Preclinical prospects of investigational agents for hearing loss treatment

被引:1
作者
Le Prell, Colleen G. [1 ,2 ,3 ]
机构
[1] Univ Texas Dallas, Dept Speech Language & Hearing, Richardson, TX USA
[2] Univ Texas Dallas, Callier Ctr Commun Disorders, Dallas, TX USA
[3] Callier Ctr Commun Disorders, 1966 Inwood Rd, Dallas, TX 75235 USA
关键词
Hearing loss; hearing loss prevention; noise-induced hearing loss; drug-induced hearing loss; sensorineural hearing loss; gene therapy; TASK-FORCE GUIDELINES; CISPLATIN-INDUCED OTOTOXICITY; SODIUM THIOSULFATE; NOISE EXPOSURE; COCHLEAR IMPLANTATION; DEPENDENT PROTECTION; DEMENTIA PREVENTION; CLINICAL-ASSESSMENT; ANIMAL-MODELS; INNER-EAR;
D O I
10.1080/13543784.2023.2253141
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: : Hearing loss has a high prevalence, with aging, noise exposure, ototoxic drug therapies, and genetic mutations being some of the leading causes of hearing loss. Health conditions such as cardiovascular disease and diabetes are associated with hearing loss, perhaps due to shared vascular pathology in the ear and in other tissues.Areas Covered: : Issues in the design of preclinical research preclude the ability to make comparisons regarding the relative efficacy of different drugs of interest for possible hearing loss prevention or hearing restoration. This has not slowed the advancement of candidate therapeutics into human clinical testing. There is a robust pipeline with drugs that have different mechanisms of action providing diverse candidate therapies and opportunities for combination therapies to be considered.Expert Opinion: : Much of the preclinical research literature lacks standard study design elements such as dose response testing, and lack of standardization of test protocols significantly limits conclusions regarding relative efficacy. Nonetheless, the many positive results to date have supported translation of preclinical efforts into clinical trials assessing potential human benefits. Approval of the first hearing loss prevention therapeutic is a major success, providing a pathway for other drugs to follow.
引用
收藏
页码:685 / 692
页数:8
相关论文
共 88 条
[1]  
Abi-Hachem Ralph N, 2010, Recent Pat CNS Drug Discov, V5, P147
[2]   Prevalence of hearing loss and differences by demographic characteristics among US adults - Data from the National Health and Nutrition Examination Survey, 1999-2004 [J].
Agrawal, Yuri ;
Platz, Elizabeth A. ;
Niparko, John K. .
ARCHIVES OF INTERNAL MEDICINE, 2008, 168 (14) :1522-1530
[3]   Emerging therapies for human hearing loss [J].
Ajay, Elise ;
Gunewardene, Niliksha ;
Richardson, Rachael .
EXPERT OPINION ON BIOLOGICAL THERAPY, 2022, 22 (06) :689-705
[4]   Do we need audiogram-based prescriptions? A systematic review [J].
Almufarrij, Ibrahim ;
Dillon, Harvey ;
Munro, Kevin J. .
INTERNATIONAL JOURNAL OF AUDIOLOGY, 2023, 62 (06) :500-511
[5]   Pharmaceutical otoprotection strategies to prevent impulse noise-induced hearing loss [J].
Bielefeld, Eric C. ;
Harrison, Ryan T. ;
DeBacker, J. Riley .
JOURNAL OF THE ACOUSTICAL SOCIETY OF AMERICA, 2019, 146 (05) :3790-3799
[6]   Advances and Challenges in Pharmaceutical Therapies to Prevent and Repair Cochlear Injuries From Noise [J].
Bielefeld, Eric C. ;
Kobel, Megan J. .
FRONTIERS IN CELLULAR NEUROSCIENCE, 2019, 13
[7]   Differences in Ototoxicity across Species [J].
Blakley, Brian W. ;
Hochman, Jordan ;
Wellman, Mark ;
Gooi, Adrian ;
Hussain, Abdulmohsen E. .
JOURNAL OF OTOLARYNGOLOGY-HEAD & NECK SURGERY, 2008, 37 (05) :700-703
[8]   Use of the auditory brainstem response for assessment of cochlear synaptopathy in humans [J].
Bramhall, Naomi F. .
JOURNAL OF THE ACOUSTICAL SOCIETY OF AMERICA, 2021, 150 (06) :4440-4451
[9]   Cisplatin is retained in the cochlea indefinitely following chemotherapy [J].
Breglio, Andrew M. ;
Rusheen, Aaron E. ;
Shide, Eric D. ;
Fernandez, Katharine A. ;
Spielbauer, Katie K. ;
McLachlin, Katherine M. ;
Hall, Matthew D. ;
Amable, Lauren ;
Cunningham, Lisa L. .
NATURE COMMUNICATIONS, 2017, 8
[10]   Sodium Thiosulfate for Protection from Cisplatin-Induced Hearing Loss [J].
Brock, P. R. ;
Maibach, R. ;
Childs, M. ;
Rajput, K. ;
Roebuck, D. ;
Sullivan, M. J. ;
Laithier, V. ;
Ronghe, M. ;
Dall'Igna, P. ;
Hiyama, E. ;
Brichard, B. ;
Skeen, J. ;
Mateos, M. E. ;
Capra, M. ;
Rangaswami, A. A. ;
Ansari, M. ;
Rechnitzer, C. ;
Veal, G. J. ;
Covezzoli, A. ;
Brugieres, L. ;
Perilongo, G. ;
Czauderna, P. ;
Morland, B. ;
Neuwelt, E. A. .
NEW ENGLAND JOURNAL OF MEDICINE, 2018, 378 (25) :2376-2385