Authors
Jessica Paola Loaiza-Giraldo, Rocío Valdivia-Arroyo, Valentina Greve-Quezada, Alonso Quivira-Muñoz, Orlando Silva-Perez, Trinidad Soublette-Tocornal, Alejandro Bruna-Mejias, Pablo Nova-Baeza, Mathias Orellana-Donoso, Maria P Moya, Juan Sanchis-Gimeno, Vitor E Valenti, Maria Piagkou, Marko Konschake, Juan José Valenzuela-Fuenzalida
Published in
Current developments in nutrition. Volume 10. Issue 8. Pages 109439. Epub Jul 18, 2026.
Abstract
Omega-3 (n-3) polyunsaturated fatty acids, including marine-derived eicosapentaenoic acid and docosahexaenoic acid, as well as plant-derived formulations rich in α-linolenic acid, have been proposed as adjunctive therapy in diabetes because of their potential effects on lipid metabolism, inflammation, oxidative stress, and neuroprotection. Searches were performed in MEDLINE, EMBASE, SCOPUS, Cochrane Central Register of Controlled Trials, Cumulative Index to Nursing and Allied Health Literature, and Web of Science through January 2026. Outcomes included lipid parameters, glycemic markers, inflammatory and oxidative stress biomarkers, and corneal nerve branch density (CNBD). Random-effects models were applied. Eleven trials met the criteria for quantitative synthesis. Pooled analyses showed no significant effects on triglycerides, low-density or high-density lipoprotein cholesterol, glycated hemoglobin, fasting plasma glucose, or inflammatory and oxidative stress biomarkers, with substantial heterogeneity across several outcomes. In contrast, fasting insulin and homeostasis model assessment of insulin resistance were significantly reduced with low heterogeneity, and CNBD showed a consistent improvement with no detectable heterogeneity, suggesting potential benefits for insulin sensitivity and small-fiber nerve integrity. Overall, the certainty of evidence ranged from very low to low, mainly because of heterogeneity, imprecision, and small sample sizes. ω-3 supplementation demonstrated limited effects on most metabolic and inflammatory outcomes in diabetes. Observed improvements in insulin sensitivity indices and CNBD warrant further investigation in adequately powered trials with longer follow-up. These findings should be interpreted as hypothesis-generating rather than confirmatory.
PMID:
42602626
Bibliographic data and abstract were imported from PubMed on 15 Aug 2026.
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