Predicting the course of anxiety disorders: The role of biological parameters

Clinical characteristics appear limited in their ability to predict course of anxiety disorders, therefore we explored the predictive value of biological parameters on course of anxiety disorders. 907 persons with an anxiety (panic, social phobia, generalised anxiety) disorder with a baseline and tw...

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Veröffentlicht in:Progress in neuro-psychopharmacology & biological psychiatry 2020-07, Vol.101, p.109924-109924, Article 109924
Hauptverfasser: Bosman, R.C., van Balkom, A.J.L.M., Rhebergen, D., van Hemert, A.M., Schoevers, R.A., Penninx, B.W.J.H., Batelaan, N.M.
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container_title Progress in neuro-psychopharmacology & biological psychiatry
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creator Bosman, R.C.
van Balkom, A.J.L.M.
Rhebergen, D.
van Hemert, A.M.
Schoevers, R.A.
Penninx, B.W.J.H.
Batelaan, N.M.
description Clinical characteristics appear limited in their ability to predict course of anxiety disorders, therefore we explored the predictive value of biological parameters on course of anxiety disorders. 907 persons with an anxiety (panic, social phobia, generalised anxiety) disorder with a baseline and two-year follow-up measure were selected from the Netherlands Study of Depression and Anxiety (NESDA). Previously, three course trajectories were distinguished which vary in terms of symptom severity and chronicity. Baseline clinical parameters like anxiety severity, anxiety duration, and disability were limited in their ability to predict the two-year course. This study explored whether metabolic syndrome, hypothalamic-pituitary-adrenal-axis functioning, inflammation markers, and neuroplasticity were indicators of two-year course and whether these parameters improved the model containing the most predictive clinical parameters only. Baseline diastolic blood pressure of persons with chronic moderate symptoms was significantly higher than of persons with non-chronic mild symptoms (odds ratio [OR] = 1.18, 95% confidence interval [CI95%] 1.01 to 1.38). Baseline high-density lipid cholesterol of persons with severe chronic symptoms was significantly lower than of persons with non-chronic mild symptoms (OR = 0.77, CI95% 0.62 to 0.96). The predictive ability of both parameters was however low with concordance statistics of 0.55 and 0.57 respectively. Addition of biological parameters did not improve the predictive ability of the model containing the clinical parameters. In addition to clinical characteristics, biological parameters did not improve the predictive ability of the model for course trajectory of anxiety disorders. Prediction of course trajectory in anxiety disorders remains difficult and warrants further research. •Anxiety disorders often have a chronic course and relapse or recurrence is common.•Clinical parameters are limited in their ability to predict the course trajectory.•Metabolic syndrome, HPA functioning, inflammation markers and BDNF were studied.•The predictive ability was not improved when these biological parameters were added.•Predicting the course trajectory of anxiety disorders is difficult.
doi_str_mv 10.1016/j.pnpbp.2020.109924
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Previously, three course trajectories were distinguished which vary in terms of symptom severity and chronicity. Baseline clinical parameters like anxiety severity, anxiety duration, and disability were limited in their ability to predict the two-year course. This study explored whether metabolic syndrome, hypothalamic-pituitary-adrenal-axis functioning, inflammation markers, and neuroplasticity were indicators of two-year course and whether these parameters improved the model containing the most predictive clinical parameters only. Baseline diastolic blood pressure of persons with chronic moderate symptoms was significantly higher than of persons with non-chronic mild symptoms (odds ratio [OR] = 1.18, 95% confidence interval [CI95%] 1.01 to 1.38). Baseline high-density lipid cholesterol of persons with severe chronic symptoms was significantly lower than of persons with non-chronic mild symptoms (OR = 0.77, CI95% 0.62 to 0.96). 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Previously, three course trajectories were distinguished which vary in terms of symptom severity and chronicity. Baseline clinical parameters like anxiety severity, anxiety duration, and disability were limited in their ability to predict the two-year course. This study explored whether metabolic syndrome, hypothalamic-pituitary-adrenal-axis functioning, inflammation markers, and neuroplasticity were indicators of two-year course and whether these parameters improved the model containing the most predictive clinical parameters only. Baseline diastolic blood pressure of persons with chronic moderate symptoms was significantly higher than of persons with non-chronic mild symptoms (odds ratio [OR] = 1.18, 95% confidence interval [CI95%] 1.01 to 1.38). Baseline high-density lipid cholesterol of persons with severe chronic symptoms was significantly lower than of persons with non-chronic mild symptoms (OR = 0.77, CI95% 0.62 to 0.96). 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Prediction of course trajectory in anxiety disorders remains difficult and warrants further research. •Anxiety disorders often have a chronic course and relapse or recurrence is common.•Clinical parameters are limited in their ability to predict the course trajectory.•Metabolic syndrome, HPA functioning, inflammation markers and BDNF were studied.•The predictive ability was not improved when these biological parameters were added.•Predicting the course trajectory of anxiety disorders is difficult.</description><subject>Anxiety disorders</subject><subject>BDNF</subject><subject>Course trajectory</subject><subject>HPA-axis</subject><subject>Inflammation markers</subject><subject>Metabolic syndrome</subject><issn>0278-5846</issn><issn>1878-4216</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kEtPwzAMgCMEYmPwC5BQj1w6kjR9IXFAEy8JBIdxjvJwR6a2KUmL2L8nWwdHTracz3b8IXRO8Jxgkl2t513byW5OMd1WypKyAzQlRV7EjJLsEE0xDXlasGyCTrxfY4xJgpNjNEkoyUuS0il6eXOgjepNu4r6D4iUHZyHyFaRaL8N9JtIG2-dBuevo2UAnK13z9LY2q6MEnXUCSca6ANyio4qUXs428cZer-_Wy4e4-fXh6fF7XOsGGZ9TKWQhSzDV0tZpUXCgLBKixxrRXGRS61LAnklWAWiypVUUqalpqxMFCk0y5IZuhznds5-DuB73hivoK5FC3bwnCZ5EY7NGQ5oMqLKWe8dVLxzphFuwwnmW498zXce-dYjHz2Grov9gkE2oP96fsUF4GYEIJz5ZcBxrwy0Ksh0oHqurfl3wQ-wWIXa</recordid><startdate>20200713</startdate><enddate>20200713</enddate><creator>Bosman, R.C.</creator><creator>van Balkom, A.J.L.M.</creator><creator>Rhebergen, D.</creator><creator>van Hemert, A.M.</creator><creator>Schoevers, R.A.</creator><creator>Penninx, B.W.J.H.</creator><creator>Batelaan, N.M.</creator><general>Elsevier Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20200713</creationdate><title>Predicting the course of anxiety disorders: The role of biological parameters</title><author>Bosman, R.C. ; van Balkom, A.J.L.M. ; Rhebergen, D. ; van Hemert, A.M. ; Schoevers, R.A. ; Penninx, B.W.J.H. ; Batelaan, N.M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c404t-2bab8b91879bf5834e14fda70dc2087bdd91e7fa4feaf7cbcbb59d2493c18d463</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Anxiety disorders</topic><topic>BDNF</topic><topic>Course trajectory</topic><topic>HPA-axis</topic><topic>Inflammation markers</topic><topic>Metabolic syndrome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bosman, R.C.</creatorcontrib><creatorcontrib>van Balkom, A.J.L.M.</creatorcontrib><creatorcontrib>Rhebergen, D.</creatorcontrib><creatorcontrib>van Hemert, A.M.</creatorcontrib><creatorcontrib>Schoevers, R.A.</creatorcontrib><creatorcontrib>Penninx, B.W.J.H.</creatorcontrib><creatorcontrib>Batelaan, N.M.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Progress in neuro-psychopharmacology &amp; biological psychiatry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bosman, R.C.</au><au>van Balkom, A.J.L.M.</au><au>Rhebergen, D.</au><au>van Hemert, A.M.</au><au>Schoevers, R.A.</au><au>Penninx, B.W.J.H.</au><au>Batelaan, N.M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Predicting the course of anxiety disorders: The role of biological parameters</atitle><jtitle>Progress in neuro-psychopharmacology &amp; biological psychiatry</jtitle><addtitle>Prog Neuropsychopharmacol Biol Psychiatry</addtitle><date>2020-07-13</date><risdate>2020</risdate><volume>101</volume><spage>109924</spage><epage>109924</epage><pages>109924-109924</pages><artnum>109924</artnum><issn>0278-5846</issn><eissn>1878-4216</eissn><abstract>Clinical characteristics appear limited in their ability to predict course of anxiety disorders, therefore we explored the predictive value of biological parameters on course of anxiety disorders. 907 persons with an anxiety (panic, social phobia, generalised anxiety) disorder with a baseline and two-year follow-up measure were selected from the Netherlands Study of Depression and Anxiety (NESDA). Previously, three course trajectories were distinguished which vary in terms of symptom severity and chronicity. Baseline clinical parameters like anxiety severity, anxiety duration, and disability were limited in their ability to predict the two-year course. This study explored whether metabolic syndrome, hypothalamic-pituitary-adrenal-axis functioning, inflammation markers, and neuroplasticity were indicators of two-year course and whether these parameters improved the model containing the most predictive clinical parameters only. Baseline diastolic blood pressure of persons with chronic moderate symptoms was significantly higher than of persons with non-chronic mild symptoms (odds ratio [OR] = 1.18, 95% confidence interval [CI95%] 1.01 to 1.38). Baseline high-density lipid cholesterol of persons with severe chronic symptoms was significantly lower than of persons with non-chronic mild symptoms (OR = 0.77, CI95% 0.62 to 0.96). 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Prediction of course trajectory in anxiety disorders remains difficult and warrants further research. •Anxiety disorders often have a chronic course and relapse or recurrence is common.•Clinical parameters are limited in their ability to predict the course trajectory.•Metabolic syndrome, HPA functioning, inflammation markers and BDNF were studied.•The predictive ability was not improved when these biological parameters were added.•Predicting the course trajectory of anxiety disorders is difficult.</abstract><cop>England</cop><pub>Elsevier Inc</pub><pmid>32179152</pmid><doi>10.1016/j.pnpbp.2020.109924</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
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subjects Anxiety disorders
BDNF
Course trajectory
HPA-axis
Inflammation markers
Metabolic syndrome
title Predicting the course of anxiety disorders: The role of biological parameters
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