Evaluation of Drug Abuse by Hair Analysis and Self-Reported Use Among MSM Under PrEP: Results From a French Substudy of the ANRS-IPERGAY Trial.


Journal

Journal of acquired immune deficiency syndromes (1999)
ISSN: 1944-7884
Titre abrégé: J Acquir Immune Defic Syndr
Pays: United States
ID NLM: 100892005

Informations de publication

Date de publication:
15 04 2021
Historique:
received: 18 09 2020
accepted: 23 11 2020
pubmed: 5 1 2021
medline: 24 9 2021
entrez: 4 1 2021
Statut: ppublish

Résumé

We used the Agence nationale de Recherches sur le sida et les hépatites virales (ANRS)-IPERGAY trial to qualitatively and quantitatively measure drug use among men who have sex with men under preexposure prophylaxis using 2 different methods, to better understand and collectively respond to risky practices. We included 69 volunteers of the ANRS-IPERGAY trial. We measured drug use by 2 methods: (1) drug detection by hair analysis and (2) reported drug use by self-reported drug consumption. New psychoactive substances (NPS) and conventional drugs were detected in 53 of the 69 (77%) volunteers by hair analysis and in 39 of the 69 (57%) volunteers by questionnaires. On the 219 hair segments analyzed, the most commonly used drugs were cocaine in 47 of the 69 (68%), 3,4-methylenedioxymethamphetamine/ecstasy in 31 of the 69 (45%), and NPS in 27 of the 69 (39%). On the 1061 collected questionnaires, the most commonly used drugs were cocaine in 31 of the 69 (45%), 3,4-methylenedioxymethamphetamine/ecstasy in 29 of the 69 (42%), and NPS in 16 of the 69 (23%). Hair analysis detects more conventional drugs and/or NPS use (P < 0.05). Drug use identified by hair was significantly associated with a higher number of sexual partners in the past 2 months (P ≤ 0.001), more often casual partners (P ≤ 0.001), condomless anal sex (P ≤ 0.005), hardcore sexual practices (P ≤ 0.001), a higher number of sexually transmitted infections, and chemsex (P ≤ 0.05). Self-report drug use by questionnaires remains the reference tool for harm reduction at the individual level because of its feasibility and low cost. However, hair analysis is more sensitive, objectively assessing consumption, and interesting to understand uses and to be able to collectively respond to risky practices with adapted messages.

Sections du résumé

BACKGROUND
We used the Agence nationale de Recherches sur le sida et les hépatites virales (ANRS)-IPERGAY trial to qualitatively and quantitatively measure drug use among men who have sex with men under preexposure prophylaxis using 2 different methods, to better understand and collectively respond to risky practices.
METHOD
We included 69 volunteers of the ANRS-IPERGAY trial. We measured drug use by 2 methods: (1) drug detection by hair analysis and (2) reported drug use by self-reported drug consumption.
RESULTS
New psychoactive substances (NPS) and conventional drugs were detected in 53 of the 69 (77%) volunteers by hair analysis and in 39 of the 69 (57%) volunteers by questionnaires. On the 219 hair segments analyzed, the most commonly used drugs were cocaine in 47 of the 69 (68%), 3,4-methylenedioxymethamphetamine/ecstasy in 31 of the 69 (45%), and NPS in 27 of the 69 (39%). On the 1061 collected questionnaires, the most commonly used drugs were cocaine in 31 of the 69 (45%), 3,4-methylenedioxymethamphetamine/ecstasy in 29 of the 69 (42%), and NPS in 16 of the 69 (23%). Hair analysis detects more conventional drugs and/or NPS use (P < 0.05). Drug use identified by hair was significantly associated with a higher number of sexual partners in the past 2 months (P ≤ 0.001), more often casual partners (P ≤ 0.001), condomless anal sex (P ≤ 0.005), hardcore sexual practices (P ≤ 0.001), a higher number of sexually transmitted infections, and chemsex (P ≤ 0.05).
CONCLUSIONS
Self-report drug use by questionnaires remains the reference tool for harm reduction at the individual level because of its feasibility and low cost. However, hair analysis is more sensitive, objectively assessing consumption, and interesting to understand uses and to be able to collectively respond to risky practices with adapted messages.

Identifiants

pubmed: 33394814
doi: 10.1097/QAI.0000000000002610
pii: 00126334-202104150-00006
doi:

Substances chimiques

Anti-HIV Agents 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

552-561

Informations de copyright

Copyright © 2020 Wolters Kluwer Health, Inc. All rights reserved.

Déclaration de conflit d'intérêts

J.-M.M. reports receiving financial support as an adviser for Gilead Sciences, Merck, Janssen, Bristol-Myers Squibb, and ViiV Healthcare, and research grants from Gilead Sciences and Merck. F.R. reports receiving financial support as an adviser for Gilead Sciences, Merck, Janssen, and ViiV Healthcare, and research grants from Gilead Sciences. B.S. reports receiving support as an adviser for Gilead Sciences, Merck, Janssen, and Bristol-Myers Squibb, and research grants from ANRS, Fondation Pierre Bergé, Gilead Sciences, and Merck. L.C. has received research grants from ViiV Healthcare and Merck, personal fees from Mylan, and nonfinancial support from BMS, Gilead Science, Janssen Cilag, MSD, and ViiV Healthcare. G.P. has received consulting fees from Bristol-Myers Squibb, Boehringer Ingelheim, Tibotec, Nephrotek, Gilead, Roche, MSD, Abbott, and ViiV Healthcare, and research grants from Bristol-Myers Squibb and Gilead Sciences. E.C. reports receiving financial support as an adviser for Janssen, Merck, ViiV, and Novartis, and nonfinancial support from Gilead Sciences. J.C. reports receiving financial support as an adviser for Gilead Sciences, Bristol-Myers Squibb, and AbbVie. L.M. reports receiving grants from ANRS, the Bill & Melinda Gates Foundation, and Gilead. G. Peytavin has received travel grants, consultancy fees, honoraria, or study grants from various pharmaceutical companies, including Gilead Sciences, Janssen, Merck, and ViiV Healthcare. The other authors have no conflicts of interest to disclose.

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Auteurs

Julie Chas (J)

Département des Maladies Infectieuses, Hôpital Tenon, AP-HP, Paris, France.

Rebecca Bauer (R)

INSERM SC10 US19, Villejuif, France.

Islam Amine Larabi (IA)

Département de Pharmacologie-Toxicologie, Hôpital Raymond Poincaré, AP-HP, et MassSpecLab, Plateforme de Spectrométrie de Masse, Inserm U-1173, UFR des Sciences de la Santé Simone Veil, Université Paris-Saclay (Versailles Saint-Quentin-en-Yvelines), Garches, France.

Gilles Peytavin (G)

Département de Pharmacologie-Toxicologie, Hôpital Bichat Claude Bernard, AP-HP, et IAME, INSERM, UMRS1137, Université de Paris, Paris, France.

Perrine Roux (P)

Aix Marseille Université, INSERM, IRD, SESSTIM, Sciences Economiques & Sociales de la Santé & Traitement de l'Information Médicale, Marseille, France.
ORS PACA, Observatoire régional de la santé Provence-Alpes-Côte d'Azur, Marseille, France.

Eric Cua (E)

Département des Maladies Infectieuses, Hôpital de l'Archet, Nice, France.

Laurent Cotte (L)

Département des Maladies Infectieuses, Hôpital de la Croix Rousse, Hospices Civils de Lyon, Lyon, France.

Armelle Pasquet (A)

Département des Maladies Infectieuses, Hôpital G Dron, Centre Hospitalier Universitaire de Tourcoing, Tourcoing, France.

Catherine Capitant (C)

INSERM SC10 US19, Villejuif, France.

Laurence Meyer (L)

INSERM SC10 US19, Villejuif, France.
Université Paris Sud, Paris, France.

Francois Raffi (F)

Département des Maladies Infectieuses, Hôtel-Dieu, Nantes, France.

Bruno Spire (B)

Aix Marseille Université, INSERM, IRD, SESSTIM, Sciences Economiques & Sociales de la Santé & Traitement de l'Information Médicale, Marseille, France.
ORS PACA, Observatoire régional de la santé Provence-Alpes-Côte d'Azur, Marseille, France.

Gilles Pialoux (G)

Département des Maladies Infectieuses, Hôpital Tenon, AP-HP, Paris, France.
Sorbonne Université, Paris, France.

Jean-Michel Molina (JM)

Département de Maladies Infectieuses, Hôpital Lariboisière Saint-Louis, Paris, France.
Université de Paris, Paris, France; and.
INSERM U944, Paris, France.

Jean-Claude Alvarez (JC)

Département de Pharmacologie-Toxicologie, Hôpital Raymond Poincaré, AP-HP, et MassSpecLab, Plateforme de Spectrométrie de Masse, Inserm U-1173, UFR des Sciences de la Santé Simone Veil, Université Paris-Saclay (Versailles Saint-Quentin-en-Yvelines), Garches, France.

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