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Endogenous α1‐antitrypsin levels in the perilymphatic fluid correlates with severity of hearing loss
Author(s) -
ElSaied Sabri,
Schmitt Heike,
Durisin Martin,
Joshua BenZion,
Abu Tailakh Muhammad,
Prenzler Nils,
Lenarz Thomas,
Kaplan Daniel M.,
Lewis Eli C.,
Warnecke Athanasia
Publication year - 2020
Publication title -
clinical otolaryngology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.914
H-Index - 68
eISSN - 1749-4486
pISSN - 1749-4478
DOI - 10.1111/coa.13541
Subject(s) - medicine , perilymph , hearing loss , cochlear implantation , audiology , cochlea
Objectives To determine the levels of endogenous α1‐antitrypsin in the perilymph of patients undergoing cochlear implant (CI), and its reverse association with the severity of hearing loss. Study Design Retrospective study. Setting Tertiary care university hospital. Participants The study includes 38 patients undergoing CI surgery, 11 patients diagnosed with congenital deafness and 27 non‐congenital deafness, eight patients diagnosed with moderate hearing loss (N = 8; PTA = 70 dB), severe hearing loss (N = 11; PTA 70‐90 dB) and profound hearing loss (N = 19; PTA > 90 dB). Main outcome and measure 1 to 12 μL perilymphatic fluids were collected by micropipette. α1‐antitrypsin levels were determined, and current and historic audiological parameters were obtained. Results The congenital and non‐congenital group exhibited AAT concentrations of 2.5 ± 1.9 × 10 6 LFQ and 3.2 ± 1.2 × 10 6 LFQ, respectively (mean ± SD; P = .38). Mean levels of α1‐antitrypsin in the perilymph fluid within the moderate group was 3.64 × 10 6 ± 2.1 × 10 6 LFQ vs 3.5 × 10 6 ± 1.2 × 10 6 in severe hearing loss ( P = .81) and 2.4 × 10 6 ± 1.1 × 10 6 LFQ in the profound hearings loss group ( P = .06). The difference in levels of AAT in samples from the severe hearings loss group vs the profound hearings loss group reached statistical significance ( P = .04). Conclusion Insufficiency in α1‐antitrypsin levels in the perilymph fluid of the inner ear appears to display a relationship with the severity of hearing loss. The prospect of introducing clinical‐grade plasma‐purified α1‐antitrypsin directly onto the site of cochlear injury deserves thorough investigation.