José M. Arribas
University of Oviedo
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Clinical Infectious Diseases | 2004
Victor Asensi; Eustaquio Martín Roces; José A. Carton; Julio Collazos; José A. Maradona; Ángeles Alonso; Marifé Medina; Jesús M. Aburto; Esteban Martínez; Carmen Rojo; Enrique Bustillo; Cristina Fernández; José M. Arribas
Echographically measured thicknesses of perirenal and subcutaneous fat, as well as serum metabolic and anthropometric parameters, were evaluated in 74 human immunodeficiency virus-infected patients receiving highly active antiretroviral therapy (HAART), 22 of whom were HAART-naive at baseline, who were followed-up for 27 months to detect predictive factors of lipodystrophy. Perirenal fat diameter (PRFD) at baseline differed in HAART-naive and HAART-experienced patients (P<.001), and it was the best predictor of lipodystrophy changes after 12 months of follow-up in the HAART-naive patients (hazard ratio, 7.34; 95% confidence interval, 1.18-45.49; P=.032). In addition, HAART-experienced patients in whom lipodystrophy improved had thinner baseline perirenal fat than those in whom lipodystrophy did not improve (P=.04). A PRFD of >2.6 mm at baseline or >4.9 mm during receipt of HAART suggested lipodystrophy predisposition. PRFD correlated significantly with other metabolic and anthropometric parameters. Echographically measured PRFD is associated with lipodystrophy and could be used as an early predictor of this syndrome in treatment-naive patients starting HAART.
American Journal of Medical Genetics Part A | 2003
Victor Asensi; Victoria Alvarez; Eulalia Valle; Alvaro Meana; Joshua Fierer; Eliecer Coto; José A. Carton; José A. Maradona; Jose Paz; Maria Angeles Dieguez; Belén de la Fuente; Alfonso Moreno; Silvino Rubio; Maria José Tuya; Julián Sarasúa; Sara Llames; José M. Arribas
As osteomyelitis (OM) induces the synthesis of inflammatory cytokines and IL‐1 mediates bone resorption by osteoclasts we determined if there is an association between certain common polymorphisms of the genes encoding proinflammatory cytokines (IL‐1α and β, IL‐6, TNF‐α) and OM in adults. The IL‐1α (− 889) TT genotype was significantly more frequent among 52 OM patients than in 109 healthy controls (13/52, [25.0%] vs. 9/109, [8.3%], P = 0.0081, χ2 = 7.01, OR = 3.7, 95% CI, 1.35–10.34). Patients who were homozygous for the T allele were younger than the rest of the OM patients (mean age 35.7 ± 11.5 vs. 58.1 ± 18.6 years, P = 0.001). IL‐1β TT (+ 3953) polymorphism was also more frequent in OM patients (P = 0.014, χ2 = 5.12, OR = 5.1, 95% CI, 1.21–52.14), but IL‐1β is in linkage disequilibrium with the IL‐1α *T (P < 0.001). Route of infection, chronicity of the infection, type of microorganism isolated, and frequency of relapses were similar in patients with and without the IL‐1α TT genotype. There were no associations between OM and polymorphisms of other cytokines genes. IL‐1α serum levels were significantly increased in all the OM patients independently of their IL‐1 genotype compared to the controls (P = 0.021). Although IL‐1α serum levels were not significantly higher in patients with the IL‐1α (− 889) polymorphism, this does not exclude a difference in production of IL‐1α by osteoclasts or other inflammatory cells at the site of infection.
Infection | 2000
Victor Asensi; L. Tricas; Alvaro Meana; D. Roos; José A. Carton; José A. Maradona; M.F. Fresno; Eulalia Valle; Joshua Fierer; José M. Arribas
SummaryWe report a rare case of a male patient without known immunodeficiency consecutively diagnosed with visceral leishmaniasis, brain abscess and cavitating pneumonia in the 3rd decade of life. Chronic granulomatous disease (CGD) was diagnosed by a nitroblue tetrazolium test. A p47-phox mutation of the NADPH oxidase of the leukocytes was suspected by immunoblotting and confirmed by DNA analysis. The patient was homozygous for this mutation while his mother and sister were heterozygous asymptomatic carriers. After the CGD diagnosis the patient started a chronic prophylactic regimen with subcutaneous interferon-γ (0.05 mg/m2 of body surface/three times a week), and oral trimethoprim-sulfamethoxazole and itraconazole (both at 5 mg/kg/day) with no subsequent infections after 12 months of follow-up.
Infection | 2002
Victor Asensi; M. Alvarez; José A. Carton; M. Lago; José A. Maradona; J.M. Asensi; José M. Arribas
Eikenella corrodens is a facultatively anaerobic gramnegative rod that colonizes the oral cavity and very rarely produces central nervous system (CNS) infections. Frontal lobe abscesses are occasionally associated with a dental source of infection. We report a case of an adult man with overzealous dental cleaning habits who developed a right frontal brain abscess caused by E. corrodens. He underwent neurosurgical drainage of the pus and was successfully treated with imipenem 4 g/iv/day for 4 weeks with no complications. Repeated periodontal trauma could explain the Eikenella brain abscess in this case.
Current Microbiology | 1997
Victor Asensi; Francisco Parra; Joshua Fierer; Eulalia Valle; Carmen Bordallo; Paz Suárez Rendueles; Santiago Gascón; José A. Carton; José A. Maradona; José M. Arribas
Abstract.Bacillus subtilis is a ubiquitous soil bacterium used for measuring the β-lysin activity and in other bioassays. We observed a complete bactericidal effect of ADP on B. subtilis at concentrations of 50–100 μM at pH values <5.5, which disappeared at pH values above 6. The effect was also found for acetic acid at concentrations >17.4 μM and similar pH values. ATP, adenosine, and HCl were not bactericidal. We used BCECF-AM, a pH-sensitive probe, and found that the killing of B. subtilis was due to a change in the intracellular pH caused by the passage across the cell membrane of these weak organic acids when incubated with B. subtilis at pH values near the pK. More experiments are needed to determine the biological meaning of these in vitro findings.
JAMA Internal Medicine | 1987
José A. Carton; José A. Maradona; José M. Arribas
Journal of Antimicrobial Chemotherapy | 1996
Victor Asensi; José A. Carton; José A. Maradona; José María Asensi; Francisco Pérez; Pedro Redondo; Antonio García López; José M. Arribas
Clinical Infectious Diseases | 1993
Victor Asensi; José A. Carton; José A. Maradona; María de Oña; José M. Arribas
Medicina Clinica | 1999
Víctor Asensi; José A. Carton; José A. Maradona; María de Oña; S. Melón; Eustaquio R Martín-Roces; José María Asensi; José M. Arribas
Medicina Clinica | 1988
José A. Carton; García-Velasco G; José A. Maradona; Pérez F; Asensi; José M. Arribas