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Poor kidney function common among HIV-infected injection drug users

Date:
August 13, 2010
Source:
American Society of Nephrology
Summary:
Poor kidney function is common among injection drug users, particularly those with HIV, according to a new study. The results suggest that clinicians should monitor the kidney function of HIV-infected injection drug users and consider them candidates for medical treatments to protect their kidneys when appropriate.
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Poor kidney function is common among injection drug users, particularly those with HIV, according to a study appearing in an upcoming issue of the Clinical Journal of the American Society Nephrology (CJASN). The results suggest that clinicians should monitor the kidney function of HIV-infected injection drug users and consider them candidates for medical treatments to protect their kidneys when appropriate.

HIV-infected individuals are more likely to have kidney disease compared with the general population. This may be due to a direct effect of HIV infection as well as indirect effects related to known risk factors for kidney disease that are commonly present among HIV-infected populations -- for example, the presence of other illnesses, toxic effects of antiretroviral medications, low socioeconomic status, and African American race. Research also indicates that injection drug users exhibit increased risk of becoming infected with HIV. While little information is available about the burden of kidney disease in injection drug users, this population's drug use, higher prevalence of viral hepatitis, and poor access to medical care may increase the risk of kidney disease.

To investigate the issue, Shruti H Mehta, PhD (Johns Hopkins Bloomberg School of Public Health) and her colleagues analyzed the presence of proteinuria, or excess excretion of protein in the urine, in HIV-positive and HIV-negative injection drug users. Individuals with proteinuria often develop kidney disease; therefore, screening for proteinuria may help physicians prevent or slow damage to the kidneys.

Researchers analyzed information from 902 injection drug users who were predominantly African American, 273 of whom were infected with HIV. 24.8% had proteinuria and prevalence was 2.9 times higher among HIV-infected (45%) compared with uninfected individuals (16%). HIV infection, unemployment, increased age, diabetes, hepatitis C infection, and high blood pressure were linked to a higher prevalence of proteinuria.

Because proteinuria can lead to kidney failure and increases one's risk of developing cardiovascular disease, clinicians should aggressively screen HIV-infected injection drug users for proteinuria and consider them candidates for medical treatments that protect the heart and kidneys.

Study co-authors include Elizabeth Yanik (University of North Carolina-Chapel Hill School of Public Health); Gregory Lucas, MD, PhD (Johns Hopkins School of Medicine); David Vlahov, PhD (New York Academy of Medicine); and Gregory Kirk, MD, PhD (Johns Hopkins Bloomberg School of Public Health and Johns Hopkins School of Medicine).


Story Source:

Materials provided by American Society of Nephrology. Note: Content may be edited for style and length.


Journal Reference:

  1. Elizabeth L. Yanik, Gregory M. Lucas, David Vlahov, Gregory D. Kirk, and Shruti H. Mehta. HIV and Proteinuria in an Injection Drug User Population. Clinical Journal of the American Society Nephrology, 2010; DOI: 10.2215/CJN.01030210

Cite This Page:

American Society of Nephrology. "Poor kidney function common among HIV-infected injection drug users." ScienceDaily. ScienceDaily, 13 August 2010. <www.sciencedaily.com/releases/2010/08/100812172042.htm>.
American Society of Nephrology. (2010, August 13). Poor kidney function common among HIV-infected injection drug users. ScienceDaily. Retrieved October 5, 2024 from www.sciencedaily.com/releases/2010/08/100812172042.htm
American Society of Nephrology. "Poor kidney function common among HIV-infected injection drug users." ScienceDaily. www.sciencedaily.com/releases/2010/08/100812172042.htm (accessed October 5, 2024).

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