Literature DB >> 8204773

Disease due to the Mycobacterium avium complex in patients with AIDS: epidemiology and clinical syndrome.

C A Benson1.   

Abstract

Infection due to the Mycobacterium avium complex (MAC) is the most common opportunistic disease of bacterial origin among patients with AIDS in the United States. The incidence of disseminated disease due to MAC (DMAC) has risen dramatically in recent years. The risk of developing DMAC increases as the CD4+ lymphocyte count declines to < 100/mm3. Preliminary analyses of several studies suggest that gender, racial or ethnic group, and individual risk factors for human immunodeficiency virus infection do not influence the incidence of DMAC but that prior Pneumocystis carinii pneumonia, the development of severe anemia, or the interruption of antiretroviral therapy may increase risk. Both the respiratory and the gastrointestinal tracts probably serve as portals of entry for MAC. Colonization may potentiate the risk of DMAC but does not always precede dissemination. Patients with AIDS and DMAC have a shorter duration of survival than do those with AIDS but without DMAC. While treatment for DMAC may extend survival, no well-controlled, prospective, randomized clinical trial has documented this point. Most patients with AIDS and DMAC have disseminated multiorgan disease; the most frequently described symptoms include fever, night sweats, weight loss or wasting, diarrhea, and abdominal pain. The most commonly identified laboratory abnormalities are anemia and elevated serum levels of alkaline phosphatase. Localized disease syndromes related to MAC infection occur less often.

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Year:  1994        PMID: 8204773     DOI: 10.1093/clinids/18.supplement_3.s218

Source DB:  PubMed          Journal:  Clin Infect Dis        ISSN: 1058-4838            Impact factor:   9.079


  25 in total

1.  Use of specific rRNA oligonucleotide probes for microscopic detection of Mycobacterium avium complex organisms in tissue.

Authors:  Allison L St Amand; Daniel N Frank; Mary Ann De Groote; Norman R Pace
Journal:  J Clin Microbiol       Date:  2005-04       Impact factor: 5.948

2.  Radiometric quantification of Mycobacterium avium complex.

Authors:  C J Haug; P Gaustad; F Müller
Journal:  Eur J Clin Microbiol Infect Dis       Date:  1998-06       Impact factor: 3.267

3.  Hemolysin as a virulence factor for systemic infection with isolates of Mycobacterium avium complex.

Authors:  J N Maslow; D Dawson; E A Carlin; S M Holland
Journal:  J Clin Microbiol       Date:  1999-02       Impact factor: 5.948

Review 4.  Epidemiology of infection by nontuberculous mycobacteria.

Authors:  J O Falkinham
Journal:  Clin Microbiol Rev       Date:  1996-04       Impact factor: 26.132

Review 5.  Epidemiological and clinical aspects of mycobacterial infections.

Authors:  M Opravil
Journal:  Infection       Date:  1997 Jan-Feb       Impact factor: 3.553

6.  Use of nucleic acid probes to identify mycobacteria directly from Difco ESP-Myco bottles.

Authors:  V J Labombardi; L Carter; S Massarella
Journal:  J Clin Microbiol       Date:  1997-04       Impact factor: 5.948

7.  Oligonucleotide (GTG)5 as an epidemiological tool in the study of nontuberculous mycobacteria.

Authors:  F J Cilliers; R M Warren; J H Hauman; I J Wiid; P D van Helden
Journal:  J Clin Microbiol       Date:  1997-06       Impact factor: 5.948

Review 8.  Pathology of non-Helicobacter pylori gastritis: extending the histopathologic horizons.

Authors:  Gregory Y Lauwers; Hiroshi Fujita; Koji Nagata; Michio Shimizu
Journal:  J Gastroenterol       Date:  2009-12-05       Impact factor: 7.527

9.  Endogenous interleukin-12 is involved in resistance of mice to Mycobacterium avium complex infection.

Authors:  B M Saunders; Y Zhan; C Cheers
Journal:  Infect Immun       Date:  1995-10       Impact factor: 3.441

10.  The combination of plasmid interleukin-12 with a single DNA vaccine is more effective than Mycobacterium bovis (bacille Calmette-Guèrin) in protecting against systemic Mycobacterim avium infection.

Authors:  Ela Martin; Arun T Kamath; Helen Briscoe; Warwick J Britton
Journal:  Immunology       Date:  2003-06       Impact factor: 7.397

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