Drug-drug interactions when treating HIV-related metabolic disorders

被引:9
作者
Gutierrez, Maria del Mar [1 ]
Mateo, Ma Gracia [1 ]
Corbacho, Noemi [1 ]
Vidal, Francesc [2 ]
Domingo, Pere [1 ]
机构
[1] Hosp Santa Creu & Sant Pau, Inst Recerca, Dept Infect Dis, Barcelona, Spain
[2] Hosp Univ Joan XXIII, Inst Recerca Rovira & Virgili, HIV Infect Unit, Dept Internal Med, Tarragona, Spain
关键词
HIV infection; people living with HIV; combination antiretroviral therapy; drug-drug interactions; lipid-lowering agents; statins; fibrates; ezetimibe; biguanides; sulphonylureas; glitazones; glinides; DPP-4; inhibitors; Alpha-glucosidase inhibitors; allopurinol; weight-lowering agents; CLINICAL PHARMACOKINETICS; ANTIRETROVIRAL THERAPY; INDUCED RHABDOMYOLYSIS; REDUCTASE INHIBITORS; INSULIN SENSITIVITY; PROTEASE INHIBITORS; INTERACTION PROFILE; DIABETES-MELLITUS; SGLT2; INHIBITORS; GLYCEMIC CONTROL;
D O I
10.1080/17425255.2019.1667334
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Introduction: Drug-drug interactions (DDI) between antiretroviral drugs and drugs for the treatment of metabolic disturbances in people living with human immunodeficiency virus (HIV) (PLWH) have represented a problem of paramount importance in the recent times. The problem has been mainly driven by sharing common metabolizing pathways. This problem has classically been worsened by the frequent use of pharmacokinetic boosters to enhance protease inhibitors and some integrase inhibitors plasma levels. Areas covered: This article focuses on the interactions between antiretroviral drugs and those drugs used to treat metabolic disturbances which frequently appear in PLWH. These include dyslipidemia, diabetes mellitus, hyperuricemia, and finally, drugs for the treatment of overweight and clinical obesity. References from PubMed, Embase, or Web of Science, among others, were reviewed. Expert opinion: The advent of safer drugs, in terms of DDI, in the antiretroviral and the metabolic field,such as non-boosted antiretrovirals and drugs with divergent metabolizing paths. Besides, learning by the caregivers on how to decrease and manage DDI, together with the extensive use of online updated DDI databases, has undoubtedly minimized the problem. The foreseeable increase in the burden of HIV-associated comorbidities and their associated treatments anticipates further complexities in the management of DDI in PLWH.
引用
收藏
页码:787 / 802
页数:16
相关论文
共 135 条
  • [1] Effects of CYP3A4 inhibitors on the pharmacokinetics of maraviroc in healthy volunteers
    Abel, Samantha
    Russell, Deborah
    Taylor-Worth, Richard J.
    Ridgway, Caroline E.
    Muirhead, Gary J.
    [J]. BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2008, 65 : 27 - 37
  • [2] Simvastatin-induced rhabdomyolysis in an HIV-infected patient with coronary artery disease
    Aboulafia, DM
    Johnston, R
    [J]. AIDS PATIENT CARE AND STDS, 2000, 14 (01) : 13 - 18
  • [3] Association of serum lipid levels with HIV serostatus, specific antiretroviral agents, and treatment regimens
    Anastos, Kathryn
    Lu, Dalian
    Shi, Qiuhu
    Tien, Phyllis C.
    Kaplan, Robert C.
    Hessol, Nancy A.
    Cole, Steven
    Vigen, Cheryl
    Cohen, Mardge
    Young, Mary
    Justman, Jessica
    [J]. JAIDS-JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES, 2007, 45 (01) : 34 - 42
  • [4] [Anonymous], 2018, JUXT LOM
  • [5] [Anonymous], 2015, GENV ELV COB EMTR TE
  • [6] [Anonymous], 2018, TIV DOL
  • [7] [Anonymous], 2018, SIT JAN
  • [8] [Anonymous], 2016, JARD EMP, P19
  • [9] [Anonymous], IS RALT
  • [10] [Anonymous], 2009, REYAT AT