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1.
Am J Transplant ; 17(12): 3149-3158, 2017 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-28597555

RESUMEN

We reported that current assignment of HLA-DQ is a barrier to organ allocation. Here we simulated the impact of incorporating HLA-DQ antigens and antibodies as A/B and αß allelic variants, respectively, on calculated panel reactive antibody (cPRA) and probability of finding potential compatible donors (PCD). A cohort of 1224 donors and 2075 sensitized candidates was analyzed using HLA-DQαß allelic (study) versus serologic (current practice) nomenclature. A significant (p < 10-4 ) decrease in cPRA was observed with higher impact for male versus female, and first transplant versus retransplant (p < 10-4 ), affecting mostly patients with moderate cPRA (30-80%). Consequently, the number of patients qualifying for 100% cPRA points according to the United Network for Organ Sharing-Kidney Allocation System decreased by 37%. More critically, by using allelic versus serologic nomenclature for HLA-DQ, the number of PCDs for all patients was increased, with male and first-transplant patients showing a higher expansion compared with female and retransplants. Patients of blood group O showed the highest benefit. The goal of reporting unacceptable antigens is to improve accuracy of virtual crossmatching and increase the likelihood of finding immunologically compatible donors. Our simulation provides strong support for the need to re-evaluate the use of allele typing and how HLA-DQ antigens and antibodies are incorporated into allocation policies to ensure equity.


Asunto(s)
Tipificación y Pruebas Cruzadas Sanguíneas/normas , Selección de Donante/legislación & jurisprudencia , Antígenos HLA-DQ/inmunología , Isoanticuerpos/inmunología , Trasplante de Riñón , Asignación de Recursos/legislación & jurisprudencia , Donantes de Tejidos , Estudios de Cohortes , Selección de Donante/normas , Femenino , Estudios de Seguimiento , Tasa de Filtración Glomerular , Humanos , Isoanticuerpos/sangre , Pruebas de Función Renal , Masculino , Persona de Mediana Edad , Pronóstico , Factores de Riesgo , Obtención de Tejidos y Órganos/métodos
2.
C R Seances Soc Biol Fil ; 183(5): 457-60, 1989.
Artículo en Francés | MEDLINE | ID: mdl-2534745

RESUMEN

Excessive daily sleepiness attribute to sleep disturbances can be a problem for occupational physician concerning the work ability to security works, night shift work and vehicle driving. It's difficult to detect those pathologies because the workers don't identify their symptoms as serious diseases or because they mask these symptoms for fear of the loose of their job. We've studied one case of SAS (sleep apnea syndrome) and one case of narcolepsy to demonstrate: 1) the criterions of the occupational forecast; 2) the sometimes serious social and occupational consequences of a medical inaptitude sanction. We insist on the necessity of a good collaboration between general practitioner and occupational physician.


Asunto(s)
Medicina del Trabajo , Trastornos del Sueño-Vigilia/complicaciones , Evaluación de Capacidad de Trabajo , Adulto , Humanos , Masculino , Persona de Mediana Edad , Narcolepsia/complicaciones , Síndromes de la Apnea del Sueño/complicaciones
3.
Pathol Biol (Paris) ; 51(6): 314-28, 2003 Aug.
Artículo en Francés | MEDLINE | ID: mdl-12927889

RESUMEN

Cytogenetic studies of acute myeloid leukaemias reveal non-random chromosomal abnormalities in 50-70% of karyotypes. Some are correlated with morphological and immunological parameters and constitute a prognostic factor independent of the other factors of risk: favourable for acute leukaemias myeloid with translocations t(8;21), t(15;17) and inversion or translocation of the chromosome 16, inv(16)/t(16;16), poor with deletion of the long arm of chromosome 5 del(5q), rearrangement of the 11q23 region and complex karyotypes. The distribution of the anomalies depends on the age: 11q23 and t(8;21) more frequent for the child, del(5q) and complex anomalies more frequent for the adult. The karyotypes are essential for the diagnosis, the follow-up of the patients and the evaluation of the relapse. It plays a fundamental part in the detection of new genes and their partners implied in the leucemogenese. The knowledge of their function is essential to open new therapeutic ways.


Asunto(s)
Aberraciones Cromosómicas , Leucemia Mieloide Aguda/genética , Citogenética , Eliminación de Gen , Humanos , Cariotipificación , Monosomía , Pronóstico , Translocación Genética , Trisomía
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