Brief Report: Zinc Supplementation and Inflammation in Treated HIV

Sahera Dirajlal-Fargo, Jiao Yu, Manjusha Kulkarni, Abdus Sattar, Nicholas Funderburg, Hope Barkoukis, Grace A. McComsey*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

11 Scopus citations

Abstract

Objective:In this study, we explored the effect of zinc supplementation on markers of inflammation and monocyte activation in antiretroviral therapy-treated HIV infection.Methods:This is a phase I open-labeled randomized double-arm study, exploring the efficacy and safety of zinc supplementation on inflammation in ≥18-year-old people living with HIV in the US, on stable antiretroviral therapy and with zinc levels ≤75 μg/dL in the last 60 days. Patients were randomized 1:1 to zinc gluconate capsules at a dose of 45 mg (low-dose), or 90 mg (high-dose) elemental zinc daily for 16 weeks. We assessed inflammatory and gut integrity biomarkers at baseline and 16 weeks.Results:Overall, a total of 52 participants were enrolled (25 participants in the low-dose arm and 27 participants in the high-dose arm). Median (Interquartile range) age was 49 (38, 60) years, 77% were men and 73% were African Americans. At baseline, median zinc levels were 73 (64, 86) μg/dL. Median circulating zinc levels increased to 91 μg/dL in the low-dose arm and to 100 μg/dL in the high-dose arm. Overall, 48%-60% of participants experienced a reduction in biomarkers levels. The margin of reduction ranged between 8% and 21%. This change was meaningful with large effect size (Cohen D ranging from 5 to 19).Conclusions:In this pilot study, we found that zinc supplementation is effective at increasing circulating zinc levels. In addition, our findings provide novel data suggesting that zinc can affect a biological signature in people living with HIV and modulate biomarkers associated with clinical comorbidities.

Original languageEnglish (US)
Pages (from-to)275-280
Number of pages6
JournalJournal of Acquired Immune Deficiency Syndromes
Volume82
Issue number3
DOIs
StatePublished - Nov 1 2019

Funding

Supported by a grant from NCCIH (AT009153) to G.A.M. Additional support was provided by the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) to S.D.-F (K23HD088295-01A1).

Keywords

  • HIV
  • gut integrity
  • immune activation
  • inflammation
  • morbidity
  • zinc

ASJC Scopus subject areas

  • Infectious Diseases
  • Pharmacology (medical)

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