Probing the Association between Cognition, Suicidal Behavior and Tryptophan Metabolism in a Sample of Individuals Living with Bipolar Disorder: A Secondary Analysis
Background and Objectives: Alterations in hot cognition and in the tryptophan metabolism through serotonin (5-HT) and kynurenine (KYN) pathways have been associated with an increased risk of suicidal behavior. Here, we aim at probing the association between Stroop test performances and tryptophan pa...
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Published in | Brain sciences Vol. 13; no. 4; p. 693 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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01.04.2023
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ISSN | 2076-3425 2076-3425 |
DOI | 10.3390/brainsci13040693 |
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Abstract | Background and Objectives: Alterations in hot cognition and in the tryptophan metabolism through serotonin (5-HT) and kynurenine (KYN) pathways have been associated with an increased risk of suicidal behavior. Here, we aim at probing the association between Stroop test performances and tryptophan pathway components in a sample of individuals with bipolar disorder (BD). Materials and Methods: We explored the association between the Emotion Inhibition Subtask (EIS) performances of the Brief Assessment of Cognition for Affective Disorders (BAC-A) and plasmatic levels of 5-hydroxytriptophan (5-HTP), 5-HT, KYN, 3-hydroxykynurenine (3-HK), quinolinic acid (QA), and kynurenic acid (KYNA) among subjects reporting lifetime suicide ideation (LSI) vs. non-LSI and subjects reporting lifetime suicide attempts (LSA) vs. non-LSA. Results: In a sample of 45 subjects with BD, we found a statistically significant different performance for LSA vs. non-LSA in the color naming (CN) and neutral words (NW) EIS subtasks. There was a significant association between CN performances and plasma 5-HTP levels among LSI and LSA subjects but not among non-LSI or non-LSA. Conclusions: In our sample, patients with LSA and LSI presented lower performances on some EIS subtasks compared to non-LSA and non-LSI. Moreover, we found an inverse correlation between plasma 5-HTP concentration and some EIS performances in LSA and LSI but not among non-LSA or non-LSI. This may represent an interesting avenue for future studies probing this complex association. |
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AbstractList | Background and Objectives: Alterations in hot cognition and in the tryptophan metabolism through serotonin (5-HT) and kynurenine (KYN) pathways have been associated with an increased risk of suicidal behavior. Here, we aim at probing the association between Stroop test performances and tryptophan pathway components in a sample of individuals with bipolar disorder (BD). Materials and Methods: We explored the association between the Emotion Inhibition Subtask (EIS) performances of the Brief Assessment of Cognition for Affective Disorders (BAC-A) and plasmatic levels of 5-hydroxytriptophan (5-HTP), 5-HT, KYN, 3-hydroxykynurenine (3-HK), quinolinic acid (QA), and kynurenic acid (KYNA) among subjects reporting lifetime suicide ideation (LSI) vs. non-LSI and subjects reporting lifetime suicide attempts (LSA) vs. non-LSA. Results: In a sample of 45 subjects with BD, we found a statistically significant different performance for LSA vs. non-LSA in the color naming (CN) and neutral words (NW) EIS subtasks. There was a significant association between CN performances and plasma 5-HTP levels among LSI and LSA subjects but not among non-LSI or non-LSA. Conclusions: In our sample, patients with LSA and LSI presented lower performances on some EIS subtasks compared to non-LSA and non-LSI. Moreover, we found an inverse correlation between plasma 5-HTP concentration and some EIS performances in LSA and LSI but not among non-LSA or non-LSI. This may represent an interesting avenue for future studies probing this complex association.Background and Objectives: Alterations in hot cognition and in the tryptophan metabolism through serotonin (5-HT) and kynurenine (KYN) pathways have been associated with an increased risk of suicidal behavior. Here, we aim at probing the association between Stroop test performances and tryptophan pathway components in a sample of individuals with bipolar disorder (BD). Materials and Methods: We explored the association between the Emotion Inhibition Subtask (EIS) performances of the Brief Assessment of Cognition for Affective Disorders (BAC-A) and plasmatic levels of 5-hydroxytriptophan (5-HTP), 5-HT, KYN, 3-hydroxykynurenine (3-HK), quinolinic acid (QA), and kynurenic acid (KYNA) among subjects reporting lifetime suicide ideation (LSI) vs. non-LSI and subjects reporting lifetime suicide attempts (LSA) vs. non-LSA. Results: In a sample of 45 subjects with BD, we found a statistically significant different performance for LSA vs. non-LSA in the color naming (CN) and neutral words (NW) EIS subtasks. There was a significant association between CN performances and plasma 5-HTP levels among LSI and LSA subjects but not among non-LSI or non-LSA. Conclusions: In our sample, patients with LSA and LSI presented lower performances on some EIS subtasks compared to non-LSA and non-LSI. Moreover, we found an inverse correlation between plasma 5-HTP concentration and some EIS performances in LSA and LSI but not among non-LSA or non-LSI. This may represent an interesting avenue for future studies probing this complex association. Background and Objectives: Alterations in hot cognition and in the tryptophan metabolism through serotonin (5-HT) and kynurenine (KYN) pathways have been associated with an increased risk of suicidal behavior. Here, we aim at probing the association between Stroop test performances and tryptophan pathway components in a sample of individuals with bipolar disorder (BD). Materials and Methods: We explored the association between the Emotion Inhibition Subtask (EIS) performances of the Brief Assessment of Cognition for Affective Disorders (BAC-A) and plasmatic levels of 5-hydroxytriptophan (5-HTP), 5-HT, KYN, 3-hydroxykynurenine (3-HK), quinolinic acid (QA), and kynurenic acid (KYNA) among subjects reporting lifetime suicide ideation (LSI) vs. non-LSI and subjects reporting lifetime suicide attempts (LSA) vs. non-LSA. Results: In a sample of 45 subjects with BD, we found a statistically significant different performance for LSA vs. non-LSA in the color naming (CN) and neutral words (NW) EIS subtasks. There was a significant association between CN performances and plasma 5-HTP levels among LSI and LSA subjects but not among non-LSI or non-LSA. Conclusions: In our sample, patients with LSA and LSI presented lower performances on some EIS subtasks compared to non-LSA and non-LSI. Moreover, we found an inverse correlation between plasma 5-HTP concentration and some EIS performances in LSA and LSI but not among non-LSA or non-LSI. This may represent an interesting avenue for future studies probing this complex association. Background and Objectives : Alterations in hot cognition and in the tryptophan metabolism through serotonin (5-HT) and kynurenine (KYN) pathways have been associated with an increased risk of suicidal behavior. Here, we aim at probing the association between Stroop test performances and tryptophan pathway components in a sample of individuals with bipolar disorder (BD). Materials and Methods : We explored the association between the Emotion Inhibition Subtask (EIS) performances of the Brief Assessment of Cognition for Affective Disorders (BAC-A) and plasmatic levels of 5-hydroxytriptophan (5-HTP), 5-HT, KYN, 3-hydroxykynurenine (3-HK), quinolinic acid (QA), and kynurenic acid (KYNA) among subjects reporting lifetime suicide ideation (LSI) vs. non-LSI and subjects reporting lifetime suicide attempts (LSA) vs. non-LSA. Results : In a sample of 45 subjects with BD, we found a statistically significant different performance for LSA vs. non-LSA in the color naming (CN) and neutral words (NW) EIS subtasks. There was a significant association between CN performances and plasma 5-HTP levels among LSI and LSA subjects but not among non-LSI or non-LSA. Conclusions : In our sample, patients with LSA and LSI presented lower performances on some EIS subtasks compared to non-LSA and non-LSI. Moreover, we found an inverse correlation between plasma 5-HTP concentration and some EIS performances in LSA and LSI but not among non-LSA or non-LSI. This may represent an interesting avenue for future studies probing this complex association. : Alterations in hot cognition and in the tryptophan metabolism through serotonin (5-HT) and kynurenine (KYN) pathways have been associated with an increased risk of suicidal behavior. Here, we aim at probing the association between Stroop test performances and tryptophan pathway components in a sample of individuals with bipolar disorder (BD). : We explored the association between the Emotion Inhibition Subtask (EIS) performances of the Brief Assessment of Cognition for Affective Disorders (BAC-A) and plasmatic levels of 5-hydroxytriptophan (5-HTP), 5-HT, KYN, 3-hydroxykynurenine (3-HK), quinolinic acid (QA), and kynurenic acid (KYNA) among subjects reporting lifetime suicide ideation (LSI) vs. non-LSI and subjects reporting lifetime suicide attempts (LSA) vs. non-LSA. : In a sample of 45 subjects with BD, we found a statistically significant different performance for LSA vs. non-LSA in the color naming (CN) and neutral words (NW) EIS subtasks. There was a significant association between CN performances and plasma 5-HTP levels among LSI and LSA subjects but not among non-LSI or non-LSA. : In our sample, patients with LSA and LSI presented lower performances on some EIS subtasks compared to non-LSA and non-LSI. Moreover, we found an inverse correlation between plasma 5-HTP concentration and some EIS performances in LSA and LSI but not among non-LSA or non-LSI. This may represent an interesting avenue for future studies probing this complex association. |
Audience | Academic |
Author | Guiso, Beatrice Pinna, Federica Dall’Acqua, Stefano Bertazzo, Antonella Comai, Stefano Nasini, Sofia Corrias, Carolina Iaselli, Maria Novella Suprani, Federico Squassina, Alessio Garzilli, Mario Somaini, Giulia Pisanu, Claudia Meloni, Anna Pinna, Ilaria Congiu, Donatella Arru, Laura Manchia, Mirko Carpiniello, Bernardo Pulcinelli, Vittoria Paribello, Pasquale Sut, Stefania |
AuthorAffiliation | 2 Unit of Clinical Psychiatry, University Hospital Agency of Cagliari, 09121 Cagliari, Italy 4 Department of Pharmaceutical and Pharmacological Sciences, University of Padova, 35131 Padova, Italy; stefano.dallacqua@unipd.it (S.D.); stefania.sut@unipd.it (S.S.); sofia.nasini@phd.unipd.it (S.N.); antonella.bertazzo@unipd.it (A.B.) 5 Department of Biomedical Sciences, University of Padova, 35131 Padova, Italy 8 Department of Pharmacology, Dalhousie University, Halifax, NS B3H 0A2, Canada 6 San Raffaele Scientific Institute, 20132 Milano, Italy 1 Section of Psychiatry, Department of Medical Sciences and Public Health, University of Cagliari, 09121 Cagliari, Italy; p.paribello@studenti.unica.it (P.P.); m.garzi@gmail.com (M.G.); beatrice.guiso@gmail.com (B.G.); federicosuprani@hotmail.it (F.S.); vittoriapulcinelli@hotmail.com (V.P.); novella.iaselli@gmail.com (M.N.I.); ilaria.pinna1991@gmail.com (I.P.); giulia444@alice.it (G.S.); carol.corrias@gmail.com (C.C.); fedepinna@inwind.it (F.P.); bcarpin |
AuthorAffiliation_xml | – name: 3 Department of Biomedical Science, Section of Neuroscience and Clinical Pharmacology, University of Cagliari, Monserrato, 09042 Cagliari, Italy; squassina@unica.it (A.S.); claudia.pisanu@unica.it (C.P.); anna.meloni@unica.it (A.M.); dcongiu@unica.it (D.C.) – name: 6 San Raffaele Scientific Institute, 20132 Milano, Italy – name: 4 Department of Pharmaceutical and Pharmacological Sciences, University of Padova, 35131 Padova, Italy; stefano.dallacqua@unipd.it (S.D.); stefania.sut@unipd.it (S.S.); sofia.nasini@phd.unipd.it (S.N.); antonella.bertazzo@unipd.it (A.B.) – name: 1 Section of Psychiatry, Department of Medical Sciences and Public Health, University of Cagliari, 09121 Cagliari, Italy; p.paribello@studenti.unica.it (P.P.); m.garzi@gmail.com (M.G.); beatrice.guiso@gmail.com (B.G.); federicosuprani@hotmail.it (F.S.); vittoriapulcinelli@hotmail.com (V.P.); novella.iaselli@gmail.com (M.N.I.); ilaria.pinna1991@gmail.com (I.P.); giulia444@alice.it (G.S.); carol.corrias@gmail.com (C.C.); fedepinna@inwind.it (F.P.); bcarpini@iol.it (B.C.) – name: 7 Department of Psychiatry, McGill University, Montreal, QC H3A 1A1, Canada – name: 5 Department of Biomedical Sciences, University of Padova, 35131 Padova, Italy – name: 2 Unit of Clinical Psychiatry, University Hospital Agency of Cagliari, 09121 Cagliari, Italy – name: 8 Department of Pharmacology, Dalhousie University, Halifax, NS B3H 0A2, Canada |
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CitedBy_id | crossref_primary_10_1016_j_biopsych_2024_09_025 crossref_primary_10_1016_j_jad_2024_01_033 crossref_primary_10_1016_j_jad_2024_08_057 |
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Keywords | affective recognition hot cognition suicide lifetime attempts tryptophan metabolism |
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SubjectTerms | Affective disorders affective recognition Analysis Bipolar disorder Cognition Cognition & reasoning Ethylenediaminetetraacetic acid hot cognition Investigations Kynurenic acid Metabolites Mortality Quinolinic acid Serotonin Statistical analysis Suicidal behavior Suicide suicide lifetime attempts Suicides & suicide attempts Tryptophan tryptophan metabolism |
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Title | Probing the Association between Cognition, Suicidal Behavior and Tryptophan Metabolism in a Sample of Individuals Living with Bipolar Disorder: A Secondary Analysis |
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