Brain Derived Neurotrophic Factor (BDNF) levels as a possible predictor of psychopathology in healthy twins at high and low risk for affective disorder

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Brain Derived Neurotrophic Factor (BDNF) levels as a possible predictor of psychopathology in healthy twins at high and low risk for affective disorder. / Vinberg, Maj; Miskowiak, Kamilla; Kessing, Lars Vedel.

In: Psychoneuroendocrinology, Vol. 39, 01.2014, p. 179-83.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Vinberg, M, Miskowiak, K & Kessing, LV 2014, 'Brain Derived Neurotrophic Factor (BDNF) levels as a possible predictor of psychopathology in healthy twins at high and low risk for affective disorder', Psychoneuroendocrinology, vol. 39, pp. 179-83. https://doi.org/10.1016/j.psyneuen.2013.09.007

APA

Vinberg, M., Miskowiak, K., & Kessing, L. V. (2014). Brain Derived Neurotrophic Factor (BDNF) levels as a possible predictor of psychopathology in healthy twins at high and low risk for affective disorder. Psychoneuroendocrinology, 39, 179-83. https://doi.org/10.1016/j.psyneuen.2013.09.007

Vancouver

Vinberg M, Miskowiak K, Kessing LV. Brain Derived Neurotrophic Factor (BDNF) levels as a possible predictor of psychopathology in healthy twins at high and low risk for affective disorder. Psychoneuroendocrinology. 2014 Jan;39:179-83. https://doi.org/10.1016/j.psyneuen.2013.09.007

Author

Vinberg, Maj ; Miskowiak, Kamilla ; Kessing, Lars Vedel. / Brain Derived Neurotrophic Factor (BDNF) levels as a possible predictor of psychopathology in healthy twins at high and low risk for affective disorder. In: Psychoneuroendocrinology. 2014 ; Vol. 39. pp. 179-83.

Bibtex

@article{f2208439e30c4a65add5b58ea9785cc4,
title = "Brain Derived Neurotrophic Factor (BDNF) levels as a possible predictor of psychopathology in healthy twins at high and low risk for affective disorder",
abstract = "Brain Derived Neurotrophic Factor (BDNF) is a potential biomarker of affective disorder. However, longitudinal studies evaluating a potential predictive role of BDNF on subsequent psychopathology are lacking. The aim of this study was to investigate whether BDNF alone or in interaction with the BDNF Val66Met polymorphism predict onset of affective disorder in healthy individuals at heritable risk for affective disorder. In a high-risk study, we assessed whole blood levels of BDNF in 234 healthy monozygotic and dizygotic twins with or without a co-twin history of affective disorder (high and low risk twins, respectively). Participants were followed up longitudinally with questionnaires at 6-month intervals for mean seven years and then reassessed with a personal interview to obtain information about whether they had developed psychiatric illness. At follow-up 36 participants (15.4%) had developed psychiatric disorder. Cox regression analysis revealed that BDNF levels at baseline were not associated with onset of illness in this explorative study. Further, two-way interactions between BDNF levels and the Val66Met polymorphism or between familial risk and the Val66Met polymorphism did not predict illness onset.",
keywords = "Adult, Brain-Derived Neurotrophic Factor, Diseases in Twins, Female, Genetic Predisposition to Disease, Genotype, Humans, Life Change Events, Male, Middle Aged, Mood Disorders, Polymorphism, Single Nucleotide, Risk Factors, Twins, Dizygotic, Twins, Monozygotic",
author = "Maj Vinberg and Kamilla Miskowiak and Kessing, {Lars Vedel}",
note = "Copyright {\textcopyright} 2013 Elsevier Ltd. All rights reserved.",
year = "2014",
month = jan,
doi = "10.1016/j.psyneuen.2013.09.007",
language = "English",
volume = "39",
pages = "179--83",
journal = "Psychoneuroendocrinology",
issn = "0306-4530",
publisher = "Pergamon Press",

}

RIS

TY - JOUR

T1 - Brain Derived Neurotrophic Factor (BDNF) levels as a possible predictor of psychopathology in healthy twins at high and low risk for affective disorder

AU - Vinberg, Maj

AU - Miskowiak, Kamilla

AU - Kessing, Lars Vedel

N1 - Copyright © 2013 Elsevier Ltd. All rights reserved.

PY - 2014/1

Y1 - 2014/1

N2 - Brain Derived Neurotrophic Factor (BDNF) is a potential biomarker of affective disorder. However, longitudinal studies evaluating a potential predictive role of BDNF on subsequent psychopathology are lacking. The aim of this study was to investigate whether BDNF alone or in interaction with the BDNF Val66Met polymorphism predict onset of affective disorder in healthy individuals at heritable risk for affective disorder. In a high-risk study, we assessed whole blood levels of BDNF in 234 healthy monozygotic and dizygotic twins with or without a co-twin history of affective disorder (high and low risk twins, respectively). Participants were followed up longitudinally with questionnaires at 6-month intervals for mean seven years and then reassessed with a personal interview to obtain information about whether they had developed psychiatric illness. At follow-up 36 participants (15.4%) had developed psychiatric disorder. Cox regression analysis revealed that BDNF levels at baseline were not associated with onset of illness in this explorative study. Further, two-way interactions between BDNF levels and the Val66Met polymorphism or between familial risk and the Val66Met polymorphism did not predict illness onset.

AB - Brain Derived Neurotrophic Factor (BDNF) is a potential biomarker of affective disorder. However, longitudinal studies evaluating a potential predictive role of BDNF on subsequent psychopathology are lacking. The aim of this study was to investigate whether BDNF alone or in interaction with the BDNF Val66Met polymorphism predict onset of affective disorder in healthy individuals at heritable risk for affective disorder. In a high-risk study, we assessed whole blood levels of BDNF in 234 healthy monozygotic and dizygotic twins with or without a co-twin history of affective disorder (high and low risk twins, respectively). Participants were followed up longitudinally with questionnaires at 6-month intervals for mean seven years and then reassessed with a personal interview to obtain information about whether they had developed psychiatric illness. At follow-up 36 participants (15.4%) had developed psychiatric disorder. Cox regression analysis revealed that BDNF levels at baseline were not associated with onset of illness in this explorative study. Further, two-way interactions between BDNF levels and the Val66Met polymorphism or between familial risk and the Val66Met polymorphism did not predict illness onset.

KW - Adult

KW - Brain-Derived Neurotrophic Factor

KW - Diseases in Twins

KW - Female

KW - Genetic Predisposition to Disease

KW - Genotype

KW - Humans

KW - Life Change Events

KW - Male

KW - Middle Aged

KW - Mood Disorders

KW - Polymorphism, Single Nucleotide

KW - Risk Factors

KW - Twins, Dizygotic

KW - Twins, Monozygotic

U2 - 10.1016/j.psyneuen.2013.09.007

DO - 10.1016/j.psyneuen.2013.09.007

M3 - Journal article

C2 - 24112874

VL - 39

SP - 179

EP - 183

JO - Psychoneuroendocrinology

JF - Psychoneuroendocrinology

SN - 0306-4530

ER -

ID: 138724869