JA; Berkeley, AS; Krey, LC
ISI:000170863900504
ISSN: 0015-0282
CID: 54925
Preimplantation genetic diagnosis of cystic fibrosis (CF) with compound heterozgote S549R/DF508 [Meeting Abstract]
Tang, Y; Krey, L; Adler, A; Chi, L; Grifo, J
ISI:000170863900359
ISSN: 0015-0282
CID: 54920
The nuclear developmental capacity of mouse oocytes following cryopreservation at germinal vesicle stage [Meeting Abstract]
Liu, H; Krey, LC; Zhang, J; Grifo, JA
ISI:000170863900212
ISSN: 0015-0282
CID: 54917
The impact of severe oligospermia on blastocyst formation in IVF-ICSI [Meeting Abstract]
Adler, A; McCaffrey, C; Lu, L; Noyes, N; Grifo, J; Krey, L
ISI:000170863900026
ISSN: 0015-0282
CID: 54913
Factors useful in predicting the success of oocyte donation: a 3-year retrospective analysis
Noyes N; Hampton BS; Berkeley A; Licciardi F; Grifo J; Krey L
Objective: To establish prognostic relevance of parameters assessed in oocyte donation cycles.Design: Retrospective analysis.Setting: Large university-based donor oocyte program.Patient(s): All oocyte recipient cycles achieving embryo transfer from September 1995 to October 1998.Intervention(s): None.Main Outcome Measure(s): Pregnancy.Result(s): Recipient age and reproductive status, day 9 and 12 serum estradiol (E(2)) levels and a progesterone (P) level obtained 2 days after initiation of hormonal therapy did not correlate with pregnancy. Endometrial thickness, but not endometrial pattern, was useful in predicting pregnancy outcome. The clinical pregnancy and live-birth rate in cycles where the endometrial thickness was less than 8 mm was significantly lower when compared to cycles with an endometrial thickness >/=9 mm. Cycles where optimal quality embryos were transferred had the highest implantation (36%), clinical pregnancy (63%) and live birth (54%) rates and these rates were significantly higher than those of cycles where only poor quality embryos were available for transfer (10% implantation, 17% clinical pregnancy, and 8% live birth rates, respectively; P<.05).Conclusion(s): The most reliable predictive factors for pregnancy in oocyte donation cycles are the quality of the embryos transferred and the recipient's mid-cycle endometrial thickness. Recipient monitoring should minimally include ultrasound assessment of endometrial thickness
PMID: 11438325
ISSN: 0015-0282
CID: 21151
A two- versus three-embryo transfer: the oocyte donation model
Licciardi F; Berkeley AS; Krey L; Grifo J; Noyes N
OBJECTIVE: To compare implantation and pregnancy rates in oocyte recipients undergoing a two-embryo versus three-embryo transfer, 3 days after retrieval. DESIGN: Retrospective comparative analysis. SETTING: University-based in vitro fertilization center. PATIENT(S): All oocyte recipients undergoing embryo transfer from January 1, 1997 through August 31, 1999. INTERVENTION(S): Recipients received two or three embryos. MAIN OUTCOME MEASURE(S): Implantation, and clinical and multiple pregnancy rates. RESULT(S): Seventy-three recipients underwent a two-embryo transfer, and 376 had three embryos replaced. The numbers of oocytes retrieved (12.7 +/- 0.89 vs. 13.1 +/- 0.36) and embryos obtained (8.05 +/- 0.65 vs. 8.77 +/- 0.27) did not differ between the two-embryo and three-embryo transfer groups, nor did the proportion of patients with embryo cryopreservation (54.3% vs. 42.6%, respectively). There was no significant difference in pregnancy or implantation rates when comparing those patients with a two-embryo transfer to those with a three-embryo transfer. Significantly, 13.8% of the pregnancies in the three-embryo transfer group were triplet. CONCLUSION(S): Reducing the number of embryos transferred in an oocyte donation cycle can lower the incidence of triplet pregnancies without significantly lowering the overall pregnancy rate
PMID: 11239533
ISSN: 0015-0282
CID: 26775
Poor embryo quality: The answer lies (mostly) in the egg [Editorial]
Krey, L C; Grifo, J A
PMID: 11239524
ISSN: 0015-0282
CID: 120773