Fenofibrate and Telmisartan in the Management of Abdominal Aortic Aneurysm

被引:10
作者
Rowbotham, Sophie E. [1 ,2 ]
Krishna, Smriti M. [3 ]
Moran, Corey S. [3 ]
Golledge, Jonathan [3 ]
机构
[1] Univ Queensland, Sch Med, Herston, Qld 4006, Australia
[2] Royal Brisbane & Womens Hosp, Dept Vasc Surg, Herston, Qld 4029, Australia
[3] James Cook Univ, Queensland Res Ctr Peripheral Vasc Dis, Coll Med & Dent, Townsville, Qld 4811, Australia
关键词
Abdominal aortic aneurysm; telmisartan; fenofibrate; osteopontin; angiotensin; clinical trial; E-DEFICIENT MICE; RANDOMIZED CONTROLLED-TRIAL; ACTIVATED-RECEPTOR-GAMMA; ANGIOTENSIN-II FORMATION; SMOOTH-MUSCLE-CELLS; MOUSE MODEL; PPAR-ALPHA; VASCULAR-DISEASE; CLINICAL-TRIAL; OSTEOPONTIN;
D O I
10.2174/1389450119666171227224655
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Objective: This mini-review provides the rationale and updated progress for ongoing randomized controlled trials assessing fenofibrate and telmisartan efficacy to limit abdominal aortic aneurysm (AAA) growth. Methods/Results: There remains an urgent need to identify a drug therapy that will limit AAA growth. Data from preclinical and human studies indicate that fenofibrate and telmisartan have the potential to slow aortic destruction. Fenofibrate has been shown to reduce serum and tissue levels of the pro-inflammatory protein osteopontin, as well as reducing macrophage recruitment to the aortic wall, both of which are integral processes in the development and progression of AAAs. Telmisartan acts via blockade of the angiotensin II receptor, type 1, and also as a peroxisome proliferator-activated receptor gamma agonist. In turn, this inhibits the production of a range of biomarkers associated with AAA progression, including transforming growth factor-beta one, osteoprotegerin, osteopontin and matrix metalloproteinase-9. Based on these findings, there are currently three randomized controlled trials assessing both fenofibrate and telmisartan as potential interventions to limit aneurysm growth in AAA patients. Conclusion: Fenofibrate and telmisartan have potential as repurposed medications to limit AAA growth, and randomized trials for further assessment in AAA patients are ongoing.
引用
收藏
页码:1241 / 1246
页数:6
相关论文
共 79 条
  • [21] Obesity, adipokines, and abdominal aortic aneurysm - Health in men study
    Golledge, Jonathan
    Clancy, Paula
    Jamrozik, Konrad
    Norman, Paul E.
    [J]. CIRCULATION, 2007, 116 (20) : 2275 - 2279
  • [22] Association between osteopontin and human abdominal aortic aneurysm
    Golledge, Jonathan
    Muller, Juanita
    Shephard, Neil
    Clancy, Paula
    Smallwood, Linda
    Moran, Corey
    Dear, Anthony E.
    Palmer, Lyle J.
    Norman, Paul E.
    [J]. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2007, 27 (03) : 655 - 660
  • [23] Abdominal aortic aneurysm - Pathogenesis and implications for management
    Golledge, Jonathan
    Muller, Juanita
    Daugherty, Alan
    Norman, Paul
    [J]. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2006, 26 (12) : 2605 - 2613
  • [24] Challenges and opportunities in limiting abdominal aortic aneurysm growth
    Golledge, Jonathan
    Norman, Paul E.
    Murphy, Michael P.
    Dalman, Ronald L.
    [J]. JOURNAL OF VASCULAR SURGERY, 2017, 65 (01) : 225 - 233
  • [25] Association Between Serum Lipoproteins and Abdominal Aortic Aneurysm
    Golledge, Jonathan
    Van Bockxmeer, Frank
    Jamrozik, Konrad
    McCann, Moira
    Norman, Paul E.
    [J]. AMERICAN JOURNAL OF CARDIOLOGY, 2010, 105 (10) : 1480 - 1484
  • [26] Peroxisome proliferator-activated receptor ligands reduce aortic dilatation in a mouse model of aortic aneurysm
    Golledge, Jonathan
    Cullen, Bradford
    Rush, Catherine
    Moran, Corey S.
    Secomb, Emma
    Wood, Frances
    Daugherty, Alan
    Campbell, Julie H.
    Norman, Paul E.
    [J]. ATHEROSCLEROSIS, 2010, 210 (01) : 51 - 56
  • [27] Circulating Markers of Abdominal Aortic Aneurysm Presence and Progression
    Golledge, Jonathan
    Tsao, Philip S.
    Dalman, Ronald L.
    Norman, Paul E.
    [J]. CIRCULATION, 2008, 118 (23) : 2382 - 2392
  • [28] Fenofibrate reduces plasma cholesteryl ester transfer from HDL to VLDL and normalizes the atherogenic, dense LDL profile in combined hyperlipidemia
    Guerin, M
    Bruckert, E
    Dolphin, PJ
    Turpin, G
    Chapman, MJ
    [J]. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1996, 16 (06) : 763 - 772
  • [29] Losartan, an AT1 antagonist, prevents aortic aneurysm in a mouse model of Marfan syndrome
    Habashi, JP
    Judge, DP
    Holm, TM
    Cohn, RD
    Loeys, BL
    Cooper, TK
    Myers, L
    Klein, EC
    Liu, GS
    Calvi, C
    Podowski, M
    Neptune, ER
    Halushka, MK
    Bedja, D
    Gabrielson, K
    Rifkin, DB
    Carta, L
    Ramirez, F
    Huso, DL
    Dietz, HC
    [J]. SCIENCE, 2006, 312 (5770) : 117 - 121
  • [30] Attenuation of cardiac dysfunction by a PPAR-α agonist is associated with down-regulation of redox-regulated transcription factors
    Ichihara, Sahoko
    Obata, Koji
    Yamada, Yoshiji
    Nagata, Kohzo
    Noda, Akiko
    Ichihara, Gaku
    Yamada, Akira
    Kato, Tomoko
    Izawa, Hideo
    Murohara, Toyoaki
    Yokota, Mitsuhiro
    [J]. JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2006, 41 (02) : 318 - 329