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1.
Eur J Hum Genet ; 21(12): 1361-8, 2013 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-23531862

RESUMEN

Preimplantation Genetic Diagnosis (PGD) is a method of testing in vitro embryos as an alternative to prenatal diagnosis with possible termination of pregnancy in case of an affected child. Recently, PGD for hereditary breast and ovarian cancer caused by BRCA1 and BRCA2 mutations has found its way in specialized labs. We describe the route to universal single-cell PGD tests for carriers of BRCA1/2 mutations. Originally, mutation-specific protocols with one or two markers were set up and changed when new couples were not informative. This route of changing protocols was finalized after 2 years with universal tests for both BRCA1 and BRCA2 mutation carriers based on haplotyping of, respectively, 6 (BRCA1) and 8 (BRCA2) microsatellite markers in a multiplex PCR. Using all protocols, 30 couples had a total of 47 PGD cycles performed. Eight cycles were cancelled upon IVF treatment due to hypostimulation. Of the remaining 39 cycles, a total of 261 embryos were biopsied and a genetic diagnosis was obtained in 244 (93%). In 34 of the 39 cycles (84.6%), an embryo transfer was possible and resulted in 8 pregnancies leading to a fetal heart beat per oocyte retrieval of 20.5% and a fetal heart beat per embryonic transfer of 23.5%. The preparation time and costs for set-up and validation of tests are minimized. The informativity of microsatellite markers used in the universal PGD-PCR tests is based on CEPH and deCODE pedigrees, making the tests applicable in 90% of couples coming from these populations.


Asunto(s)
Proteína BRCA1/genética , Proteína BRCA2/genética , Neoplasias de la Mama/diagnóstico , Neoplasias de la Mama/genética , Mutación/genética , Neoplasias Ováricas/diagnóstico , Neoplasias Ováricas/genética , Adulto , Femenino , Humanos , Masculino , Repeticiones de Microsatélite/genética , Linaje , Embarazo , Diagnóstico Preimplantación/métodos , Diagnóstico Prenatal/métodos
2.
Hum Reprod ; 22(8): 2243-8, 2007 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-17584750

RESUMEN

BACKGROUND: Although rare, microbial contamination of culture dishes occasionally occurs in our IVF/ICSI programme. Despite stringent culture conditions and the use of medium containing penicillin and streptomycin, an increasing number of infections was observed once they were routinely recorded. In this study, 95 cases of contaminated culture dishes were examined, in an attempt to identify possible causes. METHODS: Relevant data of the IVF/ICSI treatment cycles and the micro-organisms isolated from the infected culture dishes were evaluated retrospectively. RESULTS: Infections were observed only in IVF culture dishes and never after applying intra-cytoplasmic sperm injection. Identification of the contaminating micro-organisms showed that infections were mainly caused by Escherichia coli (n = 56; 58.9%) and Candida species (n = 24; 25.3%). Of the E. coli strains isolated, 41 (73.2%) appeared to be resistant to both antibiotics used in the culture medium and 13 (23.2%) appeared to resist either penicillin or streptomycin. Of all bacterial strains isolated, the resistances were 61.4% to both and 30% to one of the antibiotics used. CONCLUSIONS: Applying the ICSI procedure prevents colonization of the culture dishes by micro-organisms. Infections in IVF culture dishes are mainly caused by bacterial strains insensitive to the antibiotics used or due to yeast colonization by Candida species which frequently reside in the vagina.


Asunto(s)
Fertilización In Vitro , Oocitos/microbiología , Semen/microbiología , Inyecciones de Esperma Intracitoplasmáticas , Candida/aislamiento & purificación , Técnicas de Cultivo de Embriones/normas , Escherichia coli/aislamiento & purificación , Femenino , Humanos , Masculino , Estudios Retrospectivos
3.
Fertil Steril ; 81(3): 693-6, 2004 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-15037424

RESUMEN

OBJECTIVE: To find the underlying defect in a case of primary FSH deficiency and to estimate the beneficial effect of FSH treatment. DESIGN: Case report. SETTING: University hospital fertility clinic. PATIENT(S): Normal, healthy, 37-year-old male patient with severe oligoteratozoospermia. INTERVENTION(S): Levels of FSH, LH, LHRH provocation test, karyotyping, genomic analysis on the Y-chromosomal AZF region and sequencing of the FSHB gene, FSH treatment. MAIN OUTCOME MEASURE(S): We compiled detailed clinical and molecular data on four pregnancies. We compare this case with a similar case published recently. RESULT(S): There were detectable but very low FSH levels after LHRH provocation; the LH response was not entirely normal, and no genomic abnormalities were found in the FSHB gene. The FSH treatment resulted in four pregnancies, two of which ended in abortion; the other two resulted in the birth of two healthy children. Both our case and the published case had detectable but abnormally low FSH levels on some occasions, but normal or highly normal inhibin B levels that differed from the expected low levels. Both patients had a normal male phenotype and no detectable mutation in the FSHB gene. The published case differed from our patient in that the published case was azoospermic whereas ours was extremely oligoteratozoospermic. The beneficial effect of FSH treatment was only shown in our patient. CONCLUSION(S): The published case and ours may have a common, as yet unidentified, underlying defect. The dramatic and immediate effect of FSH treatment on our patient's fertility was clearly demonstrated.


Asunto(s)
Hormona Folículo Estimulante/deficiencia , Hormona Folículo Estimulante/uso terapéutico , Hormonas/deficiencia , Hormonas/uso terapéutico , Infertilidad Masculina/tratamiento farmacológico , Infertilidad Masculina/etiología , Oligospermia/etiología , Adulto , ADN/genética , Femenino , Hormona Folículo Estimulante/sangre , Hormona Folículo Estimulante de Subunidad beta/genética , Hormonas/sangre , Humanos , Masculino , Errores Innatos del Metabolismo/complicaciones , Embarazo , Resultado del Tratamiento
4.
Hum Reprod ; 18(2): 460-1; author reply 461, 2003 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-12571193
5.
Reprod Biomed Online ; 7(6): 691-4, 2003 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-14748969

RESUMEN

Unlike most medical laboratories that play a diagnostic role, laboratories for assisted reproductive technologies, ART laboratories, are involved in the treatment of infertile couples. Handling human gametes and producing human embryos in order to achieve much-sought pregnancies form the key tasks of an ART laboratory. The impact of the activities and the possible risks makes it necessary to ensure the safety and reproducibility of all methods. To achieve and maintain the highest level of patient care and the highest success rates, a quality management system should be implemented. Several guidelines, compiled by professional associations of ART experts, official international standards and quality management models have been developed and issued and can be applied. Irrespective of the choice, establishing a quality management system in an ART laboratory leads to a huge amount of additional work and requires a lot of investment in all kind of areas. However, due to the increased standardization and efficiency of all procedures as well as the improved transparency and traceability of all actions performed, the quality of service provided by the laboratory will improve substantially and the effort will be worthwhile.


Asunto(s)
Técnicas Reproductivas Asistidas/normas , Humanos , Laboratorios/normas , Control de Calidad
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