AI Article Synopsis

  • The study investigated the relationship between iron and polyunsaturated fatty acid (PUFA) intake and diabetic peripheral neuropathy (DPN) among 147 individuals with type 2 diabetes using dietary records and a screening tool.
  • Findings indicated that individuals with DPN had significantly higher iron intake and a higher iron to PUFA ratio compared to those without DPN, suggesting a potential link between these dietary factors and DPN.
  • Logistic regression analysis revealed that both higher iron intake and a greater iron/PUFA ratio were associated with an increased likelihood of having DPN, highlighting the need for mindful dietary practices in managing type 2 diabetes.

Article Abstract

We aimed to investigate the association of iron and polyunsaturated fatty acid (PUFA) intake with diabetic peripheral neuropathy (DPN) in individuals with type 2 diabetes. This cross-sectional study included 147 individuals with type 2 diabetes. Dietary intake was assessed using three-day food records. DPN was diagnosed on the basis of a Michigan Neuropathy Screening Instrument-Physical Examination score ≥2.5. Adjusted for total energy intake, iron intake was significantly higher in individuals with DPN than in those without DPN (10.9 ± 4.0 mg vs. 9.9 ± 3.6 mg, = 0.041). In addition, the iron/PUFA ratio was significantly higher in individuals with DPN (1.4 ± 0.8 vs. 1.1 ± 0.4, = 0.005). Logistic regression analyses showed that iron intake (odds ratio (OR): 1.152; 95% confidence interval (CI): 1.012, 1.311) and iron/PUFA ratio (OR: 2.283; 95% CI: 1.066, 4.887) were associated with DPN after adjustment for total energy intake, sex, age, body mass index, systolic blood pressure, diabetes duration, estimated glomerular filtration rate, glycated hemoglobin, low-density lipoprotein cholesterol, and smoking. In conclusion, high dietary iron intake and an elevated iron/PUFA ratio were associated with the presence of DPN. The present study suggests the importance of the dietary pattern of iron and PUFA intake in individuals with type 2 diabetes.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7693683PMC
http://dx.doi.org/10.3390/nu12113365DOI Listing

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