Journal of Gastroenterology and Hepatology · 2007 · 30 citations · 16 references
MedicineInfectious DiseasesInternal MedicineGastroenterologyImmunology Of Infectious DiseasesInfectious Disease EpidemiologyAntiretroviral TherapyGastrointestinal EndoscopyImmunodeficiency DisordersPeptic Ulcer DiseaseCd4 Cell Count MonitoringCd4 Positive T CellsEarly Antiretroviral TherapyEpigastric Pain SyndromeGastrointestinal MucosaHighly Active Antiretroviral TherapyHiv Antiretroviral TherapyHiv-associated Immunosuppression
BACKGROUND AND AIM: Upper gastrointestinal symptoms, mainly dyspepsia, are common adverse effects in patients under highly active antiretroviral therapy (HAART). Whether it is worthwhile to perform endoscopy early in their treatment is a matter of debate. We have done a prospective study of the prevalence and the etiology of endoscopic lesions in a large cohort of dyspeptic adult HIV-infected patients under HAART, according to their immunological status. METHODS: 528 (334 men and 194 women, mean age 38) HIV-infected patients under HAART with epigastric pain and/or nausea and vomiting underwent upper endoscopy. Patients were classified in two groups, according to CD4 cells counting (>200 cells/mm(3) or < or =200 cells/mm(3)). Gastric and duodenal biopsies were taken from normal mucosa and any lesion found. RESULTS: Gastric mucosa alterations were seen in 61.74% of patients (40.71% erythema, 18.38% erosion and 2.65% ulcer). Duodenum mucosa alterations were seen in 25.37% of patients, mainly erosions (19.50%) and ulcer (3.59%). There was no difference in endoscopic findings according to CD4 cell count groups. Chronic active gastritis was shown in 459 patients (86.93%). H. pylori infection was seen in 32.38%, and it was more prevalent in the group with CD4 > 200 (p < 0.01). Opportunistic infections and malignancies were seen exclusively in patients with CD4 < or = 200. CONCLUSIONS: Most of the endoscopic lesions in dyspeptic HIV-infected patients under HAART were not related to AIDS. Upper endoscopy was more helpful in dictating clinical treatment in patients with low CD4 counts (< or =200) and should be done earlier in this group.
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Schlomo Staszewski, Javier O Morales-Ramirez, Karen T. Tashima et al. · New England Journal of Medicine · 1999 · 1K citations · Full text
Antonella d’Arminio Monforte, Alessandro Cozzi‐Lepri, Giovanni Rezza et al. · AIDS · 2000 · 560 citations
Correction: The role of interleukin-1 polymorphisms in the pathogenesis of gastric cancer
Emad El‐Omar, Mary Carrington, Wong‐Ho Chow et al. · Nature · 2001 · 218 citations · Full text
Life Sciences, Genetics, Immunology +14