4.6 Article

Clinical Features and Potential Mechanisms Relating Neuropathological Biomarkers and Blood-Brain Barrier in Patients With Alzheimer's Disease and Hearing Loss

Journal

FRONTIERS IN AGING NEUROSCIENCE
Volume 14, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fnagi.2022.911028

Keywords

Alzheimer's disease; hearing loss; clinical features; neuropathological biomarkers of AD; blood-brain barrier; cerebrospinal fluid

Funding

  1. National Key Research and Development Program of China [2016YFC1306300, 2016YFC1306000]
  2. National Key R&D Program of China-European Commission Horizon 2020 [2017YFE0118800-779238]
  3. National Natural Science Foundation of China [81970992, 81571229, 81071015, 30770745]
  4. Capitals Funds for Health Improvement and Research (CFH) [2022-2-2048]
  5. Key Technology R&D Program of Beijing Municipal Education Commission [kz201610025030]
  6. Natural Science Foundation of Beijing, China [7082032]
  7. Key Project of Natural Science Foundation of Beijing, China [4161004]
  8. Project of Scientific and Technological Development of Traditional Chinese Medicine in Beijing [JJ2018-48]
  9. Capital Clinical Characteristic Application Research [Z121107001012161]
  10. High Level Technical Personnel Training Project of Beijing Health System, China [2009-3-26]
  11. Project of Beijing Institute for Brain Disorders [BIBD-PXM2013_014226_07_000084]
  12. Excellent Personnel Training Project of Beijing, China [20071D0300400076]
  13. Important National Science and Technology Specific Projects [2011ZX09102-003-01]
  14. National Key Technology Research and Development Program of the Ministry of Science and Technology of China [2013BAI09B03]
  15. Project of Construction of Innovative Teams and Teacher Career Development for Universities and Colleges Under Beijing Municipality [IDHT20140514]
  16. Beijing Healthcare Research Project, China [JING-15-2]
  17. Basic-Clinical Research Cooperation Funding of Capital Medical University, China [2015-JL-PT-X04, 10JL49, 14JL15]
  18. Natural Science Foundation of Capital Medical University, Beijing, China [PYZ2018077]
  19. Beijing Tiantan Hospital, Capital Medical University, China [2015-YQN-14, 2015-YQN-15, 2015-YQN-17]

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This study aimed to explore the clinical features and potential mechanisms of Alzheimer's disease (AD) and hearing loss (HL) by analyzing neuropathological biomarkers and blood-brain barrier (BBB). The results showed that AD patients with HL had significantly impaired overall cognitive function, memory, language, attention, execution, and activities of daily living (ADL). The potential mechanisms of AD-HL were elevated levels of AD neuropathological biomarker P-tau (S199) and BBB factor MMP-3, as well as correlations between P-tau (S199) and MMP-2/MMP-3 levels in cerebrospinal fluid (CSF).
BackgroundThe aim of this study was to explore clinical features and potential mechanisms relating neuropathological biomarkers and blood-brain barrier (BBB) in Alzheimer's disease (AD) and hearing loss (HL). Materials and MethodsA total of 65 patients with AD were recruited and auditory function was assessed by threshold of pure tone audiometry (PTA). Patients were divided into AD with HL (AD-HL) and AD with no HL (AD-nHL) groups based on the standard of World Health Organization. Clinical symptoms were assessed by multiple rating scales. The levels of neuropathological biomarkers of beta amyloid1-42 (A beta(1-42)) and multiple phosphorylated tau (P-tau), and BBB factors of matrix metalloproteinases (MMPs), receptor of advanced glycation end products, glial fibrillary acidic protein, and low-density lipoprotein receptor related protein 1 were measured. Results(1) Compared with AD-nHL group, AD-HL group had significantly impaired overall cognitive function and cognitive domains of memory, language, attention, execution, and activities of daily living (ADL) reflected by the scores of rating scales (P < 0.05). PTA threshold was significantly correlated with the impairments of overall cognitive function and cognitive domains of memory and language, and ADL in patients with AD (P < 0.05). (2) P-tau (S199) level was significantly increased in CSF from AD-HL group (P < 0.05), and was significantly and positively correlated with PTA threshold in patients with AD. (3) MMP-3 level was significantly elevated in CSF from AD-HL group (P < 0.05), and was significantly and positively correlated with PTA threshold in patients with AD (P < 0.05). (4) In AD-HL group, P-tau (S199) level was significantly and positively correlated with the levels of MMP-2 and MMP-3 in CSF (P < 0.05). ConclusionAD-HL patients have severely compromised overall cognitive function, multiple cognitive domains, and ADL. The potential mechanisms of AD-HL involve elevations of AD neuropathological biomarker of P-tau (S199) and BBB factor of MMP-3, and close correlations between P-tau (S199) and MMP-2/MMP-3 in CSF. Findings from this investigation highly suggest significance of early evaluation of HL for delaying AD progression, and indicate new directions of drug development by inhibiting neuropathological biomarkers of AD and protecting BBB.

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