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The loss of 5-methyltetrahydrofolate in human serum under suboptimal preanalytical conditions can only partially be recovered by an oxidation product.
Fazili, Zia; Sternberg, Maya R; Paladugula, Neelima; Whitehead, Ralph D; Chen, Huiping; Pfeiffer, Christine M.
Afiliação
  • Fazili Z; National Center for Environmental Health, Centers for Disease Control and Prevention, Atlanta, GA.
  • Sternberg MR; National Center for Environmental Health, Centers for Disease Control and Prevention, Atlanta, GA.
  • Paladugula N; National Center for Environmental Health, Centers for Disease Control and Prevention, Atlanta, GA.
  • Whitehead RD; National Center for Environmental Health, Centers for Disease Control and Prevention, Atlanta, GA.
  • Chen H; National Center for Environmental Health, Centers for Disease Control and Prevention, Atlanta, GA.
  • Pfeiffer CM; National Center for Environmental Health, Centers for Disease Control and Prevention, Atlanta, GA cpfeiffer@cdc.gov.
J Nutr ; 144(11): 1873-9, 2014 Nov.
Article em En | MEDLINE | ID: mdl-25332487
BACKGROUND: Maintaining folate stability during sample handling is important, yet challenging. OBJECTIVE: We investigated the effects of suboptimal preanalytical conditions on serum folate stability. METHODS: By using an HPLC-tandem MS method we measured folates [5-methyltetrahydrofolate (5-methylTHF), folic acid, MeFox (5-methylTHF oxidation product, pyrazino-s-triazine derivative of 4α-hydroxy-5-methylTHF), and other minor folate forms at or below the limit of detection] in human serum exposed to suboptimal conditions. RESULTS: Whole blood samples (n = 21) stored at 32°C for ≤ 3 d (Expt. 1: delayed processing) showed significant decreases in serum total folate (tFOL; sum of folate forms: 11-32%, 5.5-15.9 nmol/L) and 5-methylTHF (36-62%, 14.5-25.1 nmol/L) and a significant increase in MeFox (346-415%, 7.17-8.63 nmol/L). Serum samples (n = 21) stored at 11°C for 7-14 d (Expt. 2: delayed freezing) also showed significant decreases in tFOL (4.6-10.4%, 2.3-5.1 nmol/L) and 5-methylTHF (8.4-29%, 3.4-11.6 nmol/L) and significant increases in MeFox (88-320%, 1.82-6.62 nmol/L). The molar loss in 5-methylTHF exceeded the gain in MeFox in these 2 experiments. When we exposed 3 serum pools (tFOL: 16.7-58.3 nmol/L) for 24 h to an elevated temperature of 37°C (Expt. 3), the significant decrease in 5-methylTHF (33% on average) was compensated for by an equimolar gain in MeFox. Repeated freeze/thaw cycles (≤ 3 cycles) of serum [closed (Expt. 4) and open (Expt. 5) vials] showed generally stable folates with small (<1 nmol/L) changes. Long-term (≤ 12 mo) exposure of 3 serum pools (tFOL: 17.5-63.7 nmol/L) to a suboptimal (-20°C) freezing temperature (Expt. 6) showed significant decreases in tFOL (5% on average) already after 3 mo. The molar loss in 5-methylTHF exceeded the gain in MeFox. Folic acid generally showed good stability. CONCLUSIONS: To avoid folate losses, unprocessed whole blood should be protected from elevated temperatures and serum should not be refrigerated for >2 d or for a long term stored at -20°C.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Coleta de Amostras Sanguíneas / Tetra-Hidrofolatos Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: J Nutr Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Coleta de Amostras Sanguíneas / Tetra-Hidrofolatos Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: J Nutr Ano de publicação: 2014 Tipo de documento: Article