The American Journal of Medicine
Volume 114, Issue 4 , Pages 283-287, March 2003

Abnormal vitamin B6 status is associated with severity of symptoms in patients with rheumatoid arthritis

  • En-Pei I Chiang, PhD

      Affiliations

    • Vitamin Metabolism and Aging Laboratory (EIC, PJB, JS, MN), Jean Mayer USDA Human Nutrition Research Center on Aging, Tufts University, Boston, Massachusetts, USA
  • ,
  • Pamela J Bagley, PhD

      Affiliations

    • Vitamin Metabolism and Aging Laboratory (EIC, PJB, JS, MN), Jean Mayer USDA Human Nutrition Research Center on Aging, Tufts University, Boston, Massachusetts, USA
  • ,
  • Jacob Selhub, PhD

      Affiliations

    • Vitamin Metabolism and Aging Laboratory (EIC, PJB, JS, MN), Jean Mayer USDA Human Nutrition Research Center on Aging, Tufts University, Boston, Massachusetts, USA
  • ,
  • Marie Nadeau, MS

      Affiliations

    • Vitamin Metabolism and Aging Laboratory (EIC, PJB, JS, MN), Jean Mayer USDA Human Nutrition Research Center on Aging, Tufts University, Boston, Massachusetts, USA
  • ,
  • Ronenn Roubenoff, MD, MHS

      Affiliations

    • Nutrition, Exercise Physiology, and Sarcopenia Laboratory (RR), Jean Mayer USDA Human Nutrition Research Center on Aging, Tufts University, Boston, Massachusetts, USA
    • General Clinical Research Center (RR), New England Medical Center, Boston, Massachusetts, USA
    • Corresponding Author InformationRequests for reprints should be addressed to Ronenn Roubenoff, MD, MHS, Nutrition, Exercise Physiology, and Sarcopenia Laboratory, Jean Mayer USDA Human Nutrition Research Center on Aging, Tufts University, 711 Washington Street, Boston, Massachusetts 02111, USA

Received 16 January 2002; received in revised form 26 September 2002; accepted 8 October 2002.

Abstract 

Purpose

Patients with rheumatoid arthritis have low plasma vitamin B6 levels and elevated plasma homocysteine responses to a methionine load. We examined whether these abnormalities are associated with clinical and biochemical indicators of disease status.

Methods

We performed a cross-sectional study in 37 patients who met the American College of Rheumatology criteria for rheumatoid arthritis. Vitamin B6 status was assessed by the plasma pyridoxal 5′-phosphate level and with the homocysteine response to a methionine load test. Clinical disease activity was assessed by joint counts, the Health Assessment Questionnaire disability score, and biochemical markers of the acute phase response.

Results

Plasma pyridoxal 5′-phosphate levels were inversely correlated with the erythrocyte sedimentation rate (r = −0.37, P = 0.02), C-reactive protein level (r = −0.52, P = 0.002), disability score (r = −0.37, P = 0.02), morning stiffness (r = −0.38, P = 0.02), and degree of pain (r = −0.33, P = 0.04). The increase in homocysteine levels after a methionine load correlated with the erythrocyte sedimentation rate (r = 0.39, P = 0.02), C-reactive protein level (r = 0.37, P = 0.03), disability score (r = 0.37, P = 0.04), degree of pain (r = 0.38, P = 0.02) and fatigue (r = 0.42, P = 0.01), number of painful joints (r = 0.43, P = 0.007), and number of swollen joints (r = 0.32, P = 0.05).

Conclusion

Markers of vitamin B6 status are associated with disease activity and severity, synovial burden, and pain in patients with rheumatoid arthritis, raising the possibility that impaired vitamin B6 status in these patients is a result of inflammation.

Keywords:  Rheumatoid arthritis, Inflammation, Pyridoxal 5′-phosphate, Homocysteine, C-reactive protein, Erythrocyte sedimentation rate

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 This project was supported by the U.S. Department of Agriculture under cooperative agreement no. 58-1950-9-001. Any opinions, findings, conclusions, or recommendations expressed in this publication are those of the authors and do not necessarily reflect the view of the U.S. Department of Agriculture. This study was also supported in part by grant RR-00054 from the National Center for Research Resources, for the General Clinical Research Center, New England Medical Center, and Tufts University School of Medicine, and by an Arthritis Foundation Dissertation Award.

PII: S0002-9343(02)01528-0

doi:10.1016/S0002-9343(02)01528-0

The American Journal of Medicine
Volume 114, Issue 4 , Pages 283-287, March 2003