Paper Details 
Original Abstract of the Article :
OBJECTIVES: To investigate the effects of salsalate on fasting and postprandial (PP) glycemic, lipidemic, and inflammatory responses in persons with tetraplegia. METHODS: This study was a randomized, double-blind, cross-over design. It was conducted at a university laboratory. Ten males aged 25 to ...See full text at original site
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引用元:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10644859/

データ提供:米国国立医学図書館(NLM)

Salsalate: A Potential Solution for Postprandial Glycemic Control in Tetraplegia?

Individuals with tetraplegia often face challenges in managing their blood sugar levels, especially after meals. This study investigates the potential of salsalate, a nonsteroidal anti-inflammatory drug, in improving postprandial glycemic control and lipid responses in individuals with tetraplegia. The researchers conducted a randomized, double-blind, crossover trial to assess the effects of salsalate on metabolic parameters.

Salsalate: A Potential Ally in Managing Postprandial Glycemia

The study found that salsalate significantly reduced both fasting and postprandial glucose levels in individuals with tetraplegia, suggesting a potential benefit in managing postprandial glycemic control. However, the study was relatively small, and further research is needed to confirm these findings.

Exploring New Approaches for Managing Blood Sugar in Tetraplegia

This research underscores the importance of exploring new approaches for managing blood sugar levels in individuals with tetraplegia. Salsalate, while requiring further investigation, holds potential as a promising tool for improving metabolic health in this population.

Dr.Camel's Conclusion

This study, like a refreshing oasis in the desert, offers hope for better blood sugar management in individuals with tetraplegia. Salsalate, a potential new tool in the desert of metabolic control, encourages further exploration of its role in improving health outcomes for this population.

Date :
  1. Date Completed n.d.
  2. Date Revised 2023-12-11
Further Info :

Pubmed ID

38076289

DOI: Digital Object Identifier

PMC10644859

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Languages

English

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