Platelet indices and inflammatory bowel disease: a Mendelian randomization study

Front Immunol. 2024 Jul 9:15:1377915. doi: 10.3389/fimmu.2024.1377915. eCollection 2024.

Abstract

Background: Platelets play a significant role in the innate and adaptive processes of immunity and inflammation. Inflammatory bowel disease (IBD) is an autoimmune disease that is widely understood to be caused by a combination of genetic predisposition, aberrant immune responses, etc.

Methods: To examine the relationships between genetically determined platelet indices and IBD, we conducted a Mendelian randomization (MR) study. Data associated with platelet count (PLT), mean platelet volume (MPV), platelet distribution width (PDW), plateletcrit (PCT) were used from the UK Biobank. The outcome data, including IBD, Crohn's disease (CD), ulcerative colitis (UC), were from the FinnGen database. The inverse variance-weighted (IVW), MR-Egger, weighted median methods were used for MR analyses.

Results: The MR estimations from the IVW approach show a significant connection between PLT and IBD. Similarly, PCT and IBD have a relationship following the IVW and MR-Egger approaches. While PLT and PCT have strong relationships with CD, according to the findings of all three approaches respectively. Nevertheless, PDW was the only relevant indicator of UC. The only significant result was IVW's.

Conclusion: Our findings suggest that the fluctuation of platelet indicators is of great significance in the development of IBD. PLT and PCT have a close association with IBD and CD, respectively; PDW only has a connection with UC. Platelets play an important role in the progression of IBD (UC, CD).

Keywords: Crohn’s disease; Mendelian randomization; inflammatory bowel disease; platelet indices; ulcerative colitis.

MeSH terms

  • Blood Platelets* / immunology
  • Crohn Disease / blood
  • Crohn Disease / genetics
  • Crohn Disease / immunology
  • Genetic Predisposition to Disease
  • Humans
  • Inflammatory Bowel Diseases* / blood
  • Inflammatory Bowel Diseases* / diagnosis
  • Inflammatory Bowel Diseases* / genetics
  • Mean Platelet Volume
  • Mendelian Randomization Analysis*
  • Platelet Count
  • Polymorphism, Single Nucleotide

Grants and funding

The authors declare financial support was received for the research, and/or publication of this article. This work was supported by the grants from National Key Research and Development Project of China (No. 2023YFC2413100).