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2.
Clinics ; 66(7): 1171-1175, 2011. tab
Article in English | LILACS | ID: lil-596903

ABSTRACT

OBJECTIVE: Immunosuppressed patients are at risk of microsporidiosis, and this parasitosis has an increased rate of dissemination in this population. Our objective was to evaluate the presence of microsporidiosis and other intestinal parasites in rheumatic disease patients undergoing anti-tumor necrosis factor/disease-modifying anti-rheumatic drug treatment. METHODS: Ninety-eight patients (47 with rheumatoid arthritis, 31 with ankylosing spondylitis and 11 with psoriatic arthritis) and 92 healthy control patients were enrolled in the study. Three stool samples and cultures were collected from each subject. RESULTS: The frequency of microsporidia was significantly higher in rheumatic disease patients than in control subjects (36 vs. 4 percent, respectively; p<0.0001), as well as in those with rheumatic diseases (32 vs. 4 percent, respectively; p<0.0001), ankylosing spondylitis (45 vs. 4 percent, respectively; p<0.0001) and psoriatic arthritis (40 vs. 4 percent, respectively; p<0.0001), despite a similar social-economic class distribution in both the patient and control groups (p = 0.1153). Of note, concomitant fecal leukocytes were observed in the majority of the microsporidia-positive patients (79.5 percent). Approximately 80 percent of the patients had gastrointestinal symptoms, such as diarrhea (26 percent), abdominal pain (31 percent) and weight loss (5 percent), although the frequencies of these symptoms were comparable in patients with and without this infection (p>0.05). Rheumatoid arthritis, ankylosing spondylitis and psoriatic arthritis disease activity parameters were comparable in both groups (p>0.05). The duration of anti-tumor necrosis factor/disease-modifying anti-rheumatic drugs and glucocorticoid use were also similar in both groups. CONCLUSION: We have documented that microsporidiosis with intestinal mucosa disruption is frequent in patients undergoing concomitant anti-tumor necrosis factor/disease-modifying anti-rheumatic drug therapy. Impaired host defenses due to the combination of the underlying disease and the immunosuppressive therapy is the most likely explanation for this finding, and this increased susceptibility reinforces the need for the investigation of microsporidia and implementation of treatment strategies in this population.


Subject(s)
Adult , Female , Humans , Male , Middle Aged , Antirheumatic Agents/adverse effects , Intestinal Diseases/microbiology , Microsporidiosis/immunology , Rheumatic Diseases/drug therapy , Tumor Necrosis Factor-alpha/antagonists & inhibitors , Case-Control Studies , Drug Therapy, Combination/adverse effects , Immunocompromised Host/immunology , Immunosuppressive Agents/adverse effects , Risk Factors , Rheumatic Diseases/immunology , Socioeconomic Factors , Statistics, Nonparametric
3.
Rev. latinoam. microbiol ; 38(2): 151-66, abr.-jun. 1996. ilus, tab
Article in Spanish | LILACS | ID: lil-187857

ABSTRACT

Los protozoos del orden Microsporida se han considerado como causantes de diversas patologías en pacientes con inmunodeficiencias severas. Aparentemente se trasmiten al humano por fecalismo, pero también se ha considerado la vía respiratoria. Los más afectados son adultos jóvenes del sexo masculino infectados con virus de la inmunodeficiencia humana. Entre los géneros más importantes se encuentran: Enterocytozoon, Encephalitozoom, Septata, Nosema y Pleistophora. Aún existen discrepancias en cuanto a la biología del parásito y poco se conoce acerca de su comportamiento dentro del humano. Se concluye que con el Advenimiento del SIDA, se están presentando múltiples nosologías por oportunistas que anteriormente no se consideraban como infecciones humanas. Este trabajo es una revisión de lo publicado de 1959 a 1995, relativo a aspectos epidemiológicos, clínicos, diagnósticos y terapéuticos


Subject(s)
Adult , Humans , Male , AIDS-Related Opportunistic Infections/etiology , AIDS-Related Opportunistic Infections/parasitology , Microsporida/growth & development , Microsporida/pathogenicity , Microsporidiosis/drug therapy , Microsporidiosis/etiology , Microsporidiosis/immunology , Microsporidiosis/transmission , Acquired Immunodeficiency Syndrome/parasitology
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