TY - JOUR
T1 - Increased levels of ascorbic acid in the cerebrospinal fluid of cognitively intact elderly patients with major depression
T2 - A preliminary study
AU - Hashimoto, Kenji
AU - Ishima, Tamaki
AU - Sato, Yasunori
AU - Bruno, Davide
AU - Nierenberg, Jay
AU - Marmar, Charles R.
AU - Zetterberg, Henrik
AU - Blennow, Kaj
AU - Pomara, Nunzio
N1 - Funding Information:
This research was supported by grants from the Strategic Research Program for Brain Sciences from Japan Agency for Medical Research and Development, AMED (to K.H.), and SENSHIN Medical Research Foundation, Japan (to K.H.), the Torsten S?derberg Foundation at the Royal Swedish Academy of Sciences, the Knut and Alice Wallenberg Foundation, the Swedish Research Council and the NIMH (to N.P., R01 MH-080405).
PY - 2017/12/1
Y1 - 2017/12/1
N2 - Major depressive disorder (MDD) in the elderly is a risk factor for dementia, but the precise biological basis remains unknown, hampering the search for novel biomarkers and treatments. In this study, we performed metabolomics analysis of cerebrospinal fluid (CSF) from cognitively intact elderly patients (N = 28) with MDD and age- and gender-matched healthy controls (N = 18). The CSF levels of 177 substances were measured, while 288 substances were below the detection limit. Only ascorbic acid was significantly different, with higher levels in the MDD group at baseline. There were no correlations between CSF ascorbic acid levels and clinical variables in MDD patients at baseline. At the 3-year follow-up, there was no difference of CSF ascorbic acid levels between the two groups. There was a negative correlation between CSF ascorbic acid and CSF amyloid-β42 levels in all subjects. However, there were no correlations between ascorbic acid and other biomarkers (e.g., amyloid-β40, total and phosphorylated tau protein). This preliminary study suggests that abnormalities in the transport and/or release of ascorbic acid might play a role in the pathogenesis of late-life depression.
AB - Major depressive disorder (MDD) in the elderly is a risk factor for dementia, but the precise biological basis remains unknown, hampering the search for novel biomarkers and treatments. In this study, we performed metabolomics analysis of cerebrospinal fluid (CSF) from cognitively intact elderly patients (N = 28) with MDD and age- and gender-matched healthy controls (N = 18). The CSF levels of 177 substances were measured, while 288 substances were below the detection limit. Only ascorbic acid was significantly different, with higher levels in the MDD group at baseline. There were no correlations between CSF ascorbic acid levels and clinical variables in MDD patients at baseline. At the 3-year follow-up, there was no difference of CSF ascorbic acid levels between the two groups. There was a negative correlation between CSF ascorbic acid and CSF amyloid-β42 levels in all subjects. However, there were no correlations between ascorbic acid and other biomarkers (e.g., amyloid-β40, total and phosphorylated tau protein). This preliminary study suggests that abnormalities in the transport and/or release of ascorbic acid might play a role in the pathogenesis of late-life depression.
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U2 - 10.1038/s41598-017-03836-0
DO - 10.1038/s41598-017-03836-0
M3 - Article
C2 - 28615661
AN - SCOPUS:85020510224
VL - 7
JO - Scientific Reports
JF - Scientific Reports
SN - 2045-2322
IS - 1
M1 - 3485
ER -