Brain and Development
Volume 34, Issue 2 , Pages 92-97, February 2012

Diagnostic accuracy of blood and CSF lactate in identifying children with mitochondrial diseases affecting the central nervous system

  • Keitaro Yamada

      Affiliations

    • Department of Pediatric Neurology, Osaka Medical Center and Research Institute for Maternal and Child Health, Osaka, Japan
    • Corresponding Author InformationCorresponding author. Address: Department of Pediatric Neurology, Osaka Medical Center and Research Institute for Maternal and Child Health, 840 Murodo-cho, Izumi, Osaka 594-1101, Japan. Tel.: +81 725 56 1220; fax: +81 725 56 5682.
  • ,
  • Yasuhisa Toribe

      Affiliations

    • Department of Pediatric Neurology, Osaka Medical Center and Research Institute for Maternal and Child Health, Osaka, Japan
  • ,
  • Keiko Yanagihara

      Affiliations

    • Department of Pediatric Neurology, Osaka Medical Center and Research Institute for Maternal and Child Health, Osaka, Japan
  • ,
  • Toshiyuki Mano

      Affiliations

    • Department of Pediatric Neurology, Osaka Medical Center and Research Institute for Maternal and Child Health, Osaka, Japan
  • ,
  • Mikihiro Akagi

      Affiliations

    • Department of Pediatrics, Osaka University Graduate School of Medicine, Osaka, Japan
  • ,
  • Yasuhiro Suzuki

      Affiliations

    • Department of Pediatric Neurology, Osaka Medical Center and Research Institute for Maternal and Child Health, Osaka, Japan

Received 8 May 2011; received in revised form 26 July 2011; accepted 6 August 2011. published online 29 August 2011.

Abstract 

Objective: To determine the diagnostic accuracy of blood and cerebrospinal fluid (CSF) lactate and pyruvate concentrations in identifying children with mitochondrial diseases (MD) affecting the central nervous system (CNS). Methods: We studied lactate and pyruvate concentrations in paired samples of blood and CSF collected concurrently from 17 patients with MD (Leigh encephalomyelopathy 10, MELAS 5, Pearson disease 1, PDH deficiency 1) and those from control patients (n=49). Results: Although blood and CSF variables (lactate, pyruvate concentrations and lactate/pyruvate ratio) were significantly higher in the mitochondrial group than in the control group, there was considerable overlap of individual values between these two groups. The maximum value of the area under the receiver operating characteristic curve (AUC) was observed for the CSF lactate concentration (0.994, optimal cut-off value 19.9mg/dl, sensitivity 0.941 and specificity 1.00), followed by the CSF pyruvate level (0.983). There was an inverse relationship between blood lactate and lactate CSF/blood ratio. For blood lactate concentrations between 20 and 40mg/dl, a significant difference was also noted in the lactate CSF/blood ratio between the two groups (AUC 1.0, optimal cut-off value 0.91, sensitivity 1.0 and specificity 1.0). Conclusions: Our study suggests that that CSF lactate level>19.9mg/dl is the most reliable variable for identifying patients with MD affecting the CNS. When blood lactate concentrations are marginally elevated (20–40mg/dl), lactate CSF/blood ratio>0.91 may also provide diagnostic information.

Keywords: Mitochondrial disorders, Cerebrospinal fluid, Lactate, Pyruvate, Children

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PII: S0387-7604(11)00213-0

doi:10.1016/j.braindev.2011.08.004

Brain and Development
Volume 34, Issue 2 , Pages 92-97, February 2012