Systemic inflammatory mediators and bone homeostasis in intestinal failure

JPEN J Parenter Enteral Nutr. 2007 Mar-Apr;31(2):142-7. doi: 10.1177/0148607107031002142.

Abstract

Background: A proinflammatory state has been described in patients with intestinal failure. The prevalence of metabolic bone disease in this group is considerable. It is not known whether this proinflammatory state is related to bone parameters, though bone disease is recognized as a proinflammatory process in postmenopausal women. The purpose of this study was to examine whether inflammation was related to bone disease.

Methods: Eight patients with parenteral nutrition (PN)-dependent intestinal failure but no recent infections or immunosuppressive medications had serum assayed for interleukin-6 (IL-6), tumor necrosis factor (TNF)-alpha, and its receptors (TNFR-I and TNFR-II), C-reactive protein, and whole blood for lymphocyte proliferation. Routine clinical laboratory measures of vitamin D, parathyroid hormone, serum calcium, and phosphorus within 3 months of the inflammatory measures were compared by Pearson's correlation to the inflammatory measures.

Results: Mean values for calcium, phosphorus, and albumin were normal, but 25-hydroxy vitamin D was reduced and parathyroid hormone and alkaline phosphatase elevated. Serum total calcium was negatively related to TNFR-II, TNF-alpha and positively to T-helper cells. Longer PN dependence was associated with inflammation and negatively with T-helper cells.

Conclusions: These preliminary findings are hypothesis generating only but support an association of low calcium and longer duration of PN with inflammation in patients with intestinal failure. Whether the inflammation results from vitamin D deficiency or the vitamin D deficiency develops secondary to excessive use of activated vitamin D to modulate inflammation from some other cause, such as a component of PN or repeated infectious challenge, requires further study.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Bone Diseases, Metabolic / blood
  • Bone Diseases, Metabolic / epidemiology
  • Bone Diseases, Metabolic / etiology*
  • Bone Diseases, Metabolic / immunology
  • Bone and Bones / metabolism*
  • Calcium / blood
  • Female
  • Humans
  • Inflammation Mediators / blood
  • Inflammation Mediators / metabolism
  • Intestinal Diseases / immunology
  • Intestinal Diseases / physiopathology
  • Intestinal Diseases / therapy*
  • Male
  • Middle Aged
  • Parathyroid Hormone / blood
  • Parenteral Nutrition, Home / adverse effects*
  • T-Lymphocytes
  • Vitamin D / analogs & derivatives
  • Vitamin D / blood*
  • Vitamin D Deficiency / etiology*
  • Vitamin D Deficiency / immunology
  • Vitamin D Deficiency / physiopathology

Substances

  • Inflammation Mediators
  • Parathyroid Hormone
  • Vitamin D
  • 25-hydroxyvitamin D
  • Calcium