Stress lactate in mitochondrial myopathy under constant, unadjusted workload
Authors:
- 7 December 2004
- journal article
- research article
- Published by Wiley in European Journal of Neurology
- Vol. 11 (12) , 811-816
Abstract
As it is under debate if determination of lactate during cycle ergometry (lactate stress testing, LST) under a continuous, unadjusted, low workload is a valuable diagnostic tool for mitochondrial myopathy (MMP), the present study aimed to investigate how sensitive the LST is in a large cohort of patients with indications for MMP (MMP patients). Serum lactate was determined once before, three times during, and once after a 15‐min, constant 30 W‐workload on a bicycle ergometer in 115 healthy controls, 166 patients with neurological disorders other than MMP, and 291 MMP patients. Serum lactate's upper reference limit at rest, 5, 10, 15 min after starting, and 15 min after finishing the exercise was 2.0, 2.0, 2.1, 2.0 and 1.7 mmol/l, respectively. Resting lactate was increased in 75 MMP patients (26%). The specificity of resting lactate determination was 84%. The sensitivity of the LST was 66% and the specificity 84%. Among the 192 MMP patients with abnormal LST, 120 (63%) had a normal resting lactate. The LST is abnormal in two thirds of the MMP patients. The sensitivity of the LST is higher than that of resting lactate determination. The LST is a simple and cheap but effective and reliable screening method for detecting the impaired oxidative metabolism in MMP.Keywords
This publication has 16 references indexed in Scilit:
- Cycle ergometry is not a sensitive diagnostic test for mitochondrial myopathyJournal of Neurology, 2003
- Lactate Stress Testing in 155 Patients with MitochondriopathyCanadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques, 2002
- Diagnostic yield of the lactate stress test in respiratory chain disorders under absolute and relative workloadJournal of Neuroscience Methods, 2001
- Diagnostic yield of the lactate stress test in 160 patients with suspected respiratory chain disorderMetabolic Brain Disease, 2000
- Lactate as a fuel for mitochondrial respirationActa Physiologica Scandinavica, 2000
- Standardisierte aerobe Gehbelastung auf dem Laufband bei Gesunden sowie Patienten mit mitochondrialen und nichtmitochondrialen MyopathienDer Nervenarzt, 1997
- Exercise fuel mobilization in mitochondrial myopathy: A metabolic dilemmaAnnals of Neurology, 1996
- Mitochondrial DiseaseChest, 1995
- Presentation and clinical investigation of mitochondrial respiratory chain disease. A study of 51 patientsBrain, 1995
- Biochemical and molecular features of deficiencies of Complexes I, II and III1994