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dc.contributor.author Serafini G,
dc.contributor.author Pompili M,
dc.contributor.author Innamorati M,
dc.contributor.author Girardi N,
dc.contributor.author Strusi L,
dc.contributor.author Gonda, Xénia
dc.contributor.author Rihmer, Zoltán
dc.date.accessioned 2015-07-01T19:07:45Z
dc.date.available 2015-07-01T19:07:45Z
dc.date.issued 2015
dc.identifier.citation pagination=1-12; journalVolume=6; journalTitle=CNS SPECTRUMS;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/1928
dc.identifier.uri doi:10.1017/S1092852913000825
dc.description.abstract Introduction White matter hyperintensities (WMHs) are one the most common neuroimaging findings in patients with bipolar disorder (BD). It has been suggested that WMHs are associated with impaired insight in schizophrenia and schizoaffective patients; however, the relationship between insight and WMHs in BD type I has not been directly investigated. METHODS: Patients with BD-I (148) were recruited and underwent brain magnetic resonance imaging (MRI). Affective symptoms were assessed using Young Mania Rating Scale (YMRS) and Hamilton Depression Rating Scale (HDRS17); the presence of impaired insight was based on the corresponding items of YMRS and HDRS17. RESULTS: Multiple punctate periventricular WMHs (PWMHs) and deep WMHs (DWMHs) were observed in 49.3% and 39.9% of the cases, respectively. Subjects with lower insight for mania had significantly more PWMHs (54.6% vs 22.2%; p < 0.05) when compared to BD-I patients with higher insight for mania. The presence of PWMHs was independently associated with lower insight for mania: patients who denied illness according to the YMRS were 4 times more likely to have PWMHs (95% CI: 1.21/13.42) than other patients. CONCLUSIONS: Impaired insight in BD-I is associated with periventricular WMHs. The early identification of BD-I subjects with PWMHs and impaired insight may be crucial for clinicians.
dc.relation.ispartof urn:issn:1092-8529
dc.title The impact of periventricular white matter lesions in patients with bipolar disorder type I.
dc.type Journal Article
dc.date.updated 2015-07-01T19:06:41Z
dc.language.rfc3066 en
dc.identifier.mtmt 2575031
dc.identifier.pubmed 24411553
dc.contributor.department SE/GYTK/Gyógyszerhatástani Intézet
dc.contributor.department SE/KSZE/Kútvölgyi Klinikai Tömb Klinikai és Kutatási Mentálhigiénés Osztály
dc.contributor.institution Semmelweis Egyetem


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