Cell Signaling, Reinnervation and Metabolism in Kennedy Disease and Amyotrophic Lateral Sclerosis (ALS)

In amyotrophic lateral sclerosis (ALS), loss of functional motor neurons is initially compensated for by collateral reinnervation but, as the disease progresses, compensation usually fails leading to progressive muscle weakness. Conversely, in long-term ALS survivors, slow functional decline is correlated with their ability to maintain a successful compensatory response to denervation over time. The molecular mechanisms by which compensatory reinnervation, a crucial process for function and survival, is maintained over time remains to be elucidated. We have previously shown that muscle factors may be involved in maintenance of muscle innervation and function in ALS long-term survivors (Bruneteau et al.,2013). Energy metabolism and glucose homeostasis modifications also influence disease clinical course but the mechanisms by which they contribute to ALS progression are unknown. Insulin signaling cascades share many common steps with Insulin-like Growth Factor-1 (IGF-1) signaling pathways, and link maintenance of muscle mass with glucose and energy metabolism which are both connected to ALS progression. Our working hypothesis is that insulin signaling pathways play a major role in maintaining collateral reinnervation and muscle function in ALS. To comfort this hypothesis, we will quantify innervation in muscle specimens obtained from ALS patients and correlate these results to the level of activation of insulin main signaling pathways and expression of key determinants of glucose metabolism. These data will be analyzed together with evaluation of motor function and motor neuron loss over time, to understand how insulin signaling and glucose homeostasis influence disease progression. To decipher how energy and glucose metabolism are involved in preservation of a high level of collateral reinnervation over time, results obtained in ALS patients will be compared to those of normal subjects of similar age and patients with spinal and bulbar muscular atrophy (SBMA). PATIENTS EVALUATION 1. Clinical evaluation * Characteristics of patients * Patient characteristics will be reviewed at the time of inclusion: personal or familial history of medical conditions, age at onset, localization of onset (limb or bulbar), concomitant medications including riluzole. * Disease evaluation will be performed at baseline, 3 months, 6 months and 12 months: * Functional impairment will be assessed using the revised ALS Functional Rating Scale (ALSFRS-R), a 12-item scale that rates the performance of activities of daily living. Signs and symptoms range from 4 (normal function) to 0 (unable to attempt the task) (Cedarbaum et al.,1999). Twelve functions are listed, including: speech, salivation and swallowing for bulbar involvement; writing, feeding, dressing, turning in bed, walking and climbing stairs for upper and lower limbs involvement; respiratory function. * Muscle strength will be measured on 28 muscles by manual muscle testing according to the grading system of the Medical Research Council. 2. Laboratory tests * The routine biological tests, including platelet count and coagulation test will be performed at baseline * For all patients, genetic screening of all major ALS-associated genes will be performed at the time of inclusion (including C9ORF72, SOD1, TARDBP, FUS, UBQLN2, TBK1 genes to date and any novel major ALS-linked gene that could be discovered). * Respiratory function will be assessed at baseline, M6 and M12 as part of the routine follow-up procedure in the ALS center, including vital capacity expressed as a percentage of the predicted normal vital capacity, arterial blood gas analysis for determination of partial pressure of arterial oxygen and carbon dioxide, and nocturnal pulse oximetry (oxyhemoglobin saturation). 3. Surface EMG procedure and motor unit number index (MUNIX) measurement Surface EMG evaluation of neuromuscular function will be performed in all patients at baseline. The standardized EMG protocol will include motor nerve conduction studies of upper and lower limbs, and repetitive nerve stimulation studies for assessment of neuromuscular transmission on the spinal accessory nerve, the axillary nerve, the ulnar nerve and the radial nerve of both upper limbs. MUNIX measurement will be performed on deltoid and biceps brachii muscles, at baseline, 3 months, 6 months and 12 months. 4. Assessment of nutritional status and general metabolic profile Assessment of nutritional status and general metabolic profile will be performed at baseline for the two groups of patients and will include: * Data collection for weight, height, BMI determination, waist and hip circumference (waist/hip ratio calculation), nutrient intake * Measurements of body composition with whole body Dual X-Ray Absorptiometry (DEXA) * Assessment of resting energy expenditure (indirect calorimetry) * Evaluation of insulin secretion and insulin resistance with measurement of glucose and insulin levels before and 30 mn after ingestion of a standardized liquid meal test. Insulin resistance and insulin secretion will be evaluated by calculation of HOMA-IR (insulin resistance index) and insulin secretion will be evaluated by calculation of HOMA-B (insulin secretion index) and insulinogenic index. * Determination of serum concentrations of IGF-1 axis components. MOTOR-POINT MUSCLE BIOPSY PROCEDURE For all patients, muscle samples will be removed from the deltoid muscle by open biopsy under local anaesthesia for all patients. The region containing NMJs will be determined by the small twitch provoked by the tip of the scalpel on the surface of the muscle fascicles. For healthy control subjects, biopsy specimens of deltoid muscle will be obtained during shoulder surgery for joint or bone disease. The presence of NMJs on a longitudinal strip of the biopsy specimen will be confirmed using the classic Koelle method revealing cholinesterase activity (Koelle and Friedenwald ,1949). Each biopsy specimen will be sub-divided into several muscle fragments. For confocal imaging study of the morphology of NMJs, muscle samples will be fixed in 4% paraformaldehyde. For electron microscopy study of NMJ ultrastructure, thin strips of muscle from the sample will be fixed in a mixture of paraformaldehyde 2% and glutaraldehyde 2.5%. Several muscle fragments will be fresh frozen in isopentane for histological, biochemical, and molecular studies.