Association between changes in the mRNA expression of platelet-activating factor receptor in peripheral blood

Sahar Ghavidel Darestani1, Mihoko Kurano1, Atsushi Shinnakasu1

  • 1Department of Diabetes and Endocrine Medicine, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, 8-35-1, Sakuragaoka, Kagoshima, 890-8520 Japan.

Diabetology International
|January 18, 2020
PubMed
Abstract

Insights

Elevated platelet-activating factor receptor (PAFR) mRNA in PBMCs is linked to diabetic nephropathy progression, suggesting a common underlying mechanism. This association highlights potential pathways for diabetic complications.

Area of Science:

  • Endocrinology
  • Nephrology
  • Immunology

Background:

  • Inflammatory mediators play a role in diabetic complications.
  • Platelet-activating factor receptor (PAFR) mRNA expression in peripheral blood mononuclear cells (PBMCs) was previously linked to urinary albumin to creatinine ratio (ACR) and forearm flow-mediated dilatation in type 2 diabetes patients.

Purpose of the Study:

  • To elucidate the association between PAFR mRNA expression in PBMCs and diabetic nephropathy progression over a 1-year follow-up period.

Main Methods:

  • Recruited 95 type 2 diabetes patients, with 86 completing a 1-year follow-up.
  • Categorized patients into normoalbuminuria, microalbuminuria, and macroalbuminuria groups.
  • Measured baseline and 12-month characteristics, including gene expression of PAFR in PBMCs.

Main Results:

  • Higher baseline PAFR mRNA expression was observed in macroalbuminuria patients.
  • Changes in PAFR mRNA expression correlated with changes in ACR in all patients (r=0.225, p=0.037).
  • Changes in PAFR mRNA expression correlated with estimated glomerular filtration rate in macroalbuminuria patients (r=-0.438, p=0.047).

Conclusions:

  • No direct causal relationship was found between diabetic nephropathy and elevated PAFR expression in PBMCs.
  • The close association suggests a shared underlying mechanism contributing to both conditions.
  • The PAF/PAFR interaction may offer insights into mechanisms driving diabetic complications.