PT  - JOURNAL ARTICLE
AU  - Cheong, Ian
AU  - Deelchand, Dinesh K
AU  - Eberly, Lynn E
AU  - Marjańska, Małgorzata
AU  - Manousakis, Georgios
AU  - Guliani, Gaurav
AU  - Walk, David
AU  - Öz, Gülin
TI  - Neurochemical correlates of functional decline in amyotrophic lateral sclerosis
AID  - 10.1136/jnnp-2018-318795
DP  - 2019 Mar 01
TA  - Journal of Neurology, Neurosurgery & Psychiatry
PG  - 294--301
VI  - 90
IP  - 3
4099  - http://jnnp.bmj.com/content/90/3/294.short
4100  - http://jnnp.bmj.com/content/90/3/294.full
SO  - J Neurol Neurosurg Psychiatry2019 Mar 01; 90
AB  - Objective To determine whether proton magnetic resonance spectroscopy (1H-MRS) can detect neurochemical changes in amyotrophic lateral sclerosis (ALS) associated with heterogeneous functional decline.Methods Nineteen participants with early-stage ALS and 18 age-matched and sex ratio-matched controls underwent ultra-high field 1H-MRS scans of the upper limb motor cortex and pons, ALS Functional Rating Scale-Revised (ALSFRS-R total, upper limb and bulbar) and upper motor neuron burden assessments in a longitudinal observational study design with follow-up assessments at 6 and 12 months. Slopes of neurochemical levels over time were compared between patient subgroups classified by the rate of upper limb or bulbar functional decline. 1H-MRS and clinical ratings at baseline were assessed for ability to predict study withdrawal due to disease progression.Results Motor cortex total N-acetylaspartate to myo-inositol ratio (tNAA:mIns) significantly declined in patients who worsened in upper limb function over the follow-up period (n=9, p=0.002). Pons glutamate + glutamine significantly increased in patients who worsened in bulbar function (n=6, p<0.0001). Neurochemical levels did not change in patients with stable function (n=5–6) or in healthy controls (n=14–16) over time. Motor cortex tNAA:mIns and ALSFRS-R at baseline were significantly lower in patients who withdrew from follow-up due to disease progression (n=6) compared with patients who completed the 12-month scan (n=10) (p<0.001 for tNAA:mIns; p<0.01 for ALSFRS-R), with a substantially larger overlap in ALSFRS-R between groups.Conclusion Neurochemical changes in motor areas of the brain are associated with functional decline in corresponding body regions. 1H-MRS was a better predictor of study withdrawal due to ALS progression than ALSFRS-R.