Elevated platelet counts in a cohort of children with moderate-severe osteogenesis imperfecta suggest that inflammation is present

Arch Dis Child. 2018 Aug;103(8):767-771. doi: 10.1136/archdischild-2017-313859. Epub 2018 Mar 13.

Abstract

Background: Elevated platelet counts are observed in cancer, autoimmunity and inflammation with concurrent illness. Proinflammatory cytokines are elevated in murine osteogenesis imperfecta (OI) models. We hypothesised that platelet counts might be elevated in children with moderate-severe OI.

Methods: We reviewed the hospital records of 71 children with moderate-severe OI, treated in the Sheffield Children's Hospital's Severe, Complex and Atypical Osteogenesis Imperfecta Highly Specialised Service. Data relating platelet count (below/above average, above upper limit) to prior and concurrent events were summarised as event proportions per child. Additionally, we created platelet SD scores to assess age and time-related trends, and relationship with OI type.

Results: 1206 platelet counts were recorded. Platelet SD scores were right-shifted by 0.89 SD overall. 49 of 71 (69%) patients had at least one platelet count above the normal range and 246 (20.4%) of all counts were above the upper limit of normal. Of these, 101 (41%) were high despite no confounding factors being present. For the 47 children with data at age less than 2 years, 89 (30.0%) platelet counts were above the upper limit of normal and 39 (44%) had no associated confounding factor. Elevated platelet counts were recorded most often for children with new or existing vertebral fractures.

Conclusions: Raised platelet counts were observed in association with new and healing vertebral fractures, but also (41%-44%) in the absence of identified proinflammatory factors or events. We speculate that these findings are evidence for a proinflammatory component to OI that could be a target for therapeutic intervention.

Keywords: bone disease; collagen disorders; musculo-skeletal.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Biomarkers / blood
  • Bone Density Conservation Agents / therapeutic use
  • Child
  • Child, Preschool
  • Female
  • Fracture Healing / physiology
  • Humans
  • Infant
  • Infant, Newborn
  • Inflammation / blood
  • Male
  • Osteogenesis Imperfecta / blood*
  • Osteogenesis Imperfecta / drug therapy
  • Osteogenesis Imperfecta / physiopathology
  • Platelet Count
  • Retrospective Studies
  • Spinal Fractures / blood
  • Spinal Fractures / etiology
  • Spinal Fractures / physiopathology
  • Thrombocytosis / etiology*

Substances

  • Biomarkers
  • Bone Density Conservation Agents