Early versus deferred antiretroviral therapy initiation and long-term cardiovascular disease outcomes in people with HIV: The START study - Scorecard - MDSpire

Early versus deferred antiretroviral therapy initiation and long-term cardiovascular disease outcomes in people with HIV: The START study

  • By

  • Nila J Dharan

  • Shweta Sharma

  • Alejandro Arenas-Pinto

  • Daniel Duprez

  • Vicente Estrada

  • Karen Ha

  • Mariana Angelica Kundro

  • Rosie Mngqibisa

  • Henry Mugerwa

  • David Munroe

  • Rakan Nasreddine

  • Tess E Peterson

  • Irini Sereti

  • Janine M Trevillyan

  • Jason V Baker

  • Gail V Matthews

  • Andrew N Phillips

  • for the INSIGHT START Study Group

  • September 15, 2025

  • 0 min

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Clinical Scorecard: Comparison of Immediate and Delayed Antiretroviral Therapy on Long-Term Cardiovascular Outcomes in HIV-Infected Individuals: Findings from the START Trial

At a Glance

CategoryDetail
ConditionCardiovascular disease (CVD) in people with HIV (PHIV)
Key MechanismsHIV viremia, chronic inflammation, immune activation, traditional cardiometabolic risk factors, and ART-related toxicities
Target PopulationART-naïve adult people with HIV with CD4+ counts > 500 cells/µL
Care SettingHIV clinical care and research settings with long-term follow-up

Key Highlights

  • No difference in long-term CVD event rates between immediate and deferred ART initiation over median 9.3 years follow-up.
  • Possible cardiovascular benefit of immediate ART initiation observed in female participants but not males.
  • Traditional CVD risk factors and HIV-specific factors both contribute to increased CVD risk in PHIV.

Guideline-Based Recommendations

Diagnosis

  • Assess traditional CVD risk factors (hypertension, dyslipidemia, diabetes, smoking) in PHIV.
  • Monitor HIV-specific factors including viral load, immune activation, and inflammation markers.

Management

  • Initiate ART promptly to reduce HIV viremia and related inflammation.
  • Consider cardiovascular risk when selecting antiretroviral agents due to potential toxicities.
  • Manage traditional CVD risk factors aggressively in PHIV.

Monitoring & Follow-up

  • Regular follow-up of CD4+ count, viral load, and fasting lipids.
  • Monitor for development of CVD events including myocardial infarction, stroke, and coronary revascularization.
  • Long-term surveillance for ART-related metabolic side effects.

Risks

  • Delayed ART initiation does not reduce CVD events and may miss potential benefits, especially in females.
  • Certain antiretrovirals may increase risk of MI, dyslipidemia, insulin resistance, and weight gain.

Patient & Prescribing Data

ART-naïve adults with HIV and high CD4+ counts (>500 cells/µL)

Immediate ART initiation reduces overall morbidity and mortality but does not significantly reduce CVD events compared to deferred ART; potential sex-specific cardiovascular benefits warrant further study.

Clinical Best Practices

  • Evaluate and manage traditional and HIV-specific cardiovascular risk factors in all PHIV.
  • Start ART promptly regardless of CD4+ count to improve overall outcomes.
  • Tailor ART regimens considering individual cardiovascular risk profiles.
  • Maintain long-term follow-up for CVD event surveillance and metabolic monitoring.
  • Recognize potential sex differences in cardiovascular outcomes related to ART timing.

References

Original Source(s)

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