Cardiovascular disease incidence projections in the TREAT Asia HIV Observational Database (TAHOD).


Journal

Antiviral therapy
ISSN: 2040-2058
Titre abrégé: Antivir Ther
Pays: England
ID NLM: 9815705

Informations de publication

Date de publication:
2019
Historique:
accepted: 11 02 2019
pubmed: 6 3 2019
medline: 1 7 2020
entrez: 6 3 2019
Statut: ppublish

Résumé

We aimed to project the 10-year future incidence of cardiovascular disease (CVD) and model several intervention scenarios based on a multi-site Asian HIV-positive cohort. Analyses were based on patients recruited to the TREAT Asia HIV Observational Database (TAHOD), consisting of 21 sites in 12 countries. Patients on triple antiretroviral therapy (ART) were included if they were alive, without previous CVD, and had data on CVD risk factors. Annual new CVD events for 2019-2028 were estimated with the D:A:D equation, accounting for age- and sex-adjusted mortality. Modelled intervention scenarios were treatment of high total cholesterol, low high-density lipoprotein cholesterol (HDL) or high blood pressure, abacavir or lopinavir substitution, and smoking cessation. Of 3,703 included patients, 69% were male, median age was 46 (IQR 40-53) years and median time since ART initiation was 9.8 years (IQR 7.5-14.1). Cohort incidence rates of CVD were projected to increase from 730 per 100,000 person-years (pys) in 2019 to 1,432 per 100,000 pys in 2028. In the modelled intervention scenarios, most events can be avoided by smoking cessation, abacavir substitution, lopinavir substitution, decreasing total cholesterol, treating high blood pressure and increasing HDL. Our projections suggest a doubling of CVD incidence rates in Asian HIV-positive adults in our cohort. An increase in CVD can be expected in any ageing population, however, according to our models, this can be close to averted by interventions. Thus, there is an urgent need for risk screening and integration of HIV and CVD programmes to reduce the future CVD burden.

Sections du résumé

BACKGROUND
We aimed to project the 10-year future incidence of cardiovascular disease (CVD) and model several intervention scenarios based on a multi-site Asian HIV-positive cohort.
METHODS
Analyses were based on patients recruited to the TREAT Asia HIV Observational Database (TAHOD), consisting of 21 sites in 12 countries. Patients on triple antiretroviral therapy (ART) were included if they were alive, without previous CVD, and had data on CVD risk factors. Annual new CVD events for 2019-2028 were estimated with the D:A:D equation, accounting for age- and sex-adjusted mortality. Modelled intervention scenarios were treatment of high total cholesterol, low high-density lipoprotein cholesterol (HDL) or high blood pressure, abacavir or lopinavir substitution, and smoking cessation.
RESULTS
Of 3,703 included patients, 69% were male, median age was 46 (IQR 40-53) years and median time since ART initiation was 9.8 years (IQR 7.5-14.1). Cohort incidence rates of CVD were projected to increase from 730 per 100,000 person-years (pys) in 2019 to 1,432 per 100,000 pys in 2028. In the modelled intervention scenarios, most events can be avoided by smoking cessation, abacavir substitution, lopinavir substitution, decreasing total cholesterol, treating high blood pressure and increasing HDL.
CONCLUSIONS
Our projections suggest a doubling of CVD incidence rates in Asian HIV-positive adults in our cohort. An increase in CVD can be expected in any ageing population, however, according to our models, this can be close to averted by interventions. Thus, there is an urgent need for risk screening and integration of HIV and CVD programmes to reduce the future CVD burden.

Identifiants

pubmed: 30833516
doi: 10.3851/IMP3298
pmc: PMC6728217
mid: NIHMS1019415
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

271-279

Subventions

Organisme : NIAID NIH HHS
ID : U01 AI069907
Pays : United States

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Auteurs

Rimke Bijker (R)

The Kirby Institute, UNSW Sydney, Sydney, NSW, Australia.

Nagalingeswaran Kumarasamy (N)

YRGCARE Medical Centre, Chennai, India.

Sasisopin Kiertiburanakul (S)

Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.

Sanjay Pujari (S)

Institute of Infectious Diseases, Pune, India.

Wilson Lam (W)

Queen Elizabeth Hospital, Kowloon, Hong Kong.

Romanee Chaiwarith (R)

Research Institute for Health Sciences, Chiang Mai University, Chiang Mai, Thailand.

Wing W Wong (WW)

Taipei Veterans General Hospital, Taipei, Taiwan.

Adeeba Kamarulzaman (A)

University Malaya Medical Centre, Kuala Lumpur, Malaysia.

Pacharee Kantipong (P)

Chiangrai Prachanukroh Hospital, Chiang Rai, Thailand.

Anchalee Avihingsanon (A)

HIV-NAT/The Thai Red Cross AIDS Research Centre, Bangkok, Thailand.

Kinh V Nguyen (KV)

National Hospital for Tropical Diseases, Hanoi, Vietnam.

Junko Tanuma (J)

National Center for Global Health and Medicine, Tokyo, Japan.

Oon Tek Ng (OT)

Department of Infectious Diseases, Tan Tock Seng Hospital, Singapore.

Benedict Lh Sim (BL)

Hospital Sungai Buloh, Sungai Buloh, Malaysia.

Tuti P Merati (TP)

Faculty of Medicine Udayana University & Sanglah Hospital, Bali, Indonesia.

Jun Y Choi (JY)

Division of Infectious Diseases, Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Republic of Korea.

Rossana Ditangco (R)

Research Institute for Tropical Medicine, Manila, Philippines.

Evy Yunihastuti (E)

Working Group on AIDS, Faculty of Medicine, University of Indonesia/Cipto Mangunkusumo Hospital, Jakarta, Indonesia.

Ly P Sun (LP)

National Center for HIV/AIDS, Dermatology & STDs, and University of Health Sciences, Phnom Penh, Cambodia.

Cuong D Do (CD)

Bach Mai Hospital, Hanoi, Vietnam.

Jeremy Ross (J)

TREAT Asia, amfAR - The Foundation for AIDS Research, Bangkok, Thailand.

Matthew Law (M)

The Kirby Institute, UNSW Sydney, Sydney, NSW, Australia.

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