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Letters to the Editor |
1 Centre de Recerca Biomèdica, Hospital Universitari de Sant Joan, Institut de Recerca en Ciències, de la Salut, Reus, Catalunya, Spain
2 University Department of Medicine, Manchester Royal Infirmary, Manchester, United Kingdom
aAddress correspondence to this author at: Centre de Recerca Biomèdica, Hospital Universitari de Sant Joan, Institut de Recerca en Ciències de la Salut, C/. Sant Joan s/n, 43201-Reus, Catalunya, Spain. Fax 34-977-312569; e-mail jcamps@grupsagessa.com.
| The first 20% of the full text of this article appears below. |
To the Editor:
Paraoxonase 1 (PON1) is a HDL-associated enzyme that catalyzes the hydrolysis of lipid peroxides in LDL and HDL and has been postulated as a member of the plasma antioxidant system. Decreased PON1 activity has been associated with atherosclerosis in persons with diabetes mellitus, familial hypercholesterolemia, and renal disease (1)(2).
Serum is the preferred sample for PON1 measurement because this enzyme requires calcium for both activity and stability. The presence of calcium chelators such as EDTA or citrate as anticoagulants inhibits PON1 activity (3). This is a serious limitation in retrospective studies, in which serum is not always available. Moreover, in studies on experimental animals, in which the amount of blood collected is often minimal, it is more convenient to use anticoagulants because the recovery of plasma is generally higher than that of serum and there is no interference by the clotting process.
Lithium heparin is an anticoagulant
The following articles in journals at HighWire Press have cited this article:
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M. M. Murphy, J. Marsillach, J. Camps, J. Fernandez-Ballart, B. Mackness, M. Mackness, N. Ferre, and J. Joven Influence of PON1 Polymorphisms on the Association between Serum Paraoxonase 1 and Homocysteinemia in a General Population. Clin. Chem., April 1, 2006; 52(4): 781 - 782. [Full Text] [PDF] |
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