The effect of atorvastatin on cognition and mood in bipolar disorder and unipolar depression patients: A secondary analysis of a randomized controlled trial
Statins have recently been linked to having effects on cognition and mood in mood disorders, though results are mixed. In this paper, we use data from a recent randomized controlled trial (RCT) to examine the effect of statins on cognition and mood in patients with Bipolar Disorder (BD) and Major De...
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Veröffentlicht in: | Journal of affective disorders 2020-02, Vol.262, p.149-154 |
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creator | Fotso Soh, Jocelyn Almadani, Ahmad Beaulieu, Serge Rajji, Tarek Mulsant, Benoit H. Su, Chien-Lin Renaud, Suzane Mucsi, Istvan Torres-Platas, S. Gabriela Levinson, Andrea Schaffer, Ayal Dols, Annemiek Cervantes, Pablo Low, Nancy Herrmann, Nathan Mantere, Outi Rej, Soham |
description | Statins have recently been linked to having effects on cognition and mood in mood disorders, though results are mixed. In this paper, we use data from a recent randomized controlled trial (RCT) to examine the effect of statins on cognition and mood in patients with Bipolar Disorder (BD) and Major Depressive Disorder (MDD).
This is a secondary analysis of a randomized, double-blind, placebo-controlled clinical trial (n = 60) originally designed to examine the effect of atorvastatin (n = 27) versus placebo (n = 33) for lithium-induced diabetes insipidus in BD and MDD patients who were using lithium. For this analysis, the primary outcome was global cognition Z-score at 12-weeks adjusted for baseline. The secondary cognition outcomes were (1) Screen for Cognitive Impairment in Psychiatry (SCIP), and (2) executive function Z-score. The primary mood outcome (secondary outcome of this analysis) was depression relapse during 12-week follow-up (Mongomery Asberg Depression Rating Scale (MADRS) ≥10). The secondary mood outcomes were (1) relapse rate into a manic episode, and (2) relapse rate into any mood episode.
After 12 weeks follow-up, atorvastatin and placebo groups did not differ in terms of global cognition Z-score (β = −0.009287 (−0.1698,0.1512), p-value = 0.91). Similarly, composite Z-scores for SCIP and executive functions did not differ significantly. Depression relapse during 12-week follow-up was not significantly different between the groups (χ2 (1) = 0.148, p-value = 0.70). Similarly, there was no difference between groups regarding relapse into mania.
In BD and MDD patients with lithium-induced nephrogenic diabetes insipidus randomized to atorvastatin or placebo, we found no significant differences in cognition and mood outcomes at 12-week follow-up. |
doi_str_mv | 10.1016/j.jad.2019.11.013 |
format | Article |
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This is a secondary analysis of a randomized, double-blind, placebo-controlled clinical trial (n = 60) originally designed to examine the effect of atorvastatin (n = 27) versus placebo (n = 33) for lithium-induced diabetes insipidus in BD and MDD patients who were using lithium. For this analysis, the primary outcome was global cognition Z-score at 12-weeks adjusted for baseline. The secondary cognition outcomes were (1) Screen for Cognitive Impairment in Psychiatry (SCIP), and (2) executive function Z-score. The primary mood outcome (secondary outcome of this analysis) was depression relapse during 12-week follow-up (Mongomery Asberg Depression Rating Scale (MADRS) ≥10). The secondary mood outcomes were (1) relapse rate into a manic episode, and (2) relapse rate into any mood episode.
After 12 weeks follow-up, atorvastatin and placebo groups did not differ in terms of global cognition Z-score (β = −0.009287 (−0.1698,0.1512), p-value = 0.91). Similarly, composite Z-scores for SCIP and executive functions did not differ significantly. Depression relapse during 12-week follow-up was not significantly different between the groups (χ2 (1) = 0.148, p-value = 0.70). Similarly, there was no difference between groups regarding relapse into mania.
In BD and MDD patients with lithium-induced nephrogenic diabetes insipidus randomized to atorvastatin or placebo, we found no significant differences in cognition and mood outcomes at 12-week follow-up.</description><identifier>ISSN: 0165-0327</identifier><identifier>EISSN: 1573-2517</identifier><identifier>DOI: 10.1016/j.jad.2019.11.013</identifier><identifier>PMID: 31733459</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Adult ; Affect - drug effects ; Atorvastatin - pharmacology ; Bipolar disorder ; Bipolar Disorder - drug therapy ; Bipolar Disorder - psychology ; Cognition ; Cognition - drug effects ; Depressive Disorder, Major - drug therapy ; Depressive Disorder, Major - psychology ; Double-Blind Method ; Executive Function ; Female ; Humans ; Hydroxymethylglutaryl-CoA Reductase Inhibitors - pharmacology ; Major depressive disorder ; Male ; Middle Aged ; Placebo ; Randomized clinical trial ; Statins ; Treatment Outcome</subject><ispartof>Journal of affective disorders, 2020-02, Vol.262, p.149-154</ispartof><rights>2019 Elsevier B.V.</rights><rights>Copyright © 2019 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c353t-d771930cb3f0c130df193dc219f8bf86147319e5218e91fb88cbdb0143115e83</citedby><cites>FETCH-LOGICAL-c353t-d771930cb3f0c130df193dc219f8bf86147319e5218e91fb88cbdb0143115e83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0165032719320713$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31733459$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fotso Soh, Jocelyn</creatorcontrib><creatorcontrib>Almadani, Ahmad</creatorcontrib><creatorcontrib>Beaulieu, Serge</creatorcontrib><creatorcontrib>Rajji, Tarek</creatorcontrib><creatorcontrib>Mulsant, Benoit H.</creatorcontrib><creatorcontrib>Su, Chien-Lin</creatorcontrib><creatorcontrib>Renaud, Suzane</creatorcontrib><creatorcontrib>Mucsi, Istvan</creatorcontrib><creatorcontrib>Torres-Platas, S. Gabriela</creatorcontrib><creatorcontrib>Levinson, Andrea</creatorcontrib><creatorcontrib>Schaffer, Ayal</creatorcontrib><creatorcontrib>Dols, Annemiek</creatorcontrib><creatorcontrib>Cervantes, Pablo</creatorcontrib><creatorcontrib>Low, Nancy</creatorcontrib><creatorcontrib>Herrmann, Nathan</creatorcontrib><creatorcontrib>Mantere, Outi</creatorcontrib><creatorcontrib>Rej, Soham</creatorcontrib><title>The effect of atorvastatin on cognition and mood in bipolar disorder and unipolar depression patients: A secondary analysis of a randomized controlled trial</title><title>Journal of affective disorders</title><addtitle>J Affect Disord</addtitle><description>Statins have recently been linked to having effects on cognition and mood in mood disorders, though results are mixed. In this paper, we use data from a recent randomized controlled trial (RCT) to examine the effect of statins on cognition and mood in patients with Bipolar Disorder (BD) and Major Depressive Disorder (MDD).
This is a secondary analysis of a randomized, double-blind, placebo-controlled clinical trial (n = 60) originally designed to examine the effect of atorvastatin (n = 27) versus placebo (n = 33) for lithium-induced diabetes insipidus in BD and MDD patients who were using lithium. For this analysis, the primary outcome was global cognition Z-score at 12-weeks adjusted for baseline. The secondary cognition outcomes were (1) Screen for Cognitive Impairment in Psychiatry (SCIP), and (2) executive function Z-score. The primary mood outcome (secondary outcome of this analysis) was depression relapse during 12-week follow-up (Mongomery Asberg Depression Rating Scale (MADRS) ≥10). The secondary mood outcomes were (1) relapse rate into a manic episode, and (2) relapse rate into any mood episode.
After 12 weeks follow-up, atorvastatin and placebo groups did not differ in terms of global cognition Z-score (β = −0.009287 (−0.1698,0.1512), p-value = 0.91). Similarly, composite Z-scores for SCIP and executive functions did not differ significantly. Depression relapse during 12-week follow-up was not significantly different between the groups (χ2 (1) = 0.148, p-value = 0.70). Similarly, there was no difference between groups regarding relapse into mania.
In BD and MDD patients with lithium-induced nephrogenic diabetes insipidus randomized to atorvastatin or placebo, we found no significant differences in cognition and mood outcomes at 12-week follow-up.</description><subject>Adult</subject><subject>Affect - drug effects</subject><subject>Atorvastatin - pharmacology</subject><subject>Bipolar disorder</subject><subject>Bipolar Disorder - drug therapy</subject><subject>Bipolar Disorder - psychology</subject><subject>Cognition</subject><subject>Cognition - drug effects</subject><subject>Depressive Disorder, Major - drug therapy</subject><subject>Depressive Disorder, Major - psychology</subject><subject>Double-Blind Method</subject><subject>Executive Function</subject><subject>Female</subject><subject>Humans</subject><subject>Hydroxymethylglutaryl-CoA Reductase Inhibitors - pharmacology</subject><subject>Major depressive disorder</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Placebo</subject><subject>Randomized clinical trial</subject><subject>Statins</subject><subject>Treatment Outcome</subject><issn>0165-0327</issn><issn>1573-2517</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc9u1DAQxi0EokvhAbggH7kkeOLNOoFTVfFPqsRl75Zjj8GrxA62t1J5lj4ss92WIyeP7d_3jWY-xt6CaEHA7sOhPRjXdgLGFqAVIJ-xDfRKNl0P6jnbENM3Qnbqgr0q5SCE2I1KvGQXEpSU237csPv9L-ToPdrKk-empnxrSjU1RJ4it-lnDDVQZaLjS0qO08cU1jSbzF0oKTvMD5_H-PSKa8ZSTqKVfDDW8pFf8YI2RWfyHdFmviuhPDTkmcRpCX_QUbdYc5pnKmsOZn7NXngzF3zzeF6y_ZfP--tvzc2Pr9-vr24aK3tZG6cUjFLYSXphQQrn6epsB6MfJj_sYKskjNh3MOAIfhoGO7lJwFYC9DjIS_b-bLvm9PuIpeolFIvzbCKmY9GdhJ72DWpHKJxRm1MpGb1ec1hoKA1CnzLRB02Z6FMmGkBTJqR592h_nBZ0_xRPIRDw6QwgzXgbMOtiaW0WXciUi3Yp_Mf-Lw_OnzE</recordid><startdate>20200201</startdate><enddate>20200201</enddate><creator>Fotso Soh, Jocelyn</creator><creator>Almadani, Ahmad</creator><creator>Beaulieu, Serge</creator><creator>Rajji, Tarek</creator><creator>Mulsant, Benoit H.</creator><creator>Su, Chien-Lin</creator><creator>Renaud, Suzane</creator><creator>Mucsi, Istvan</creator><creator>Torres-Platas, S. Gabriela</creator><creator>Levinson, Andrea</creator><creator>Schaffer, Ayal</creator><creator>Dols, Annemiek</creator><creator>Cervantes, Pablo</creator><creator>Low, Nancy</creator><creator>Herrmann, Nathan</creator><creator>Mantere, Outi</creator><creator>Rej, Soham</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20200201</creationdate><title>The effect of atorvastatin on cognition and mood in bipolar disorder and unipolar depression patients: A secondary analysis of a randomized controlled trial</title><author>Fotso Soh, Jocelyn ; Almadani, Ahmad ; Beaulieu, Serge ; Rajji, Tarek ; Mulsant, Benoit H. ; Su, Chien-Lin ; Renaud, Suzane ; Mucsi, Istvan ; Torres-Platas, S. 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Gabriela</creatorcontrib><creatorcontrib>Levinson, Andrea</creatorcontrib><creatorcontrib>Schaffer, Ayal</creatorcontrib><creatorcontrib>Dols, Annemiek</creatorcontrib><creatorcontrib>Cervantes, Pablo</creatorcontrib><creatorcontrib>Low, Nancy</creatorcontrib><creatorcontrib>Herrmann, Nathan</creatorcontrib><creatorcontrib>Mantere, Outi</creatorcontrib><creatorcontrib>Rej, Soham</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of affective disorders</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fotso Soh, Jocelyn</au><au>Almadani, Ahmad</au><au>Beaulieu, Serge</au><au>Rajji, Tarek</au><au>Mulsant, Benoit H.</au><au>Su, Chien-Lin</au><au>Renaud, Suzane</au><au>Mucsi, Istvan</au><au>Torres-Platas, S. Gabriela</au><au>Levinson, Andrea</au><au>Schaffer, Ayal</au><au>Dols, Annemiek</au><au>Cervantes, Pablo</au><au>Low, Nancy</au><au>Herrmann, Nathan</au><au>Mantere, Outi</au><au>Rej, Soham</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The effect of atorvastatin on cognition and mood in bipolar disorder and unipolar depression patients: A secondary analysis of a randomized controlled trial</atitle><jtitle>Journal of affective disorders</jtitle><addtitle>J Affect Disord</addtitle><date>2020-02-01</date><risdate>2020</risdate><volume>262</volume><spage>149</spage><epage>154</epage><pages>149-154</pages><issn>0165-0327</issn><eissn>1573-2517</eissn><abstract>Statins have recently been linked to having effects on cognition and mood in mood disorders, though results are mixed. In this paper, we use data from a recent randomized controlled trial (RCT) to examine the effect of statins on cognition and mood in patients with Bipolar Disorder (BD) and Major Depressive Disorder (MDD).
This is a secondary analysis of a randomized, double-blind, placebo-controlled clinical trial (n = 60) originally designed to examine the effect of atorvastatin (n = 27) versus placebo (n = 33) for lithium-induced diabetes insipidus in BD and MDD patients who were using lithium. For this analysis, the primary outcome was global cognition Z-score at 12-weeks adjusted for baseline. The secondary cognition outcomes were (1) Screen for Cognitive Impairment in Psychiatry (SCIP), and (2) executive function Z-score. The primary mood outcome (secondary outcome of this analysis) was depression relapse during 12-week follow-up (Mongomery Asberg Depression Rating Scale (MADRS) ≥10). The secondary mood outcomes were (1) relapse rate into a manic episode, and (2) relapse rate into any mood episode.
After 12 weeks follow-up, atorvastatin and placebo groups did not differ in terms of global cognition Z-score (β = −0.009287 (−0.1698,0.1512), p-value = 0.91). Similarly, composite Z-scores for SCIP and executive functions did not differ significantly. Depression relapse during 12-week follow-up was not significantly different between the groups (χ2 (1) = 0.148, p-value = 0.70). Similarly, there was no difference between groups regarding relapse into mania.
In BD and MDD patients with lithium-induced nephrogenic diabetes insipidus randomized to atorvastatin or placebo, we found no significant differences in cognition and mood outcomes at 12-week follow-up.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>31733459</pmid><doi>10.1016/j.jad.2019.11.013</doi><tpages>6</tpages></addata></record> |
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subjects | Adult Affect - drug effects Atorvastatin - pharmacology Bipolar disorder Bipolar Disorder - drug therapy Bipolar Disorder - psychology Cognition Cognition - drug effects Depressive Disorder, Major - drug therapy Depressive Disorder, Major - psychology Double-Blind Method Executive Function Female Humans Hydroxymethylglutaryl-CoA Reductase Inhibitors - pharmacology Major depressive disorder Male Middle Aged Placebo Randomized clinical trial Statins Treatment Outcome |
title | The effect of atorvastatin on cognition and mood in bipolar disorder and unipolar depression patients: A secondary analysis of a randomized controlled trial |
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