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2.
Mult Scler Relat Disord ; 45: 102427, 2020 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-32841868

RESUMEN

BACKGROUND: Comorbidities can impose diagnostic and treatment challenges in patients with multiple sclerosis (MS). Sickle cell disease (SCD) and MS are both inflammatory diseases featuring immune system dysregulation, and the reciprocal interaction of these diseases deserves investigation. METHODS/RESULTS: We present the case of a 28-year-old woman with SCD who developed a sickle cell crisis and acute chest syndrome during corticosteroid treatment for a first MS attack. We then provide a review of the literature on co-management of SCD and MS. In patients with SCD experiencing an acute MS exacerbation, pre-treatment with red blood cell exchange transfusion before corticosteroids may reduce adverse vaso-occlusive events. Plasma exchange may also be considered. Finally, we discuss innovative pre-clinical research that suggests that natalizumab or dimethyl fumarate may ameliorate SCD symptoms while preventing MS relapses; human trials, however, are needed. CONCLUSION: The co-occurrence of inflammatory disorders, in this case MS and SCD, requires providers to appropriately manage each condition with consideration of the other. Future studies may generate shared avenues for treatment.


Asunto(s)
Síndrome Torácico Agudo , Anemia de Células Falciformes , Esclerosis Múltiple , Adulto , Anemia de Células Falciformes/complicaciones , Anemia de Células Falciformes/terapia , Femenino , Humanos , Esclerosis Múltiple/complicaciones , Esclerosis Múltiple/tratamiento farmacológico
3.
Arch Cardiovasc Dis ; 112(3): 187-198, 2019 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-30594574

RESUMEN

There is limited information about differences in maternal deaths from peripartum cardiomyopathy (PPCM) between advanced and developing countries. To review the literature to define the global prevalence of death from PPCM, and to determine the differences in PPCM mortality rates and risk factors between advanced and developing countries. Studies in the English language reporting mortality data on patients with PPCM were included from searches of MEDLINE, Embase, CINAHL, the Cochrane Library, the Web of Science Core Collection and Scopus from 01 January 2000 to 11 May 2016. Of the 4294 articles identified, 1.07% were included. The primary outcome was death; rates of heart transplant, acute myocardial infarction, heart failure, arrhythmia, cerebrovascular events, embolism and cardiac arrest were recorded. Studies were categorized as having been conducted in advanced or developing countries. Data from 46 studies, 4925 patients and 13 countries were included. There were 22 studies from advanced countries (n=3417) and 24 from developing countries (n=1508); mean follow-up was 2.6 (range 0-8.6) years. Overall mortality prevalence was 9% (95% confidence interval [CI] 6-11%). The mortality rate in developing countries (14%, 95% CI 10-18%) was significantly higher than that in advanced countries (4%, 95% CI 2-7%). There was no difference in the prevalence of risk factors (chronic hypertension, African descent, multiple gestation and multiparity) between advanced and developing countries. Studies with a higher prevalence of women of African descent had higher death rates (correlation coefficient 0.29, 95% CI 0.13-0.52). The risk of death in women with PPCM was higher in developing countries than in advanced countries. Women of African descent had an increased risk of death.


Asunto(s)
Cardiomiopatías/mortalidad , Países Desarrollados , Países en Desarrollo , Disparidades en el Estado de Salud , Mortalidad Materna , Periodo Periparto , Trastornos Puerperales/mortalidad , Adolescente , Adulto , Población Negra , Cardiomiopatías/diagnóstico , Cardiomiopatías/etnología , Cardiomiopatías/terapia , Femenino , Humanos , Masculino , Persona de Mediana Edad , Embarazo , Prevalencia , Trastornos Puerperales/diagnóstico , Trastornos Puerperales/etnología , Trastornos Puerperales/terapia , Medición de Riesgo , Factores de Riesgo , Adulto Joven
4.
AIDS ; 32(3): 309-320, 2018 01 28.
Artículo en Inglés | MEDLINE | ID: mdl-29194114

RESUMEN

OBJECTIVES: For both HIV-1 and hepatitis C virus (HCV), assessing the stringency of the transmission process is a scientific priority. Enumerations of transmitted/founder (TF) viruses have shown a strict transmission bottleneck in sexual transmission of HIV-1 and a wide range in the multiplicity of infection in HCV. Here, we aim to determine the stringency of parenteral transmission for HIV-1 and HCV in people who inject drugs (PWID). DESIGN: We used molecular sequencing and several complementary analyses to enumerate the TF HIV-1 and HCV variants in a well described cohort of PWID in Xinjiang, China. METHODS: We performed single genome sequencing of HIV-1 env and 5' half HCV genomes, then applied phylogenetic analysis and validated models of early virus diversification to enumerate TF viruses in 60 PWID. We used multivariate analysis to determine correlates of multivariant transmission (MVT). RESULTS: We generated 1070 env region sequences from 33 HIV-1 early infected individuals and 773 5' half region sequences from 27 HCV early infected individuals. We found rates of MVT of 39 and 54%, respectively, for HIV-1 and HCV, with a limited range in the number of TF viruses in both infections. Behavioural characteristics suggested high-risk injection practices and lower risk sexual practices; we did not find an association between any specific behaviours and MVT. CONCLUSION: MVT is frequent in parenteral transmission of both HIV-1 and HCV in Xinjiang PWID, indicating a less stringent transmission process than sexual transmission.


Asunto(s)
Transmisión de Enfermedad Infecciosa , Variación Genética , Infecciones por VIH/virología , VIH-1/clasificación , Hepacivirus/clasificación , Hepatitis C/virología , Abuso de Sustancias por Vía Intravenosa/complicaciones , Adulto , Pueblo Asiatico , China , Femenino , Genotipo , Infecciones por VIH/complicaciones , Infecciones por VIH/transmisión , VIH-1/genética , VIH-1/aislamiento & purificación , Hepacivirus/genética , Hepacivirus/aislamiento & purificación , Hepatitis C/complicaciones , Hepatitis C/transmisión , Humanos , Masculino , Filogenia , ARN Viral/genética , Análisis de Secuencia de ADN , Adulto Joven , Productos del Gen env del Virus de la Inmunodeficiencia Humana/genética
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