ORCID: https://orcid.org/0000-0002-2050-093X; Saito, Yoshiro
ORCID: https://orcid.org/0000-0002-0559-5889; Spagnuolo, Maria C.
ORCID: https://orcid.org/0009-0003-3228-8766; Maalmi, Haifa
ORCID: https://orcid.org/0000-0002-2910-1142; Shimizu, Misaki; Bönhof, Gidon J.
ORCID: https://orcid.org/0000-0003-1446-6592; Suzuki, Keita
ORCID: https://orcid.org/0000-0003-2833-4080; Rathmann, Wolfgang
ORCID: https://orcid.org/0000-0001-7804-1740; Peters, Annette
ORCID: https://orcid.org/0000-0001-6645-0985; Roden, Michael
ORCID: https://orcid.org/0000-0001-8200-6382; Ziegler, Dan
ORCID: https://orcid.org/0000-0001-8956-3552; Thorand, Barbara
ORCID: https://orcid.org/0000-0002-8416-6440 und Takamura, Toshinari
ORCID: https://orcid.org/0000-0002-4393-3244
(2024):
Differential associations between selenoprotein P and distal sensorimotor polyneuropathy in people with and without diabetes: KORA F4/FF4 study.
In: Free Radical Biology and Medicine, Bd. 223: S. 87-95
[PDF, 1MB]

Abstract
Background: Oxidative stress is a risk factor for distal sensorimotor polyneuropathy (DSPN). Selenoprotein P is a protein with antioxidant properties but has not been investigated in the context of DSPN. This study aimed to assess the associations between selenoprotein P and DSPN in people without and with type 2 diabetes (T2D).
Methods: Cross-sectional and prospective analyses were based on 1053 (including 217 with T2D) and 513 participants (including 79 with T2D), respectively, aged 61–82 years from the population-based KORA F4 survey. DSPN at baseline (KORA F4) and in the follow-up survey KORA FF4 was defined based on the Michigan Neuropathy Screening Instrument. Serum levels of full-length selenoprotein P were quantified by ELISA. Associations between selenoprotein P and prevalent or incident DSPN were estimated using logistic regression analysis adjusting for multiple confounders.
Results: Selenoprotein P levels were not associated with prevalent DSPN in the total sample. However, there was a significant interaction by diabetes status. Higher levels of selenoprotein P were associated with lower odds of prevalent DSPN in individuals without T2D (fully adjusted model: OR 0.825 [95 % CI 0.682, 0.998], p = 0.0476), but not in those with T2D (OR [95 % CI] 1.098 [0.829, 1.454], p = 0.5132; pinteraction = 0.0488). Selenoprotein P levels were not associated with incident DSPN over a follow-up of 6.5 years.
Conclusion: In individuals without T2D from the older general population, lower selenoprotein P levels were associated with a higher prevalence of DSPN. Whether the antioxidant properties of selenoprotein P are responsible for the observed associations remains to be elucidated in future research.
Dokumententyp: | Zeitschriftenartikel |
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Publikationsform: | Publisher's Version |
Keywords: | Biomarker ; Distal sensorimotor polyneuropathy ; Reductive stress ; Selenoprotein P ; Oxidative stress ; Antioxidant |
Fakultät: | Medizin > Institut für Medizinische Informationsverarbeitung, Biometrie und Epidemiologie |
Themengebiete: | 600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin und Gesundheit |
URN: | urn:nbn:de:bvb:19-epub-124414-3 |
ISSN: | 08915849 |
Sprache: | Englisch |
Dokumenten ID: | 124414 |
Datum der Veröffentlichung auf Open Access LMU: | 24. Feb. 2025 14:47 |
Letzte Änderungen: | 24. Feb. 2025 14:47 |