Psychiatry - Research Publications

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    Effect of High-Intensity Power Training on Cognitive Function in Older Adults With Type 2 Diabetes: Secondary Outcomes of the GREAT2DO Study
    Zhao, RR ; Mavros, Y ; Meiklejohn, J ; Anderberg, KA ; Singh, N ; Kay, S ; Baker, MK ; Wang, Y ; Climstein, M ; O'Sullivan, A ; De Vos, N ; Baune, BT ; Blair, SN ; Simar, D ; Fiatarone Singh, MA ; Le Couteur, D (OXFORD UNIV PRESS INC, 2022-10-06)
    We sought to determine the effects of 12 months of power training on cognition, and whether improvements in body composition, muscle strength, and/or aerobic capacity (VO2peak) were associated with improvements in cognition in older adults with type 2 diabetes (T2D). Participants with T2D were randomized to power training or low-intensity sham exercise control condition, 3 days per week for 12 months. Cognitive outcomes included memory, attention/speed, executive function, and global cognition. Other relevant outcomes included VO2peak, strength, and whole body and regional body composition. One hundred and three adults with T2D (mean age 67.9 years; standard deviation [SD] 5.9; 50.5% women) were enrolled and analyzed. Unexpectedly, there was a nearly significant improvement in global cognition (p = .05) in the sham group relative to power training, although both groups improved over time (p < .01). There were significant interactions between group allocation and body composition or muscle strength in the models predicting cognitive changes. Therefore, after stratifying by group allocation, improvements in immediate memory were associated with increases in relative skeletal muscle mass (r = 0.38, p = .03), reductions in relative body fat (r = -0.40, p = .02), and increases in knee extension strength were directly related to changes in executive function (r = -0.41, p = .02) within the power training group. None of these relationships were present in the sham group (p > .05). Although power training did not significantly improve cognition compared to low-intensity exercise control, improvements in cognitive function in older adults were associated with hypothesized improvements in body composition and strength after power training.
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    Expression of CXCR4 on CD4+ T cells predicts body composition parameters in female adolescents with anorexia nervosa.
    Freff, J ; Bröker, L ; Leite Dantas, R ; Schwarte, K ; Bühlmeier, J ; Kraft, I ; Hinney, A ; Buhlmann, U ; Arolt, V ; Dannlowski, U ; Romer, G ; Baune, BT ; Hebebrand, J ; Föcker, M ; Alferink, J (Frontiers Media SA, 2022)
    Anorexia nervosa (AN) is a severe eating disorder characterized by excessive weight loss and lack of recognition of the seriousness of the current low body weight. Individuals with AN frequently exhibit an enhanced inflammatory state and altered blood levels of cytokines and chemokines. However, the expression of chemokine receptors in AN and the association with body composition parameters and treatment effects are still unknown. In this study, we examined the expression of CCR4, CCR6, CXCR3, and CXCR4 on peripheral blood T cells in female adolescents with AN before (T0, n = 24) and after 6 weeks of multimodal therapy (T1, n = 20). We also investigated their value to predict body mass index (BMI) and fat mass index (FMI) at baseline. Using multi-parameter flow cytometry, we found increased expression of CCR4, CXCR3, and CXCR4, but not CCR6, on CD4+ T cells in AN at T0 when compared to healthy controls (HC, n = 20). At T1, CXCR3 and CXCR4 expression decreased in AN. We found a close link between CCR4, CCR6 and CXCR4 expression and the adolescent mental health status in the study cohort as determined by the Strengths and Difficulties Questionnaire (SDQ). Specifically, CXCR4 expression correlated positively with emotional symptoms and peer relationship problems, as well as with the total sum score of the SDQ. In addition, CXCR4 expression on CD4+ T cells was a significant predictor of BMI and FMI in female adolescents. Our findings that CXCR4 expression on T cells is altered in adolescents with AN and predicts body composition parameters in adolescents suggest an impact of this chemokine receptor in the pathogenesis of AN.
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    Correction to: Biological sex classification with structural MRI data shows increased misclassification in transgender women.
    Flint, C ; Förster, K ; Koser, SA ; Konrad, C ; Zwitserlood, P ; Berger, K ; Hermesdorf, M ; Kircher, T ; Nenadic, I ; Krug, A ; Baune, BT ; Dohm, K ; Redlich, R ; Opel, N ; Arolt, V ; Hahn, T ; Jiang, X ; Dannlowski, U ; Grotegerd, D (Springer Science and Business Media LLC, 2022-01)
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    The Role of Educational Attainment and Brain Morphology in Major Depressive Disorder: Findings From the ENIGMA Major Depressive Disorder Consortium
    Whittle, S ; Rakesh, D ; Schmaal, L ; Veltman, DJ ; Thompson, PM ; Singh, A ; Gonul, AS ; Aleman, A ; Demir, AU ; Krug, A ; Mwangi, B ; Kramer, B ; Baune, BT ; Stein, DJ ; Grotegerd, D ; Pomarol-Clotet, E ; Rodriguez-Cano, E ; Melloni, E ; Benedetti, F ; Stein, F ; Grabe, HJ ; Volzke, H ; Gotlib, IH ; Nenadic, I ; Soares, JC ; Repple, J ; Sim, K ; Brosch, K ; Wittfeld, K ; Berger, K ; Hermesdorf, M ; Portella, MJ ; Sacchet, MD ; Wu, M-J ; Opel, N ; Groenewold, NA ; Gruber, O ; Fuentes-Claramonte, P ; Salvador, R ; Goya-Maldonado, R ; Sarro, S ; Poletti, S ; Meinert, SL ; Kircher, T ; Dannlowski, U ; Pozzi, E (AMER PSYCHOLOGICAL ASSOC, 2022-08)
    Brain structural abnormalities and low educational attainment are consistently associated with major depressive disorder (MDD), yet there has been little research investigating the complex interaction of these factors. Brain structural alterations may represent a vulnerability or differential susceptibility marker, and in the context of low educational attainment, predict MDD. We tested this moderation model in a large multisite sample of 1958 adults with MDD and 2921 controls (aged 18 to 86) from the ENIGMA MDD working group. Using generalized linear mixed models and within-sample split-half replication, we tested whether brain structure interacted with educational attainment to predict MDD status. Analyses revealed that cortical thickness in a number of occipital, parietal, and frontal regions significantly interacted with education to predict MDD. For the majority of regions, models suggested a differential susceptibility effect, whereby thicker cortex was more likely to predict MDD in individuals with low educational attainment, but less likely to predict MDD in individuals with high educational attainment. Findings suggest that greater thickness of brain regions subserving visuomotor and social-cognitive functions confers susceptibility to MDD, dependent on level of educational attainment. Longitudinal work, however, is ultimately needed to establish whether cortical thickness represents a preexisting susceptibility marker. (PsycInfo Database Record (c) 2022 APA, all rights reserved).
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    Networks of inflammation, depression, and cognition in aging males and females.
    Chalmers, RA ; Cervin, M ; Choo, C ; Baune, BT ; Trollor, JN ; Numbers, K ; Sachdev, PS ; Brodaty, H ; Kochan, NA ; Medvedev, ON (Springer Science and Business Media LLC, 2022-10)
    BACKGROUND: Prioritizing the maintenance of healthy cognitive aging and personalizing preventive interventions to enhance their effectiveness is crucial as the global population ages. Systemic inflammation and depression in older people have been associated with decreased levels of cognition but results have been inconsistent. AIMS: To explore the interactive network of inflammation, depression and cognition by sex in older people. METHODS: We used novel network analysis to explore the unique associations between inflammatory biomarkers, depression, cognition, and somatic, genetic, and lifestyle risk factors in an older (aged 70-90 years), non-demented, community-dwelling sample from the longitudinal Sydney Memory and Aging Study (N = 916) at baseline and at a two-year follow-up. RESULTS: The networks of biomarkers, depression, cognition, and relevant covariates were significantly different between males and females. A stable negative link between depression and cognition was found in females only; a stable positive association between biomarker interleukin-6 and depression was found in females only; and a stable positive association between biomarker interleukin-8 and alcohol was found in females only. For both males and females, a stable, positive relationship was found between the presence of APOE-ε4 gene and biomarker C-reactive protein; between education and cognition; and between biomarker interleukin-6 and all other biomarkers. CONCLUSIONS: These findings suggest different psychophysiological mechanisms underlie the interactive network of biomarkers, depression and cognition in males and females that should be considered when designing personalized preventive interventions to maintain cognitively healthy aging.
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    [Vagus nerve stimulation for difficult to treat depression].
    Reif-Leonhard, C ; Reif, A ; Baune, BT ; Kavakbasi, E (Springer Science and Business Media LLC, 2022-09)
    INTRODUCTION: For the past 20 years vagus nerve stimulation (VNS) has been an approved invasive treatment option for treatment-resistant depression (TRD) across Europe. In contrast to more common treatments, such as ECT, knowledge about VNS is low both in the general population and among professionals. METHODS: In this narrative review, we provide a clinically and scientifically sound overview of VNS. Hypotheses on the mechanism of action as well as the current evidence base on efficacy are presented. Perioperative management, adverse event profile and follow-up including dose titration are described. A comparison of international guideline recommendations on VNS is also provided. Furthermore, we formulate criteria that are helpful in the selection of appropriate patients. RESULTS: Electrical impulses are transmitted afferently via the vagus nerve and stimulate a neuromodulatory cerebral network via different pathways. Many studies and case series demonstrated the efficacy of VNS as an adjuvant procedure for TRD. The effect occurs with a latency period of 3-12 months and possibly increases with the duration of VNS. If stimulation recommendations are followed, side effects are tolerable for most patients. CONCLUSION: The use of VNS is an approved, effective and well-tolerated long-term therapy for chronic and treatment-resistant depression. Further sham-controlled studies over a longer observational period are desirable to improve the evidence.
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    Predictive role of atrial fibrillation in cognitive decline: a systematic review and meta-analysis of 2.8 million individuals.
    Koh, YH ; Lew, LZW ; Franke, KB ; Elliott, AD ; Lau, DH ; Thiyagarajah, A ; Linz, D ; Arstall, M ; Tully, PJ ; Baune, BT ; Munawar, DA ; Mahajan, R (Oxford University Press (OUP), 2022-09-01)
    AIMS: To systematic review and meta-analyse the association and mechanistic links between atrial fibrillation (AF) and cognitive impairment. METHODS AND RESULTS: PubMed, EMBASE, and Cochrane Library were searched up to 27 March 2021 and yielded 4534 citations. After exclusions, 61 were analysed; 15 and 6 studies reported on the association of AF and cognitive impairment in the general population and post-stroke cohorts, respectively. Thirty-six studies reported on the neuro-pathological changes in patients with AF; of those, 13 reported on silent cerebral infarction (SCI) and 11 reported on cerebral microbleeds (CMB). Atrial fibrillation was associated with 39% increased risk of cognitive impairment in the general population [n = 15: 2 822 974 patients; hazard ratio = 1.39; 95% confidence interval (CI) 1.25-1.53, I2 = 90.3%; follow-up 3.8-25 years]. In the post-stroke cohort, AF was associated with a 2.70-fold increased risk of cognitive impairment [adjusted odds ratio (OR) 2.70; 95% CI 1.66-3.74, I2 = 0.0%; follow-up 0.25-3.78 years]. Atrial fibrillation was associated with cerebral small vessel disease, such as white matter hyperintensities and CMB (n = 8: 3698 patients; OR = 1.38; 95% CI 1.11-1.73, I2 = 0.0%), SCI (n = 13: 6188 patients; OR = 2.11; 95% CI 1.58-2.64, I2 = 0%), and decreased cerebral perfusion and cerebral volume even in the absence of clinical stroke. CONCLUSION: Atrial fibrillation is associated with increased risk of cognitive impairment. The association with cerebral small vessel disease and cerebral atrophy secondary to cardioembolism and cerebral hypoperfusion may suggest a plausible link in the absence of clinical stroke. PROSPERO CRD42018109185.
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    Corrigendum: Potential genetic overlap between insomnia and sleep symptoms in major depressive disorder: A polygenic risk score analysis.
    Melhuish Beaupre, LM ; Tiwari, AK ; Gonçalves, VF ; Zai, CC ; Marshe, VS ; Lewis, CM ; Martin, NG ; McIntosh, AM ; Adams, MJ ; Baune, BT ; Levinson, DF ; Boomsma, DI ; Penninx, BWJH ; Breen, G ; Hamilton, S ; Awasthi, S ; Ripke, S ; Jones, L ; Jones, I ; Byrne, EM ; Hickie, IB ; Potash, JP ; Shi, J ; Weissman, MM ; Milaneschi, Y ; Shyn, SI ; de Geus, EJC ; Willemsen, G ; Brown, GM ; Kennedy, JL ; Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, (Frontiers Media SA, 2022)
    [This corrects the article DOI: 10.3389/fpsyt.2021.734077.].
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    Transdiagnostic Cognitive-Behavioral Therapy for Depression and Anxiety Disorders in Cardiovascular Disease Patients: Results From the CHAMPS Pilot-Feasibility Trial.
    Tully, PJ ; Turnbull, DA ; Horowitz, JD ; Beltrame, JF ; Baune, BT ; Sauer-Zavala, S ; Baumeister, H ; Bean, CG ; Pinto, RB ; Cosh, S ; Wittert, GA (Frontiers Media SA, 2022)
    OBJECTIVE: The aim of the Cardiovascular Health in Anxiety and Mood Problems Study (CHAMPS) is to pilot the Unified Protocol (UP) for the transdiagnostic treatment of depression and anxiety disorders in patients recently hospitalized for cardiovascular diseases (CVDs) and evaluate the feasibility. METHODS: The present study is a controlled, block randomized pragmatic pilot-feasibility trial incorporating qualitative interview data, comparing UP (n = 9) with enhanced usual care (EUC, n = 10). Eligible trial participants had a recent CVD-cause admission and were above the severity threshold for depression or anxiety denoted by Patient Health Questionnaire (PHQ-9) total scores ≥10 and/or Generalized Anxiety Disorder (GAD-7) total scores ≥7 respectively on two occasions, and met criteria for one or more depression or anxiety disorders determined by structured clinical interview. Study outcomes were analyzed as intention-to-treat using linear mixed models and qualitative interview data were analyzed with content analysis. RESULTS: Quantitative and qualitative measured indicated acceptability of the transdiagnostic CBT intervention for CVD patients with depression or anxiety disorders. Satisfaction with UP was comparable to antidepressant therapy and higher than general physician counseling. However, there were difficulties recruiting participants with current disorders and distress on two occasions. The UP was associated with a reduction in total number of disorders determined by blinded raters. Linear mixed models indicated that a significantly greater reduction in anxiety symptoms was evident in the UP group by comparison to the EUC group (GAD-7, p between groups = 0.011; Overall Anxiety Severity and Impairment Scale, p between groups = 0.013). Results favored the UP group by comparison to EUC for change over 6 months on measures of physical quality of life and harmful alcohol use. There was no difference between the two groups on changes in depression symptoms (PHQ-9), stress, metacognitive worry beliefs, physical activity, or adherence. DISCUSSION: In conclusion, this feasibility trial indicates acceptability of transdiagnostic CBT intervention for CVD patients with depression or anxiety disorders that is tempered by difficulties with recruitment. Larger trials are required to clarify the efficacy of transdiagnostic depression and anxiety disorder CBT in populations with CVDs and depressive or anxiety disorders. CLINICAL TRIAL REGISTRATION: https://www.australianclinicaltrials.gov.au/anzctr/trial/ACTRN12615000555550, identifier: ACTRN12615000555550.
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    Combining schizophrenia and depression polygenic risk scores improves the genetic prediction of lithium response in bipolar disorder patients (vol 12, 278, 2022)
    Schubert, KO ; Thalamuthu, A ; Amare, AT ; Frank, J ; Streit, F ; Adl, M ; Akula, N ; Akiyama, K ; Ardau, R ; Arias, B ; Aubry, J-M ; Backlund, L ; Bhattacharjee, AK ; Bellivier, F ; Benabarre, A ; Bengesser, S ; Biernacka, JM ; Birner, A ; Marie-Claire, C ; Cearns, M ; Cervantes, P ; Chen, H-C ; Chillotti, C ; Cichon, S ; Clark, SR ; Cruceanu, C ; Czerski, PM ; Dalkner, N ; Dayer, A ; Degenhardt, F ; Del Zompo, M ; DePaulo, JR ; Etain, B ; Falkai, P ; Forstner, AJ ; Frisen, L ; Frye, MA ; Fullerton, JM ; Gard, S ; Garnham, JS ; Goes, FS ; Grigoroiu-Serbanescu, M ; Grof, P ; Hashimoto, R ; Hauser, J ; Heilbronner, U ; Herms, S ; Hoffmann, P ; Hou, L ; Hsu, Y-H ; Jamain, S ; Jimenez, E ; Kahn, J-P ; Kassem, L ; Kuo, P-H ; Kato, T ; Kelsoe, J ; Kittel-Schneider, S ; Ferensztajn-Rochowiak, E ; Konig, B ; Kusumi, I ; Laje, G ; Landen, M ; Lavebratt, C ; Leboyer, M ; Leckband, SG ; Maj, M ; Manchia, M ; Martinsson, L ; McCarthy, MJ ; McElroy, S ; Colom, F ; Mitjans, M ; Mondimore, FM ; Monteleone, P ; Nievergelt, CM ; Nothen, MM ; Novak, T ; O'Donovan, C ; Ozaki, N ; Osby, U ; Papiol, S ; Pfennig, A ; Pisanu, C ; Potash, JB ; Reif, A ; Reininghaus, E ; Rouleau, GA ; Rybakowski, JK ; Schalling, M ; Schofield, PR ; Schweizer, BW ; Severino, G ; Shekhtman, T ; Shilling, PD ; Shimoda, K ; Simhandl, C ; Slaney, CM ; Squassina, A ; Stamm, T ; Stopkova, P ; Tekola-Ayele, F ; Tortorella, A ; Turecki, G ; Veeh, J ; Vieta, E ; Witt, SH ; Roberts, G ; Zandi, PP ; Alda, M ; Bauer, M ; McMahon, FJ ; Mitchell, PB ; Schulze, TG ; Rietschel, M ; Baune, BT (SPRINGERNATURE, 2022-07-11)