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The importance of identifying PsO patients at elevated risk of progressing to PsA arises from the observed disparity in treatment efficacy vs cutaneous signs, wherein fewer than 50% of patients achieve clinical remission once PsA has been established.4 These circumstances drive research into the feasibility of preventing PsA development or intercepting its progression.5 Given the established correlation between PsO severity and PsA risk,3 several investigations have explored the prospect of aggressive systemic therapies, such as biologic therapies, as potential preventive measures vs PsA development.1,613 In the current landscape, biologic therapies represent some of the most effective therapies for PsO

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To search for oxidative stress-related DCD studies, we employed the following search terms: TS= (diabetic cognitive impairment or diabetic cognitive dysfunction) AND TS=oxidative stress

Rats given BPC-157 after ligament injuries showed faster recovery and improved tissue quality
