4.6 Article

Homocysteine-Lowering Therapy or Antioxidant Therapy for Bone Loss in Parkinson's Disease

Journal

MOVEMENT DISORDERS
Volume 25, Issue 3, Pages 332-340

Publisher

WILEY
DOI: 10.1002/mds.22866

Keywords

folate; homocysteine; osteoporosis; Parkinson's disease; vitamin B-12

Funding

  1. Korean Ministry of Education, Science and Technology [FPROSB1-170]
  2. 21C Frontier Functional Proteomics Program
  3. Korea Healthcare Technology RD Project
  4. Ministry for Health, Welfare and Family Affairs, Republic of Korea [A080256]
  5. Ministry of Health and Welfare, Republic of Korea [A080256, A010252, 01-PJ10-PG6-01GN15-0001]
  6. Asan Institute for Life Sciences, Seoul, Korea [2008-026, 2008-347]
  7. Korean Ministry of Science and Technology (MOST)
  8. Korea Science and Engineering Foundation
  9. Korean Ministry of Education. Science and Technology [FPR08B1-170]
  10. Korea Health Promotion Institute [A080256] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  11. Korea Institute of Industrial Technology(KITECH) [2008-026] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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We investigated whether homocysteine (Hcy)lowering therapy or an antioxidant prevented bone loss in Parkinson's disease (PD) patients taking levodopa. Forty-two PD patients with low bone mineral density (BMD) taking levodopa were randomly assigned to Hcy-lowering therapy (5 mg folate and 1500 mu g vitamin B-12 daily), alpha-lipoic acid (alpha-LA) therapy (1200 mg daily), or control groups. Primary outcomes were BMD changes from baseline to 12 months. Secondary outcomes were changes in Hey level, and C-telopeptide (CTX) levels at 12 months. Forty-one patients completed the study. Hcy-lowering therapy resulted in significantly greater BMD changes at the lumbar spine (4.4%), total femur (2.8%), and femur shaft (2.8%) than control (P = 0.005-0.023). BMD changes in the alpha-LA therapy group were similar to those of the control group, but changes at the trochanter (4.6%) were significantly greater in the alpha-LA therapy group than in the control group after adjustment for body mass index changes. Hey concentrations decreased to 35.2% +/- 13.4% in the Hcy-lowering therapy group, but increased in other groups. Serum CTX levels at 12 months tended to be lower in the Hcy-lowering group (0.442 +/- 0.024 ng/mL) than control group (0.628 +/- 0.039 ng/mL) (P = 0.159). This small trial suggests that Hcy-lowering therapy may prevent bone loss in PD patients taking levodopa. (C) 2009 Movement Disorder Society

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