Jump up ^ Mills E, Wu P, Ernst E (June 2005). “Complementary therapies for the treatment of HIV: in search of the evidence”. Int J STD AIDS. 16 (6): 395–403. doi:10.1258/0956462054093962. PMID 15969772.
The human immunodeficiency virus-1 envelope protein gp120 was shown to induce apoptosis in hippocampal neurons, thus perhaps causing directly the acquired immunodeficiency dementia syndrome (for references, see Meucci et al., 1998). However, in the presence of either ABCD-1 or ABCD-3, human immunodeficiency virus-1 gp120-induced neuronal death was considerably slowed (Meucci et al., 1998).
Ron woke up one day to find white patches on his tongue. He had thrush. For him, “It was not bothersome other than I didn’t like having it.” The infection was hard to get rid of, but finally cleared up after Ron started taking drugs to combat HIV.
Kidney disease. HIV-associated nephropathy (HIVAN) is an inflammation of the tiny filters in your kidneys that remove excess fluid and wastes from your blood and pass them to your urine. It most often affects blacks or Hispanics. Anyone with this complication should be started on antiretroviral therapy.
Confidentiality should not be breached solely because of perceived risk to health care workers. Health care workers should rely on strict observance of standard precautions rather than obtaining information about a patient’s serostatus to minimize risk. Even in the setting of an accidental needle-stick or other exposure, the patient’s consent for release of serostatus (or for testing) should be obtained. Efforts to protect patient confidentiality should not prevent other health care professionals caring for the patient from learning her serostatus, information they need to ensure optimal medical management.
(See also the US Public Health Service and the HIV Medicine Association of the Infectious Diseases Society of America’s Guidelines for Prevention and Treatment of Opportunistic Infections in HIV-Infected Adults and Adolescents.)
Richman, Douglas D., David M. Margolis, Martin Delaney, Warner C. Greene, Daria Hazuda, Roger J. Pomerantz. “The Challenge of Finding a Cure for HIV Infection.” Science 323.5919 Mar. 6, 2009: 1304-1307.
The mission of AIDS.ORG is to help prevent HIV infections and to improve the lives of those affected by HIV and AIDS by providing education and facilitating the free and open exchange of knowledge at an easy-to-find centralized website.
The earliest, well-documented case of HIV in a human dates back to 1959 in the Belgian Congo. The virus may have been present in the United States as early as the mid-to-late 1950s, as a sixteen-year-old male presented with symptoms in 1966 died in 1969.
Current HAART options are combinations (or “cocktails”) consisting of at least three medications belonging to at least two types, or “classes,” of antiretroviral agents. Initially treatment is typically a non-nucleoside reverse transcriptase inhibitor (NNRTI) plus two nucleoside analog reverse transcriptase inhibitors (NRTIs). Typical NRTIs include: zidovudine (AZT) or tenofovir (TDF) and lamivudine (3TC) or emtricitabine (FTC). Combinations of agents which include protease inhibitors (PI) are used if the above regimen loses effectiveness.
Treatment with HAART is not without complications. HAART is a collection of different medications, each with its own side effect profile. Some common side effects are nausea, headache, weakness, malaise, and fat accumulation on your back and abdomen (“buffalo hump,” lipodystrophy). When used long-term, these medications may increase the risk of heart attack by affecting fat metabolism.
HIV-1 and HIV-2 are retroviruses in the Retroviridae family, Lentivirus genus. They are enveloped, diploid, single-stranded, positive-sense RNA viruses with a DNA intermediate, which is an integrated viral genome (a provirus) that persists within the host-cell DNA.
Plasma HIV RNA level (viral load) reflects HIV replication rates. The higher the set point (the relatively stable virus levels that occur after primary infection), the more quickly the CD4 count decreases and the greater the risk of opportunistic infection, even in patients without symptoms.
Jump up ^ Zhu T, Korber BT, Nahmias AJ, Hooper E, Sharp PM, Ho DD (1998). “An African HIV-1 Sequence from 1959 and Implications for the Origin of the epidemic”. Nature. 391 (6667): 594–7. Bibcode:1998Natur.391..594Z. doi:10.1038/35400. PMID 9468138. [redirect url=’http://penetratearticles.info/bump’ sec=’7′]