Incidence of metabolic syndrome in people with HIV who start dolutegravir based-regimen compared with bictegravir based-regimen after 48 weeks
Objective:Evidence suggests that patients initiating a second-generation integrase strand transfer inhibitors (INSTI)-based regimen may have a higher risk of developing metabolic syndrome (MetS) compared to those on other antiretroviral classes. This study aimed to describe the incidence of MetS at...
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Published in | AIDS (London) Vol. 39; no. 12; pp. 1731 - 1738 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Hagerstown, MD
Lippincott Williams & Wilkins
01.10.2025
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Subjects | |
Online Access | Get full text |
ISSN | 0269-9370 1473-5571 |
DOI | 10.1097/QAD.0000000000004259 |
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Abstract | Objective:Evidence suggests that patients initiating a second-generation integrase strand transfer inhibitors (INSTI)-based regimen may have a higher risk of developing metabolic syndrome (MetS) compared to those on other antiretroviral classes. This study aimed to describe the incidence of MetS at 48 weeks, based on ATP III criteria, in people with HIV (PWH) who started antiretroviral therapy (ART) with a DTG/ABC/3TC-based regimen compared to those receiving a BIC/TAF/FTC-based regimen.Design:A randomized, open-label clinical trial was conducted in PWH with no prior exposure to ART.Methods:Participants were randomized to receive either bictegravir/alafenamide tenofovir/emtricitabine (BIC/TAF/FTC) or dolutegravir/abacavir/lamivudine (DTG/ABC/3TC). Anthropometric measurements, including weight, height, blood pressure, waist circumference, bioelectrical impedance analysis, and visceral fat assessment via ultrasonography, were performed at baseline, 24 weeks, and 48 weeks. Metabolic parameters were evaluated at each visit.Results:Out of 378 subjects, 311 provided informed consent and were included. Of these, 276 completed 48 weeks of follow-up. The incidence of MetS was 6 (3.9%) and 10 (6.3%) in BIC/TAF/FTC and DTG/ABC/3TC arms, respectively, with no significant difference between groups. In the BIC/TAF/FTC group, 24 patients (9%) experienced a weight gain of ≥10%, compared to 16 patients (6%) in the DTG/ABC/3TC group (P = 0.72). Risk factors for MetS were age ≥40 years old, baseline BMI ≥25 kg/m2, and baseline visceral fat ≥5 cm prior to ART initiation.Conclusion:Incidence of MetS among PWH receiving an INSTI-based regimen was high, with no difference between BIC/TAF/FTC and DTG/ABC/3TC groups. Age, overweight and elevated visceral fat at baseline were all associated with MetS. |
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AbstractList | Evidence suggests that patients initiating a second-generation integrase strand transfer inhibitors (INSTI)-based regimen may have a higher risk of developing metabolic syndrome (MetS) compared to those on other antiretroviral classes. This study aimed to describe the incidence of MetS at 48 weeks, based on ATP III criteria, in people with HIV (PWH) who started antiretroviral therapy (ART) with a DTG/ABC/3TC-based regimen compared to those receiving a BIC/TAF/FTC-based regimen.
A randomized, open-label clinical trial was conducted in PWH with no prior exposure to ART.
Participants were randomized to receive either bictegravir/alafenamide tenofovir/emtricitabine (BIC/TAF/FTC) or dolutegravir/abacavir/lamivudine (DTG/ABC/3TC). Anthropometric measurements, including weight, height, blood pressure, waist circumference, bioelectrical impedance analysis, and visceral fat assessment via ultrasonography, were performed at baseline, 24 weeks, and 48 weeks. Metabolic parameters were evaluated at each visit.
Out of 378 subjects, 311 provided informed consent and were included. Of these, 276 completed 48 weeks of follow-up. The incidence of MetS was 6 (3.9%) and 10 (6.3%) in BIC/TAF/FTC and DTG/ABC/3TC arms, respectively, with no significant difference between groups. In the BIC/TAF/FTC group, 24 patients (9%) experienced a weight gain of ≥10%, compared to 16 patients (6%) in the DTG/ABC/3TC group ( P = 0.72). Risk factors for MetS were age ≥40 years old, baseline BMI ≥25 kg/m 2 , and baseline visceral fat ≥5 cm prior to ART initiation.
Incidence of MetS among PWH receiving an INSTI-based regimen was high, with no difference between BIC/TAF/FTC and DTG/ABC/3TC groups. Age, overweight and elevated visceral fat at baseline were all associated with MetS. Objective:Evidence suggests that patients initiating a second-generation integrase strand transfer inhibitors (INSTI)-based regimen may have a higher risk of developing metabolic syndrome (MetS) compared to those on other antiretroviral classes. This study aimed to describe the incidence of MetS at 48 weeks, based on ATP III criteria, in people with HIV (PWH) who started antiretroviral therapy (ART) with a DTG/ABC/3TC-based regimen compared to those receiving a BIC/TAF/FTC-based regimen.Design:A randomized, open-label clinical trial was conducted in PWH with no prior exposure to ART.Methods:Participants were randomized to receive either bictegravir/alafenamide tenofovir/emtricitabine (BIC/TAF/FTC) or dolutegravir/abacavir/lamivudine (DTG/ABC/3TC). Anthropometric measurements, including weight, height, blood pressure, waist circumference, bioelectrical impedance analysis, and visceral fat assessment via ultrasonography, were performed at baseline, 24 weeks, and 48 weeks. Metabolic parameters were evaluated at each visit.Results:Out of 378 subjects, 311 provided informed consent and were included. Of these, 276 completed 48 weeks of follow-up. The incidence of MetS was 6 (3.9%) and 10 (6.3%) in BIC/TAF/FTC and DTG/ABC/3TC arms, respectively, with no significant difference between groups. In the BIC/TAF/FTC group, 24 patients (9%) experienced a weight gain of ≥10%, compared to 16 patients (6%) in the DTG/ABC/3TC group (P = 0.72). Risk factors for MetS were age ≥40 years old, baseline BMI ≥25 kg/m2, and baseline visceral fat ≥5 cm prior to ART initiation.Conclusion:Incidence of MetS among PWH receiving an INSTI-based regimen was high, with no difference between BIC/TAF/FTC and DTG/ABC/3TC groups. Age, overweight and elevated visceral fat at baseline were all associated with MetS. |
Author | Salinas Velázquez, Gloria Elizabeth Mata Marín, José Antonio Meneses Cisneros, Betzahida Cano Díaz, Ana Luz Pompa Mera, Ericka Gaytán Martínez, Jesús Enrique Rodríguez Evaristo, Mara Soraya Triana González, Salma Chaparro Sánchez, Alberto |
Author_xml | – sequence: 1 givenname: José Antonio surname: Mata Marín fullname: Mata Marín, José Antonio – sequence: 2 givenname: Mara Soraya surname: Rodríguez Evaristo fullname: Rodríguez Evaristo, Mara Soraya – sequence: 3 givenname: Ana Luz surname: Cano Díaz fullname: Cano Díaz, Ana Luz – sequence: 4 givenname: Gloria Elizabeth surname: Salinas Velázquez fullname: Salinas Velázquez, Gloria Elizabeth – sequence: 5 givenname: Salma surname: Triana González fullname: Triana González, Salma – sequence: 6 givenname: Alberto surname: Chaparro Sánchez fullname: Chaparro Sánchez, Alberto – sequence: 7 givenname: Ericka surname: Pompa Mera fullname: Pompa Mera, Ericka – sequence: 8 givenname: Betzahida surname: Meneses Cisneros fullname: Meneses Cisneros, Betzahida – sequence: 9 givenname: Jesús Enrique surname: Gaytán Martínez fullname: Gaytán Martínez, Jesús Enrique |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/40478899$$D View this record in MEDLINE/PubMed |
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Keywords | metabolic syndrome integrase strand transfer inhibitors metabolic disturbances weight gain |
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Notes | Correspondence to Mara Soraya Rodríguez Evaristo, Internal Medicine Department, Hospital de Especialidades, "La Raza" National Medical Center, Seris y Vallejo S/N, Colonia La Raza, Postal code: 02990, Delegación Azcapotzalco, Mexico. Tel: +55 57245900 x23924; e-mail: marardguez_e@hotmail.comSupplemental digital content is available for this article. Direct URL citations appear in the printed text and are provided in the HTML and PDF versions of this article on the journal's Website (http://www.AIDSonline.com). |
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Snippet | Objective:Evidence suggests that patients initiating a second-generation integrase strand transfer inhibitors (INSTI)-based regimen may have a higher risk of... Evidence suggests that patients initiating a second-generation integrase strand transfer inhibitors (INSTI)-based regimen may have a higher risk of developing... |
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Title | Incidence of metabolic syndrome in people with HIV who start dolutegravir based-regimen compared with bictegravir based-regimen after 48 weeks |
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