“…ARHL is also characterized by impaired sound localization, reduced central auditory processing as well as reduced perception and understanding of speech in noisy environments [ 40 ]. The development of ARHL is suggested to be multifactorial, influenced by factors such as cochlear aging [ 38, 41 ], noise exposure [ 42, 43 ], gender [ 44 ], race [ 45, 46 ], genetic predisposition [ 47 ], environmental variables [ 48, 49 ], hypertension [ 50 ], and other health comorbidities, such as type 2 diabetes [ 51 ]. The main pathologies of ARHL are of cochlear origin, including loss of sensory (hair) cells, stria vascularis atrophy, auditory nerve degeneration, and loss of spiral ganglion neurons, and often coupled with changes in central auditory pathways [ 40, 52 ].…”