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      1586. Impact of Dolutegravir-based Regimen on Metabolic Syndrome and its Components in Adults with HIV in Care at Hospital Roosevelt in Guatemala City

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          Abstract

          Background

          Integrase inhibitors (INSTI) are associated with weight gain, elevated glucose and lipid changes. Use of the INSTI dolutegravir (DTG) is increasing in Latin America. We assessed the impact of DTG switch on Metabolic Syndrome (MetS) and its components in people with HIV (PWH) in Guatemala.

          Methods

          Participants with an HIV RNA < 1000 copies/ml on non-INSTI antiretroviral therapy (ART) for > 6 months who had a study visit between June 2019 and March 2020, and had complete data on MetS criteria were followed prospectively until May 2022. Those who switched to DTG-based regimen during follow up were compared to those who remained on a non-INSTI regimen. Switch participants were required to have remained on DTG for one year. We used the Latin American Diabetes Association criteria for MetS and cut-offs for waist circumference. Rates of MetS and its components were calculated at baseline and follow-up. Covariates included sex, residence, ethnicity, CD4 count, BMI, and ART. Significant covariates (p < 0.05) were included in multivariable logistic regression analyses.

          Results

          Of 258 participants included, 82% were on efavirenz-based regimens at baseline, 52% switched to DTG (median DTG exposure of 17.5 months, interquartile range [IQR] 14.7-21.7). Overall, 91.5% remained on the same ART backbone. The MetS rate was 29.5% at baseline, and there was no between-group difference in MetS and its components. The non-switch group had a greater proportion of females, indigenous ethnicity, and a higher BMI (Table 1). MetS rate was 39.5% at follow-up (+7.4% switch group vs +13% non-switch group; p=0.39). On multivariable analysis there was no association between DTG switch and MetS (aOR 0.93; IC 0.52,1.6; p=0.78). Participants that switched to DTG were less likely to meet hypertriglyceridemia criteria (aOR 0.53; IC 0.38, 0.90; p=0.02), and more likely to meet HDL cholesterol criteria (aOR 1.93; IC 1.1,3.3; p=0.02) (Table 2).

          Conclusion

          Overall, MetS increased substantially in the follow-up period in PWH in Guatemala. We found no association between DTG switch and increased MetS. Although hypertriglyceridemia improved following DTG-switch, the potential beneficial effect might be offset by a greater reduction in HDL cholesterol, highlighting the importance of examining individual components of MetS in PWH.

          Disclosures

          Carlos Mejia-Chew, MD, INSMED: Grant/Research Support|RevImmune: Grant/Research Support

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          Author and article information

          Contributors
          Journal
          Open Forum Infect Dis
          Open Forum Infect Dis
          ofid
          Open Forum Infectious Diseases
          Oxford University Press (US )
          2328-8957
          December 2023
          27 November 2023
          27 November 2023
          : 10
          : Suppl 2 , IDWeek 2023 Abstracts
          : ofad500.1421
          Affiliations
          Hospital Roosevelt , Guatemala City, Guatemala, Guatemala
          Hospital Roosevelt , Guatemala City, Guatemala, Guatemala
          Hospital Roosevelt , Guatemala City, Guatemala, Guatemala
          Washington University School of Medicine in St. Louis , St. Louis, Missouri
          Washington University in St. Louis , St. Louis, Missouri
          Hospital Roosevelt , Guatemala City, Guatemala, Guatemala
          Hospital Roosevelt , Guatemala City, Guatemala, Guatemala
          Hospital Roosevelt , Guatemala City, Guatemala, Guatemala
          Washington University in St Louis , St. Louis, Missouri
          Washington University School of Medicine in St. Louis , St. Louis, Missouri
          Author notes

          Session: 150. HIV: Treatment

          Friday, October 13, 2023: 12:15 PM

          Article
          ofad500.1421
          10.1093/ofid/ofad500.1421
          10677742
          17cf0eaf-2ef4-4f2f-abf9-f90aeae1bb13
          © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America.

          This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

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          AcademicSubjects/MED00290

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