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1.
Mol Genet Metab ; 110(3): 411-3, 2013 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-24063868

RESUMEN

We hypothesize that abnormal fat distribution, a common feature of PMM2-CDG, is associated with abnormal perinatal hormone regulation. We assessed 32 cases with PMM2-CDG, for the comorbidity of hypoglycemia/hyperinsulinism and fat pads. Ninety percent of patients with hypoketotic hypoglycemia and/or hyperinsulinism had abnormal fat distribution, while normoglycemic patients showed this feature in 50% of the cases. This statistically significant difference suggests an etiological role of the insulin receptor in developing abnormal fat distribution in PMM2-CDG.


Asunto(s)
Tejido Adiposo/patología , Adiposidad , Trastornos Congénitos de Glicosilación/patología , Glucemia , Trastornos Congénitos de Glicosilación/metabolismo , Humanos , Insulina/sangre
2.
Int J Antimicrob Agents ; 33(1): 21-6, 2009 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-18774697

RESUMEN

Since caspofungin inhibits fungal cell wall beta-glucan synthesis and the fungal cell wall plays an important role in the recognition of Candida by phagocytic cells, we studied phagocytosis in the presence of caspofungin. The aim of this work was to investigate the effect of pre-treatment of Candida parapsilosis with caspofungin on phagocytic mechanisms (opsonisation, oxidative burst, phagocytosis and killing). C. parapsilosis grown in the presence of caspofungin at concentrations above the minimal inhibitory concentration (MIC) were more difficult to opsonise and to phagocytose. C. parapsilosis exposed to any concentration of caspofungin below and above the MIC was more difficult to kill. Caspofungin-treated C. parapsilosis impaired the oxidative burst. Overall, it appears that caspofungin treatment of C. parapsilosis alters the capacity of polymorphonuclear leukocytes to phagocytose and delays killing of the organism. This may allow C. parapsilosis to persist in tissues.


Asunto(s)
Antifúngicos/farmacología , Candida/efectos de los fármacos , Candida/crecimiento & desarrollo , Equinocandinas/farmacología , Neutrófilos/efectos de los fármacos , Neutrófilos/inmunología , Fagocitosis/efectos de los fármacos , Candida/clasificación , Caspofungina , Farmacorresistencia Fúngica , Humanos , Inmunidad Innata/efectos de los fármacos , Lipopéptidos , Pruebas de Sensibilidad Microbiana , Proteínas Opsoninas/metabolismo , Estallido Respiratorio/efectos de los fármacos
3.
Int J Antimicrob Agents ; 23(5): 506-9, 2004 May.
Artículo en Inglés | MEDLINE | ID: mdl-15120732

RESUMEN

Management of urinary tract infections (UTI) in Central America and especially Nicaragua, is complicated by the lack of knowledge about the antibiotic resistance of uropathogens. We conducted a prevalence study to gain more insight into the aetiology, bacterial resistance and risk factors for symptomatic UTI in the region of León, Nicaragua. In 2002, all consecutive patients with UTI symptoms and pyuria >/=10 WBC/hpf were admitted to the study. Positive cultures from midstream urine specimens were defined as >/=10(5) cfu/ml of a single uropathogen. Susceptibility tests were performed with disc diffusion tests using the Kirby-Bauer method and broth microdilution using National Committee for Clinical Laboratory Standards criteria both in León and a reference laboratory in Utrecht. A positive culture was present in 62 of 208 study subjects (30%). Escherichia coli (56%), Klebsiella spp. (18%) and Enterobacter spp. (11%) were the most frequent pathogens isolated. Presence of cystocele, incontinence and increasing age were risk factors for bacterial UTI. E. coli was least resistant to ceftriaxone, amikacin and nitrofurantoin (>90% susceptible). We observed high resistance rates in E. coli to amoxicillin (82%, MIC(90) 128 mg/l), trimethoprim-sulphamethoxazole (TMP-SMX) (64%, MIC(90) 32 mg/l), cephalothin (58%, MIC(90), 32 mg/l), ciprofloxacin (30%; MIC(90), 32 mg/l), amoxicillin/clavulanate (21%, MIC(90) 8 mg/l) and gentamicin (12%, MIC(90) 2 mg/l). Our results suggests that community acquired uropathogens in Nicaragua are highly resistant to many antimicrobial agents. The use of amoxicillin, trimethoprim-sulphamethoxazole and cephalothin against uropathogens needs to be reconsidered. High quinolone resistance rates among E. coli in Nicaragua gives cause for great concern.


Asunto(s)
Antibacterianos/farmacología , Bacterias/efectos de los fármacos , Bacterias/aislamiento & purificación , Infecciones Urinarias/microbiología , Adulto , Amoxicilina/farmacología , Amoxicilina/uso terapéutico , Cefalotina/farmacología , Cefalotina/uso terapéutico , Combinación de Medicamentos , Farmacorresistencia Bacteriana , Enterobacter/efectos de los fármacos , Enterobacter/aislamiento & purificación , Escherichia coli/efectos de los fármacos , Escherichia coli/aislamiento & purificación , Femenino , Humanos , Klebsiella/efectos de los fármacos , Klebsiella/aislamiento & purificación , Masculino , Pruebas de Sensibilidad Microbiana , Nicaragua , Piuria/microbiología , Quinolonas/farmacología , Quinolonas/uso terapéutico , Factores de Riesgo , Sulfametizol/farmacología , Sulfametizol/uso terapéutico , Trimetoprim/farmacología , Trimetoprim/uso terapéutico , Enfermedades de la Vejiga Urinaria , Incontinencia Urinaria , Infecciones Urinarias/tratamiento farmacológico , Infecciones Urinarias/epidemiología , Orina/microbiología
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