Brain-derived neurotrophic factor, impaired glucose metabolism, and bipolar disorder course

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Brain-derived neurotrophic factor, impaired glucose metabolism, and bipolar disorder course. / Mansur, Rodrigo B; Santos, Camila M; Rizzo, Lucas B; Asevedo, Elson; Cunha, Graccielle R; Noto, Mariane N; Pedrini, Mariana; Zeni-Graiff, Maiara; Cordeiro, Quirino; Vinberg, Maj; Kapczinski, Flavio; McIntyre, Roger S; Brietzke, Elisa.

I: Bipolar Disorders (English Edition, Print), Bind 18, Nr. 4, 06.2016, s. 373-378.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Mansur, RB, Santos, CM, Rizzo, LB, Asevedo, E, Cunha, GR, Noto, MN, Pedrini, M, Zeni-Graiff, M, Cordeiro, Q, Vinberg, M, Kapczinski, F, McIntyre, RS & Brietzke, E 2016, 'Brain-derived neurotrophic factor, impaired glucose metabolism, and bipolar disorder course', Bipolar Disorders (English Edition, Print), bind 18, nr. 4, s. 373-378. https://doi.org/10.1111/bdi.12399

APA

Mansur, R. B., Santos, C. M., Rizzo, L. B., Asevedo, E., Cunha, G. R., Noto, M. N., Pedrini, M., Zeni-Graiff, M., Cordeiro, Q., Vinberg, M., Kapczinski, F., McIntyre, R. S., & Brietzke, E. (2016). Brain-derived neurotrophic factor, impaired glucose metabolism, and bipolar disorder course. Bipolar Disorders (English Edition, Print), 18(4), 373-378. https://doi.org/10.1111/bdi.12399

Vancouver

Mansur RB, Santos CM, Rizzo LB, Asevedo E, Cunha GR, Noto MN o.a. Brain-derived neurotrophic factor, impaired glucose metabolism, and bipolar disorder course. Bipolar Disorders (English Edition, Print). 2016 jun.;18(4):373-378. https://doi.org/10.1111/bdi.12399

Author

Mansur, Rodrigo B ; Santos, Camila M ; Rizzo, Lucas B ; Asevedo, Elson ; Cunha, Graccielle R ; Noto, Mariane N ; Pedrini, Mariana ; Zeni-Graiff, Maiara ; Cordeiro, Quirino ; Vinberg, Maj ; Kapczinski, Flavio ; McIntyre, Roger S ; Brietzke, Elisa. / Brain-derived neurotrophic factor, impaired glucose metabolism, and bipolar disorder course. I: Bipolar Disorders (English Edition, Print). 2016 ; Bind 18, Nr. 4. s. 373-378.

Bibtex

@article{30d120faf07841b48650a0c03cc7f057,
title = "Brain-derived neurotrophic factor, impaired glucose metabolism, and bipolar disorder course",
abstract = "OBJECTIVES: The neurotrophin brain-derived neurotrophic factor (BDNF) has been proposed as a potential biomarker in bipolar disorder (BD). However, current evidence is limited and results have been highly heterogeneous. This study aimed to assess the moderating effect of impaired glucose metabolism (IGM) on plasma levels of BDNF in individuals with BD, and on the relationship between BDNF and variables of illness course.METHODS: We measured and compared the plasma levels of BDNF in individuals with BD (n=57) and healthy controls (n=26). IGM was operationalized as pre-diabetes or type 2 diabetes mellitus. Information related to current and past psychiatric/medical history, as well as prescription of pharmacological treatments was also captured.RESULTS: Individuals with BD had lower levels of BDNF, relative to healthy controls, after adjustment for age, gender, current medications, smoking, alcohol use, and IGM (P=.046). There was no effect of IGM (P=.860) and no interaction between BD diagnosis and IGM (P=.893). Peripheral BDNF levels were positively correlated with lifetime depressive episodes (P<.001), psychiatric hospitalizations (P=.001) and suicide attempts (P=.021). IGM moderated the association between BDNF and the number of previous mood episodes (P<.001), wherein there was a positive correlation in euglycemic participants and a negative correlation in individuals with IGM.CONCLUSIONS: BD is independently associated with lower levels of BDNF; IGM may modify the relationship between BDNF and BD course, suggesting an interactive effect of BDNF with metabolic status on illness progression.",
author = "Mansur, {Rodrigo B} and Santos, {Camila M} and Rizzo, {Lucas B} and Elson Asevedo and Cunha, {Graccielle R} and Noto, {Mariane N} and Mariana Pedrini and Maiara Zeni-Graiff and Quirino Cordeiro and Maj Vinberg and Flavio Kapczinski and McIntyre, {Roger S} and Elisa Brietzke",
note = "{\textcopyright} 2016 John Wiley & Sons A/S Published by John Wiley & Sons Ltd.",
year = "2016",
month = jun,
doi = "10.1111/bdi.12399",
language = "English",
volume = "18",
pages = "373--378",
journal = "Bipolar Disorders, Supplement",
issn = "1399-2406",
publisher = "Wiley-Blackwell",
number = "4",

}

RIS

TY - JOUR

T1 - Brain-derived neurotrophic factor, impaired glucose metabolism, and bipolar disorder course

AU - Mansur, Rodrigo B

AU - Santos, Camila M

AU - Rizzo, Lucas B

AU - Asevedo, Elson

AU - Cunha, Graccielle R

AU - Noto, Mariane N

AU - Pedrini, Mariana

AU - Zeni-Graiff, Maiara

AU - Cordeiro, Quirino

AU - Vinberg, Maj

AU - Kapczinski, Flavio

AU - McIntyre, Roger S

AU - Brietzke, Elisa

N1 - © 2016 John Wiley & Sons A/S Published by John Wiley & Sons Ltd.

PY - 2016/6

Y1 - 2016/6

N2 - OBJECTIVES: The neurotrophin brain-derived neurotrophic factor (BDNF) has been proposed as a potential biomarker in bipolar disorder (BD). However, current evidence is limited and results have been highly heterogeneous. This study aimed to assess the moderating effect of impaired glucose metabolism (IGM) on plasma levels of BDNF in individuals with BD, and on the relationship between BDNF and variables of illness course.METHODS: We measured and compared the plasma levels of BDNF in individuals with BD (n=57) and healthy controls (n=26). IGM was operationalized as pre-diabetes or type 2 diabetes mellitus. Information related to current and past psychiatric/medical history, as well as prescription of pharmacological treatments was also captured.RESULTS: Individuals with BD had lower levels of BDNF, relative to healthy controls, after adjustment for age, gender, current medications, smoking, alcohol use, and IGM (P=.046). There was no effect of IGM (P=.860) and no interaction between BD diagnosis and IGM (P=.893). Peripheral BDNF levels were positively correlated with lifetime depressive episodes (P<.001), psychiatric hospitalizations (P=.001) and suicide attempts (P=.021). IGM moderated the association between BDNF and the number of previous mood episodes (P<.001), wherein there was a positive correlation in euglycemic participants and a negative correlation in individuals with IGM.CONCLUSIONS: BD is independently associated with lower levels of BDNF; IGM may modify the relationship between BDNF and BD course, suggesting an interactive effect of BDNF with metabolic status on illness progression.

AB - OBJECTIVES: The neurotrophin brain-derived neurotrophic factor (BDNF) has been proposed as a potential biomarker in bipolar disorder (BD). However, current evidence is limited and results have been highly heterogeneous. This study aimed to assess the moderating effect of impaired glucose metabolism (IGM) on plasma levels of BDNF in individuals with BD, and on the relationship between BDNF and variables of illness course.METHODS: We measured and compared the plasma levels of BDNF in individuals with BD (n=57) and healthy controls (n=26). IGM was operationalized as pre-diabetes or type 2 diabetes mellitus. Information related to current and past psychiatric/medical history, as well as prescription of pharmacological treatments was also captured.RESULTS: Individuals with BD had lower levels of BDNF, relative to healthy controls, after adjustment for age, gender, current medications, smoking, alcohol use, and IGM (P=.046). There was no effect of IGM (P=.860) and no interaction between BD diagnosis and IGM (P=.893). Peripheral BDNF levels were positively correlated with lifetime depressive episodes (P<.001), psychiatric hospitalizations (P=.001) and suicide attempts (P=.021). IGM moderated the association between BDNF and the number of previous mood episodes (P<.001), wherein there was a positive correlation in euglycemic participants and a negative correlation in individuals with IGM.CONCLUSIONS: BD is independently associated with lower levels of BDNF; IGM may modify the relationship between BDNF and BD course, suggesting an interactive effect of BDNF with metabolic status on illness progression.

U2 - 10.1111/bdi.12399

DO - 10.1111/bdi.12399

M3 - Journal article

C2 - 27324989

VL - 18

SP - 373

EP - 378

JO - Bipolar Disorders, Supplement

JF - Bipolar Disorders, Supplement

SN - 1399-2406

IS - 4

ER -

ID: 174175014