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Tear neuropeptide Y as a non-invasive marker of peripheral microvascular complications in type 1 diabetes.
Britten-Jones, Alexis Ceecee; Wu, Mengliang; Roberts, Leslie J; MacIsaac, Richard J; Jiao, Haihan; Craig, Jennifer P; Chinnery, Holly R; Downie, Laura E.
Affiliation
  • Britten-Jones AC; Department of Optometry and Vision Sciences, The University of Melbourne, Parkville, VIC, Australia.
  • Wu M; Department of Optometry and Vision Sciences, The University of Melbourne, Parkville, VIC, Australia.
  • Roberts LJ; Department of Medicine, St Vincent's Hospital Melbourne, University of Melbourne, Fitzroy, VIC, Australia; Centre for Clinical Neurosciences and Neurological Research, St Vincent's Hospital Melbourne, Fitzroy, Australia.
  • MacIsaac RJ; Department of Medicine, St Vincent's Hospital Melbourne, University of Melbourne, Fitzroy, VIC, Australia; Department of Diabetes & Endocrinology, St Vincent's Hospital Melbourne, Fitzroy, VIC, Australia; Australian Centre for Accelerating Diabetes Innovations (ACADI), University of Melbourne, P
  • Jiao H; Department of Optometry and Vision Sciences, The University of Melbourne, Parkville, VIC, Australia; Department of Anatomy and Physiology, The University of Melbourne, Parkville, VIC, Australia.
  • Craig JP; Department of Ophthalmology, Aotearoa New Zealand National Eye Centre, The University of Auckland, Auckland, New Zealand.
  • Chinnery HR; Department of Optometry and Vision Sciences, The University of Melbourne, Parkville, VIC, Australia.
  • Downie LE; Department of Optometry and Vision Sciences, The University of Melbourne, Parkville, VIC, Australia. Electronic address: ldownie@unimelb.edu.au.
Ocul Surf ; 34: 309-316, 2024 Aug 15.
Article in En | MEDLINE | ID: mdl-39153598
ABSTRACT

AIMS:

To investigate tear neuropeptide Y (NPY) and substance P concentrations in individuals with type 1 diabetes, comparing those with and without both diabetic retinopathy (DR) and peripheral neuropathy.

METHODS:

This cross-sectional study involved 41 participants with type 1 diabetes and none to moderate DR, and 22 healthy controls. Assessments included clinical ocular surface parameters, quantification of corneal nerve attributes (based on in vivo confocal microscopy imaging), DR grading, and evaluation for small and large fibre neuropathy. Concentrations of NPY and substance P in tear samples were measured using enzyme-linked immunosorbent assay.

RESULTS:

Mean (± standard deviation) tear NPY concentrations in participants with type 1 diabetes and length-dependent small fibre neuropathy (SFN) was lower than in controls (10.84 ± 4.10 ng/mL vs 14.72 ± 3.12 ng/mL; p=0.004), but not significantly different from type 1 diabetes participants without SFN (13.39 ± 4.66 ng/mL; p=0.11). Tear NPY levels were lower in individuals with type 1 diabetes and mild/moderate non-proliferative DR (10.44 ± 3.46 ng/mL) compared to none/minimal DR (13.79 ± 4.76 ng/mL; p=0.0005) and controls. In separate linear regression models, both the presence of SFN (ß = -0.75, p=0.02) and the presence of mild/moderate DR (ß = -0.84, p=0.009) were significantly associated with tear NPY levels relative to controls, after adjusting for participant age, sex, and dry eye disease. There were no inter-group differences for tear substance P concentrations.

CONCLUSIONS:

Tear NPY has potential utility as an indicator of peripheral microvascular complications associated with type 1 diabetes.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Ocul Surf Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Ocul Surf Year: 2024 Document type: Article