Matches in SemOpenAlex for { <https://semopenalex.org/work/W2980454845> ?p ?o ?g. }
Showing items 1 to 92 of
92
with 100 items per page.
- W2980454845 abstract "Background More than 50% of patients with major depressive episode (MDE) fail to respond to initial treatment with first line pharmacological therapy. Altered receptor and serotonin transporter function are considered to be associated with mental disorders. Our investigation aimed on the density of the HT1A receptor in mesiotemporal cortex (MTC) and raphe measured by F18-Mefway in patients with MDD. Methods Patients with untreated clinically suspected major depressive episode were recruited from June 2012 to May 2014. 49 patients were included into the study: 36 patients (73%) were identified as responders, whereas 13 (27%) were non-responders. Gender distribution was 26 men (56%) and 23 women (44%). For treatment, only a standard medication of a selective serotonin reuptake inhibitor (SSRI) with escitalopram in a range of 10-20 mg/day was permitted. Responders were defined by improvement of the MADRS>50%. Visually MTC had the highest uptake of F18-Mefway among all brain regions, an asymmetry could not be observed in any patient. An elliptical region was drawn over the amygdala and hippocampus area and a small circular region was drawn over the raphe nuclei. All data were calculated related to (unspecific) cerebellar uptake. Results The quotient of the right MTC was 5.00 [4.33; 5.50] in all patients, in responders 5.00 [4.00; 5.75] and in non-responders 5.00 [4.50; 5.50] (P=0.56). The quotient of the left MTC presented with a median level of 4.50 [4.50; 5.50] in all persons. The responders had 4.50 [4.50; 5.75] which was not statistically significant to the data of the non-responders with 5.00 [4.50; 5.50] at P=0.64. The raphe had a median quotient of 2.50 [2.00; 3.00] in all and the cohort of responders, whereas non-responders had 2.50 [2.00; 2.50] (P=0.61). Also the absolute values of SUV in the three brain regions were not statistically different between the cohorts. Additionally, we did not find any sex-related differences in our patient group. Conclusions Serotonin 1A receptor density can be assessed efficiently by F18-Mefway and PET-CT in patients with MDE. The method can be estimated as a possible tool for clinical and academic investigation, marked tracer uptake can constantly be observed at MTC and the raphe. Anyhow, under conditions of real life in patient care, it is not possible to distinguish patients with a good prognosis who will respond to standard SSRI therapy from non-responders who would benefit from a different therapeutic approach starting earlier." @default.
- W2980454845 created "2019-10-25" @default.
- W2980454845 creator A5036765908 @default.
- W2980454845 creator A5054644896 @default.
- W2980454845 creator A5056147162 @default.
- W2980454845 creator A5060736364 @default.
- W2980454845 creator A5069704332 @default.
- W2980454845 creator A5076304536 @default.
- W2980454845 creator A5081082606 @default.
- W2980454845 date "2020-05-01" @default.
- W2980454845 modified "2023-10-16" @default.
- W2980454845 title "Serotonin 1A receptor density measured by F18-Mefway PET/CT in mesiotemporal cortex and raphe does not discriminate therapeutic response in patients with major depressive episode" @default.
- W2980454845 cites W1531988994 @default.
- W2980454845 cites W1873364006 @default.
- W2980454845 cites W1970506215 @default.
- W2980454845 cites W1985445017 @default.
- W2980454845 cites W1991381469 @default.
- W2980454845 cites W1997548503 @default.
- W2980454845 cites W2007644698 @default.
- W2980454845 cites W2009377980 @default.
- W2980454845 cites W2010664845 @default.
- W2980454845 cites W2011990551 @default.
- W2980454845 cites W2015076008 @default.
- W2980454845 cites W2015142981 @default.
- W2980454845 cites W2015458228 @default.
- W2980454845 cites W2023118385 @default.
- W2980454845 cites W2023225473 @default.
- W2980454845 cites W2035658052 @default.
- W2980454845 cites W2042879184 @default.
- W2980454845 cites W2042966037 @default.
- W2980454845 cites W2050087878 @default.
- W2980454845 cites W2057532104 @default.
- W2980454845 cites W2065912590 @default.
- W2980454845 cites W2069915882 @default.
- W2980454845 cites W2087844899 @default.
- W2980454845 cites W2106531784 @default.
- W2980454845 cites W2129579709 @default.
- W2980454845 cites W2136112701 @default.
- W2980454845 cites W2150034106 @default.
- W2980454845 cites W2158770881 @default.
- W2980454845 cites W2346337222 @default.
- W2980454845 cites W2781680003 @default.
- W2980454845 doi "https://doi.org/10.23736/s1824-4785.18.03039-x" @default.
- W2980454845 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/29916219" @default.
- W2980454845 hasPublicationYear "2020" @default.
- W2980454845 type Work @default.
- W2980454845 sameAs 2980454845 @default.
- W2980454845 citedByCount "1" @default.
- W2980454845 countsByYear W29804548452021 @default.
- W2980454845 crossrefType "journal-article" @default.
- W2980454845 hasAuthorship W2980454845A5036765908 @default.
- W2980454845 hasAuthorship W2980454845A5054644896 @default.
- W2980454845 hasAuthorship W2980454845A5056147162 @default.
- W2980454845 hasAuthorship W2980454845A5060736364 @default.
- W2980454845 hasAuthorship W2980454845A5069704332 @default.
- W2980454845 hasAuthorship W2980454845A5076304536 @default.
- W2980454845 hasAuthorship W2980454845A5081082606 @default.
- W2980454845 hasConcept C126322002 @default.
- W2980454845 hasConcept C15744967 @default.
- W2980454845 hasConcept C169760540 @default.
- W2980454845 hasConcept C170493617 @default.
- W2980454845 hasConcept C2775864247 @default.
- W2980454845 hasConcept C2989005 @default.
- W2980454845 hasConcept C53910766 @default.
- W2980454845 hasConcept C71924100 @default.
- W2980454845 hasConceptScore W2980454845C126322002 @default.
- W2980454845 hasConceptScore W2980454845C15744967 @default.
- W2980454845 hasConceptScore W2980454845C169760540 @default.
- W2980454845 hasConceptScore W2980454845C170493617 @default.
- W2980454845 hasConceptScore W2980454845C2775864247 @default.
- W2980454845 hasConceptScore W2980454845C2989005 @default.
- W2980454845 hasConceptScore W2980454845C53910766 @default.
- W2980454845 hasConceptScore W2980454845C71924100 @default.
- W2980454845 hasIssue "2" @default.
- W2980454845 hasLocation W29804548451 @default.
- W2980454845 hasOpenAccess W2980454845 @default.
- W2980454845 hasPrimaryLocation W29804548451 @default.
- W2980454845 hasRelatedWork W1506602199 @default.
- W2980454845 hasRelatedWork W1558342319 @default.
- W2980454845 hasRelatedWork W1978632621 @default.
- W2980454845 hasRelatedWork W1987096130 @default.
- W2980454845 hasRelatedWork W1988394934 @default.
- W2980454845 hasRelatedWork W2050549307 @default.
- W2980454845 hasRelatedWork W2057003203 @default.
- W2980454845 hasRelatedWork W2064334265 @default.
- W2980454845 hasRelatedWork W2083346731 @default.
- W2980454845 hasRelatedWork W2160769306 @default.
- W2980454845 hasVolume "64" @default.
- W2980454845 isParatext "false" @default.
- W2980454845 isRetracted "false" @default.
- W2980454845 magId "2980454845" @default.
- W2980454845 workType "article" @default.