Anemia is common during human immunodeficiency virus (HIV) infection and is associated with increased HIV disease progression and higher mortality. Consequences of anemia include fatigue, a decreased sense of well-being, and a greater need for expensive recombinant human erythropoietin therapy, transfusions, and hospitalizations. Our studies show that the cumulative incidence of anemia is 100 percent among HIV-infected female injection drug users, and that iron deficiency anemia accounts for about half of the anemia. Iron deficiency is a major neglected problem of women, and no progress has been made in reducing the prevalence of iron deficiency among women in the U.S. over the last 30 years. Although iron supplementation can be used to prevent and treat iron deficiency anemia, concerns have been raised since iron supplementation and iron overload have been associated with increased HIV disease progression, higher mortality, and progression of hepatitis C (HCV) infection. These concerns have led to a dilemma about the use of iron supplements for iron deficiency and anemia in women with HIV and HCV. The prevalence of HCV is especially high among injection drug users in urban settings. Research is needed to determine whether the benefits of iron supplementation in this population outweigh the potential risks.
Our specific aims are to determine whether a multivitamin and iron supplement can effectively reduce iron deficiency and anemia among HIV-positive and HIV-negative female injection drug users without worsening HIV or HCV infection. To address these aims, we propose to conduct a randomized controlled clinical trial of daily multivitamin and iron supplementation for 600 female injection drug users. Outcome measures include hemoglobin, indicators of HIV and HCV disease severity, and iron status, and the trial will be monitored by a data and safety monitoring committee. If the proposed trial shows that a multivitamin and iron supplement reduces anemia and does not worsen HIV or hepatitis C infection, the findings could be used to establish evidence-based guidelines for the prevention and/or reduction of anemia among women in the U.S. and elsewhere.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Project (R01)
Project #
3R01DA015022-03S1
Application #
6804768
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Khalsa, Jagjitsingh H
Project Start
2001-09-30
Project End
2005-07-31
Budget Start
2003-09-30
Budget End
2004-07-31
Support Year
3
Fiscal Year
2003
Total Cost
$102,448
Indirect Cost
Name
Johns Hopkins University
Department
Ophthalmology
Type
Schools of Medicine
DUNS #
001910777
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Semba, Richard D; Ricketts, Erin P; Mehta, Shruti et al. (2007) Effect of micronutrients and iron supplementation on hemoglobin, iron status, and plasma hepatitis C and HIV RNA levels in female injection drug users: a controlled clinical trial. J Acquir Immune Defic Syndr 45:298-303
Semba, Richard D; Ricketts, Erin P; Mehta, Shruti F et al. (2007) Adherence and retention of female injection drug users in a phase III clinical trial in inner city Baltimore. Am J Drug Alcohol Abuse 33:71-80
Dancheck, Barbara; Tang, Alice M; Thomas, Ann M et al. (2005) Injection drug use is an independent risk factor for iron deficiency and iron deficiency anemia among HIV-seropositive and HIV-seronegative women. J Acquir Immune Defic Syndr 40:198-201
Semba, Richard D; Martin, Barbara K; Kempen, John H et al. (2005) The impact of anemia on energy and physical functioning in individuals with AIDS. Arch Intern Med 165:2229-36
Kwong, Wilson T; Friello, Phyllis; Semba, Richard D (2004) Interactions between iron deficiency and lead poisoning: epidemiology and pathogenesis. Sci Total Environ 330:21-37
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