4.6 Article

Plasma homocysteine, apolipoprotein E status and vascular disease in elderly patients with mental illness

Journal

CLINICAL CHEMISTRY AND LABORATORY MEDICINE
Volume 48, Issue 1, Pages 129-135

Publisher

WALTER DE GRUYTER GMBH
DOI: 10.1515/CCLM.2010.013

Keywords

apolipoprotein E; cobalamin; creatinine; folate; homocysteine; psychogeriatric patients; vascular disease

Funding

  1. Swedish Medical Research Council [3950]
  2. Alzheimer Foundation Sweden
  3. Sjobring Foundation
  4. Swedish Heart Lung Foundation
  5. Albert Pahlsson Foundation
  6. County Council of Malmohus

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Background: Total plasma homocysteine (tHcy) concentration is increased in elderly patients with mental illness. Also, patients with vascular disease have significantly higher plasma tHcy concentration compared with patients without vascular disease. Apolipoprotein E (apoE) status is associated with cardiovascular disease and a major genetic risk factor is inheritance of the e4 allele. In the present study, we investigated the association between plasma tHcy and apoE status. Methods: The relation between apoE status, plasma tHcy and vascular disease was investigated in a cohort of consecutively enrolled elderly patients with mental illness (n=328). Results: Plasma tHcy concentrations were increased (p<0.01) in carriers of APOE4 (13.6 mu mol/L; 9.2-21.7 mu mol/L) compared to non-carriers (12.4 mu mol/L; 8.3-19.9 mu mol/L). The proportion of patients with vascular disease was significantly (p<0.001) increased among carriers (61%) compared to non-carriers (42%). An increased percentage (p<0.001) of APOE4 carriers was observed in patients with Alzheimer's disease (AD) with (71%) or without vascular disease (42%), and in patients with vascular dementia (VaD) (54%) compared to a reference group (34%). Conclusions: Since carriers of APOE4 showed an increased likelihood of vascular disease, these patients need more intensive control of other modifiable vascular risk factors. Furthermore, the association between plasma tHcy and the presence of APOE4 might be attributed to an increased proportion of vascular disease in APOE4 carriers. Clin Chem Lab Med 2010; 48: 129-35.

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