Abstract

Persons living with HIV (PLWH) may have increased incidence of cardiovascular events and longer QTc intervals than uninfected persons. We aimed to investigate the incidence and risk factors of de novo major electrocardiogram (ECG) abnormalities and QTc prolongation in well-treated PLWH. We included virologically suppressed PLWH without major ECG abnormalities, who attended the 2-year follow-up in the Copenhagen comorbidity in HIV infection (COCOMO) study. ECGs were categorized according to Minnesota Code Manual. We defined de novo major ECG abnormalities as new major Minnesota Code Manual abnormalities. Prolonged QTc was defined as QTc > 460 ms in females and QTc > 450 ms in males. Of 667 PLWH without major ECG abnormalities at baseline, 34 (5%) developed de novo major ECG abnormalities after a median of 2.3 years. After adjustment, age (RR: 1.57 [1.08–2.28] per decade older), being underweight (RR: 5.79 [1.70–19.71]), current smoking (RR: 2.34 [1.06–5.16]), diabetes (RR: 3.89 [1.72–8.80]) and protease inhibitor use (RR: 2.45 [1.27–4.74) were associated with higher risk of getting de novo major ECG abnormalities. Of PLWH without prolonged QTc at baseline, only 11 (1.6%) participants developed de novo prolonged QTc. Five percent of well-treated PLWH acquired de novo major ECG abnormalities and protease inhibitor use was associated with more than twice the risk of de novo major ECG abnormalities. De novo prolonged QTc was rare and did not seem to constitute a problem in well-treated PLWH.

Highlights

  • Persons living with HIV (PLWH) may have increased incidence of cardiovascular events and longer QTc intervals than uninfected persons

  • Persons living with HIV (PLWH) have increased risk of cardiovascular disease (CVD), and the rate of sudden cardiac death in PLWH may be as high as 4.5 times of that expected in the uninfected p­ opulation[1,2]

  • No specific antiretroviral drug class was associated with de novo major ECG abnormalities and CD4 count was not associated with de novo major ECG abnormalities.In a sensitivity analysis, we examined whether further adjustment for serum Low density lipoprotein (LDL) concentration would attenuate the association between protease inhibitor use and de novo major ECG abnormality at follow-up

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Summary

Introduction

Persons living with HIV (PLWH) may have increased incidence of cardiovascular events and longer QTc intervals than uninfected persons. We aimed to investigate the incidence and risk factors of de novo major electrocardiogram (ECG) abnormalities and QTc prolongation in well-treated PLWH. We recently reported higher odds of pathological Q-waves and prolonged corrected QT interval (QTc), markers of coronary artery disease and sudden cardiac death, respectively, among PLWH than among uninfected c­ ontrols[5], but little is known about incidence of ECG abnormalities in PLWH. HIV-related risk factors including chronic inflammation and use of protease inhibitors as well as specific nonnucleoside reverse transcriptase inhibitors, such as efavirenz and rilpivirine, have been associated with ischemic heart disease and QTc prolongation, r­ espectively[6,7,8,9,10,11]. We hypothesised that both traditional and HIV-related variables, efavirenz, rilpivirine

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