[HTML][HTML] Effects of davunetide on N-acetylaspartate and choline in dorsolateral prefrontal cortex in patients with schizophrenia

LF Jarskog, Z Dong, A Kangarlu, T Colibazzi… - …, 2013 - nature.com
LF Jarskog, Z Dong, A Kangarlu, T Colibazzi, RR Girgis, LS Kegeles, DM Barch
Neuropsychopharmacology, 2013nature.com
Schizophrenia is associated with extensive neurocognitive and behavioral impairments.
Studies indicate that N-acetylaspartate (NAA), a marker of neuronal integrity, and choline, a
marker of cell membrane turnover and white matter integrity, may be altered in
schizophrenia. Davunetide is a neurotrophic peptide that can enhance cognitive function in
animal models of neurodegeneration. Davunetide has recently demonstrated modest
functional improvement in a study of people with schizophrenia. In a subset of these …
Abstract
Schizophrenia is associated with extensive neurocognitive and behavioral impairments. Studies indicate that N-acetylaspartate (NAA), a marker of neuronal integrity, and choline, a marker of cell membrane turnover and white matter integrity, may be altered in schizophrenia. Davunetide is a neurotrophic peptide that can enhance cognitive function in animal models of neurodegeneration. Davunetide has recently demonstrated modest functional improvement in a study of people with schizophrenia. In a subset of these subjects, proton magnetic resonance spectroscopy (1 H-MRS) was conducted to explore the effects of davunetide on change in NAA/creatine (NAA/Cr) and choline/creatine (choline/Cr) over 12 weeks of treatment. Of 63 outpatients with schizophrenia who received randomized davunetide (5 and 30 mg/day) or placebo in the parent clinical trial, 18 successfully completed 1 H-MRS in dorsolateral prefrontal cortex (DLPFC) at baseline and at 12 weeks. Cognition was assessed using the MATRICS Consensus Cognitive Battery (MCCB). NAA/Cr was unchanged for combined high-and low-dose davunetide groups (N= 11). NAA/Cr in the high-dose davunetide group (N= 8) suggested a trend increase of 8.0%(P= 0.072) over placebo (N= 7). Choline/Cr for combined high-and low-dose davunetide groups suggested a 6.4% increase (P= 0.069), while the high-dose group showed a 7.9% increase (P= 0.040) over placebo. Baseline NAA/Cr correlated with the composite MCCB score (R= 0.52, P= 0.033), as did individual cognitive domains of attention/vigilance, verbal learning, and social cognition; however, neither metabolite correlated with functional capacity. In this exploratory study, 12 weeks of adjunctive davunetide appeared to produce modest increases in NAA/Cr and choline/Cr in DLPFC in people with schizophrenia. This is consistent with a potential neuroprotective mechanism for davunetide. The data also support use of MRS as a useful biomarker of baseline cognitive function in schizophrenia. Future clinical and preclinical studies are needed to fully define the mechanism of action and cognitive effects of davunetide in schizophrenia.
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