Reduction in Glutamine/Glutamate Levels in the Cerebral Cortex after Adrenocorticotropic Hormone Therapy in Patients with West Syndrome

• Published in: The Tohoku Journal of Experimental Medicine Vol. 232; no. 4; pp. 277 - 283
• Main Authors: Haginoya, Kazuhiro, Munakata, Mitsutoshi, Sakamoto, Osamu, Iinuma, Kazuie, Kure, Shigeo, Kobayashi, Yasuko, Onuma, Akira, Togashi, Noriko
• Format: Journal Article
• Language: English
• Published: Japan Tohoku University Medical Press 01.04.2014
• Subjects: 1H magnetic resonance spectroscopy; adrenocorticotropic hormone; Adrenocorticotropic Hormone - pharmacology; Adrenocorticotropic Hormone - therapeutic use; Aspartic Acid - analogs & derivatives; Aspartic Acid - metabolism; Choline - metabolism; Cosyntropin - pharmacology; Electroencephalography; Female; Glutamic Acid - metabolism; Glutamine - metabolism; glutamine-glutamate cycle; Humans; Infant; Inositol - metabolism; Magnetic Resonance Spectroscopy; Male; Occipital Lobe - metabolism; Spasms, Infantile - drug therapy; Spasms, Infantile - metabolism; Spasms, Infantile - physiopathology; tetracosactide; West syndrome
• ISSN: 0040-8727; 1349-3329; 1349-3329
• DOI: 10.1620/tjem.232.277

West syndrome (WS), an intractable epileptic encephalopathy of infancy, is refractory to many antiepileptic drugs; however, adrenocorticotropic hormone (ACTH) is an effective treatment for WS. The mechanism behind the efficacy of ACTH is mediated by biochemical processes that remain unknown. We examined the effects of ACTH therapy with tetracosactide (TCS), a synthetic ACTH analogue, on brain metabolism in patients with WS, using 1H magnetic resonance spectroscopy (1H-MRS). In six patients with cryptogenic WS, we performed single-voxel 1H-MRS at the occipital lobe cortex. Measurements were taken prior to TCS treatment, a few days after therapy, and several months after therapy. Data were also compared with subjects having only mild psychomotor delays. The metabolites measured were glutamine plus glutamate (Glx), N-acetylaspartate (NAA), choline (Cho), and myoinositol (mI); each was expressed as a ratio with creatine plus phosphocreatine (total creatine: tCr). The Glx/tCr ratio was significantly reduced after the TCS treatment. The NAA/tCr ratio was also significantly reduced after the treatment compared with the control group, although the change in NAA signal was heterogeneous among patients, correlating with respective outcomes. The Cho/tCr and mI/tCr ratios were not affected by TCS treatment. The reduction in Glx suggests a decrease in the glutamate-glutamine cycle, which plays a pivotal role in synthesizing neurotransmitters such as glutamate and GABA. TCS-induced Glx reduction may induce changes in synaptic signal transduction, thereby accounting for the effect of TCS on WS. The change in NAA indicates altered neuronal activity, which may be correlated with outcome in WS patients.