The influence of age-associated comorbidities on responses to combination antiretroviral therapy in older people living with HIV.


Journal

Journal of the International AIDS Society
ISSN: 1758-2652
Titre abrégé: J Int AIDS Soc
Pays: Switzerland
ID NLM: 101478566

Informations de publication

Date de publication:
02 2019
Historique:
received: 18 06 2018
accepted: 19 12 2018
entrez: 26 2 2019
pubmed: 26 2 2019
medline: 6 2 2020
Statut: ppublish

Résumé

Multiple comorbidities among HIV-positive individuals may increase the potential for polypharmacy causing drug-to-drug interactions and older individuals with comorbidities, particularly those with cognitive impairment, may have difficulty in adhering to complex medications. However, the effects of age-associated comorbidities on the treatment outcomes of combination antiretroviral therapy (cART) are not well known. In this study, we investigated the effects of age-associated comorbidities on therapeutic outcomes of cART in HIV-positive adults in Asian countries. Patients enrolled in the TREAT Asia HIV Observational Database cohort and on cART for more than six months were analysed. Comorbidities included hypertension, diabetes, dyslipidaemia and impaired renal function. Treatment outcomes of patients ≥50 years of age with comorbidities were compared with those <50 years and those ≥50 years without comorbidities. We analysed 5411 patients with virological failure and 5621 with immunologic failure. Our failure outcomes were defined to be in-line with the World Health Organization 2016 guidelines. Cox regression analysis was used to analyse time to first virological and immunological failure. The incidence of virologic failure was 7.72/100 person-years. Virological failure was less likely in patients with better adherence and higher CD4 count at cART initiation. Those acquiring HIV through intravenous drug use were more likely to have virological failure compared to those infected through heterosexual contact. On univariate analysis, patients aged <50 years without comorbidities were more likely to experience virological failure than those aged ≥50 years with comorbidities (hazard ratio 1.75, 95% confidence interval (CI) 1.31 to 2.33, p < 0.001). However, the multivariate model showed that age-related comorbidities were not significant factors for virological failure (hazard ratio 1.31, 95% CI 0.98 to 1.74, p = 0.07). There were 391 immunological failures, with an incidence of 2.75/100 person-years. On multivariate analysis, those aged <50 years without comorbidities (p = 0.025) and age <50 years with comorbidities (p = 0.001) were less likely to develop immunological failure compared to those aged ≥50 years with comorbidities. In our Asia regional cohort, age-associated comorbidities did not affect virologic outcomes of cART. Among those with comorbidities, patients <50 years old showed a better CD4 response.

Identifiants

pubmed: 30803162
doi: 10.1002/jia2.25228
pmc: PMC6389354
doi:

Substances chimiques

Anti-HIV Agents 0
Anti-Retroviral Agents 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e25228

Subventions

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

Informations de copyright

© 2019 The Authors. Journal of the International AIDS Society published by John Wiley & Sons Ltd on behalf of the International AIDS Society.

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Auteurs

Mi Young Ahn (MY)

Department of Internal Medicine, Yonsei University College of Medicine, Seoul, South Korea.
AIDS Research Institute, Yonsei University College of Medicine, Seoul, South Korea.
Department of Internal Medicine, Seoul Medical Center, Seoul, South Korea.

Awachana Jiamsakul (A)

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

Suwimon Khusuwan (S)

Chiangrai Prachanukroh Hospital, Chiang Rai, Thailand.

Vohith Khol (V)

National Center for HIV/AIDS, Dermatology & STDs, Phnom Penh, Cambodia.

Thuy T Pham (TT)

Bach Mai Hospital, Hanoi, Vietnam.

Romanee Chaiwarith (R)

Research Institute for Health Sciences, Chiang Mai, Thailand.

Anchalee Avihingsanon (A)

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

Nagalingeswaran Kumarasamy (N)

Chennai Antiviral Research and Treatment Clinical Research Site (CART CRS), YRGCARE Medical Centre, VHS, Chennai, India.

Wing Wei Wong (WW)

Taipei Veterans General Hospital, Taipei, Taiwan.

Sasisopin Kiertiburanakul (S)

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

Sanjay Pujari (S)

Institute of Infectious Diseases, Pune, India.

Kinh V Nguyen (KV)

National Hospital for Tropical Diseases, Hanoi, Vietnam.

Man Po Lee (MP)

Queen Elizabeth Hospital, Hong Kong SAR, China.

Adeeba Kamarulzaman (A)

University Malaya Medical Centre, Kuala Lumpur, Malaysia.

Fujie Zhang (F)

Beijing Ditan Hospital, Capital Medical University, Beijing, China.

Rossana Ditangco (R)

Research Institute for Tropical Medicine, Muntinlupa City, Philippines.

Tuti P Merati (TP)

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

Evy Yunihastuti (E)

Faculty of Medicine Universitas Indonesia - Dr. Cipto Mangunkusumo General Hospital, Jakarta, Indonesia.

Oon Tek Ng (OT)

Tan Tock Seng Hospital, Singapore City, Singapore.

Benedict L H Sim (BLH)

Hospital Sungai Buloh, Sungai Buloh, Malaysia.

Junko Tanuma (J)

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

Winai Ratanasuwan (W)

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

Jeremy Ross (J)

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

Jun Yong Choi (JY)

Department of Internal Medicine, Yonsei University College of Medicine, Seoul, South Korea.
AIDS Research Institute, Yonsei University College of Medicine, Seoul, South Korea.

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Classifications MeSH