Insulin resistance in people living with HIV is associated with exposure to thymidine analogues and/or didanosine and prior immunodeficiency

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Background: As people living with HIV (PLWH) are growing older, there is increased incidence of metabolic diseases, including type 2 diabetes mellitus, for which insulin resistance is a key determinant. In this study, we aimed to investigate risk factors associated with insulin resistance in PLWH. Methods: We included well-treated PLWH without hepatitis co-infection, and with available fasting serum insulin and plasma glucose (n = 643) from the Copenhagen Comorbidity in HIV Infection Study. Insulin resistance was calculated using the homeostasis model assessment of insulin resistance (HOMA-IR). We investigated the association between risk factors and high HOMA-IR in a logistic regression model adjusted for age, sex, abdominal obesity, smoking status, and origin. When including use of thymidine analogues and/or didanosine in the model, we also adjusted for time with HIV. Results: Median (IQR) age of PLWH was 52 years (46–61), and 87% (n = 557) were male. Median (IQR) HOMA-IR was 1.86 (1.23–3.14) mmol/L × mU/L. Risk factors significantly associated with high HOMA-IR included older age, BMI ≥ 25, abdominal obesity, waist circumference, use of thymidine analogues and/or didanosine, time with HIV, and CD4+ nadir < 200 cells/µL. Conclusions: Insulin resistance in PLWH is associated with both use of thymidine analogues and/or didanosine and prior immunodeficiency suggesting that increased attention on blood glucose in these patients could be beneficial.

OriginalsprogEngelsk
Artikelnummer503
TidsskriftBMC Infectious Diseases
Vol/bind22
ISSN1471-2334
DOI
StatusUdgivet - 2022

Bibliografisk note

Funding Information:
J.H reports grant from Novo Nordisk Foundation and Righospitalet Research Council. M.H.S, M.G, A.M.R.J and J.G reports no conflicts of interest. T.B reports grants from Novo Nordisk Foundation, grants from Simonsen Foundation, grants and personal fees from GSK, grants and personal fees from Pfizer, personal fees from Boehringer Ingelheim, grants and personal fees from Gilead, personal fees from MSD, personal fees from Astra Zeneca, personal fees from Janssen, grants from Lundbeck Foundation, grants from Kai Hansen Foundation, personal fees from Pentabase ApS, grants from Erik and Susanna Olesen’s Charitable Fund, outside the submitted work. H.S reports Steno Collaborative Grant, Novo Nordisk Foundation and advisory board activity for Novo Nordisk. S.D.N. has received unrestricted research grants from Novo Nordisk Foundation, Lundbeck Foundation, Rigshospitalet Research Council. Travelling grants from Gilead. Advisory board activity for Gilead and MSD, all unrelated to this manuscript. All other authors report no conflicts of interest.

Funding Information:
The COCOMO 2-year follow-up was supported by an unrestricted research grant from Gilead Sciences, Inc, Novo Nordic Foundation and Rigshospitalet Research Council.

Publisher Copyright:
© 2022, The Author(s).

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