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Increased cerebrospinal fluid fibrinogen in major depressive disorder

Major depressive disorder (MDD) presumably includes heterogeneous subgroups with differing pathologies. To obtain a marker reflecting such a subgroup, we analyzed the cerebrospinal fluid (CSF) levels of fibrinogen, which has been reported to be elevated in the plasma of patients with MDD. Three fibr...

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Published in:Scientific reports 2015-06, Vol.5 (1), p.11412-11412, Article 11412
Main Authors: Hattori, Kotaro, Ota, Miho, Sasayama, Daimei, Yoshida, Sumiko, Matsumura, Ryo, Miyakawa, Tomoko, Yokota, Yuuki, Yamaguchi, Shinobu, Noda, Takamasa, Teraishi, Toshiya, Hori, Hiroaki, Higuchi, Teruhiko, Kohsaka, Shinichi, Goto, Yu-ichi, Kunugi, Hiroshi
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Language:English
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Summary:Major depressive disorder (MDD) presumably includes heterogeneous subgroups with differing pathologies. To obtain a marker reflecting such a subgroup, we analyzed the cerebrospinal fluid (CSF) levels of fibrinogen, which has been reported to be elevated in the plasma of patients with MDD. Three fibrinogen-related proteins were measured using aptamer-based analyses and CSF samples of 30 patients with MDD and 30 controls. The numbers of patients with an excessively high level (>99 percentile of the controls) was significantly increased (17 to 23%). Measurement reproducibility of these results was confirmed by an ELISA for fibrinogen (Pearson’s r = 0.77). In an independent sample set from 36 patients and 30 controls, using the ELISA, results were similar (22%). When these two sample sets were combined, the number of patients with a high fibrinogen level was significantly increased (15/66; odds ratio 8.53; 95% confidence interval 1.9–39.1, p = 0.0011). By using diffusion tensor imaging, we found white matter tracts abnormalities in patients with a high fibrinogen level but not those patients with a normal fibrinogen level, compared with controls. Plasma fibrinogen levels were similar among the diagnostic groups. Our results point to a subgroup of MDD represented by increased CSF fibrinogen and white matter tract abnormalities.
ISSN:2045-2322
2045-2322
DOI:10.1038/srep11412