RS3PE Syndrome with Subsequent PMR Caused by Long-Term DPP-4 Inhibitor Use

Yuichi Takahashi1, Gautam A Deshpande1, Yoshinori Kanai1

  • 1Department of General Medicine, Juntendo University Faculty of Medicine, Tokyo, Japan.

Insights

Dipeptidyl peptidase-4 inhibitors (DPP-4i) like vildagliptin may cause Remitting seronegative symmetrical synovitis with pitting oedema (RS3PE) syndrome and polymyalgia rheumatica (PMR). These rare conditions cause painful extremities and warrant investigation for drug side effects.

Area of Science:

  • Rheumatology
  • Endocrinology
  • Pharmacology

Background:

  • Remitting seronegative symmetrical synovitis with pitting oedema (RS3PE) syndrome is a rare condition.
  • Dipeptidyl peptidase-4 inhibitors (DPP-4i) are commonly used for type 2 diabetes management.
  • Previous reports suggest a link between DPP-4i and RS3PE syndrome.

Purpose of the Study:

  • To report a case of RS3PE syndrome and polymyalgia rheumatica (PMR) in a patient using vildagliptin, a DPP-4i.
  • To highlight the potential for DPP-4i to cause these rare rheumatological conditions.
  • To emphasize the importance of considering drug side effects in the differential diagnosis.

Main Methods:

  • Case report of a 73-year-old male with type 2 diabetes.
  • Observation of RS3PE syndrome and PMR development during vildagliptin treatment.
  • Review of literature on DPP-4i associated rheumatological adverse events.

Main Results:

  • The patient developed RS3PE syndrome as a side effect of vildagliptin.
  • The patient subsequently developed polymyalgia rheumatica (PMR), a novel association with long-term DPP-4i use.
  • This case expands the known spectrum of DPP-4i-induced rheumatological complications.

Conclusions:

  • RS3PE syndrome and PMR are rare causes of painful extremities.
  • The potential association between DPP-4i and these conditions requires further investigation.
  • Drug-induced side effects should be considered in the differential diagnosis of RS3PE syndrome and PMR, alongside malignancy and giant cell arteritis.

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