Establishing the bidirectional relationship between depression and subclinical arteriosclerosis – rationale, design, and characteristics of the BiDirect Study
Depression and cardiovascular diseases due to arteriosclerosis are both frequent and impairing conditions. Depression and (subclinical) arteriosclerosis appear to be related in a bidirectional way, and it is plausible to assume a partly joint causal relationship. However, the biological mechanisms a...
Saved in:
Published in | BMC psychiatry Vol. 14; no. 1; p. 174 |
---|---|
Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
BioMed Central Ltd
13.06.2014
BioMed Central |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | Depression and cardiovascular diseases due to arteriosclerosis are both frequent and impairing conditions. Depression and (subclinical) arteriosclerosis appear to be related in a bidirectional way, and it is plausible to assume a partly joint causal relationship. However, the biological mechanisms and the behavioral pathways that lead from depression to arteriosclerosis and vice versa remain to be exactly determined.
This study protocol describes the rationale and design of the prospective BiDirect Study that aims at investigating the mutual relationship between depression and (subclinical) arteriosclerosis. BiDirect is scheduled to follow-up three distinct cohorts of individuals ((i) patients with acute depression (N = 999), (ii) patients after an acute cardiac event (N = 347), and (iii) reference subjects from the general population (N = 912)). Over the course of 12 years, four personal examinations are planned to be conducted. The core examination program, which will remain identical across follow-ups, comprises a personal interview (e.g. medical diagnoses, health care utilization, lifestyle and risk behavior), a battery of self-administered questionnaires (e.g. depressive symptoms, readiness to change health behavior, perceived health-related quality of life), sensory (e.g. olfaction, pain) and neuropsychological (e.g. memory, executive functions, emotional processing, manual dexterity) assessments, anthropometry, body impedance measurement, a clinical work-up regarding the vascular status (e.g. electrocardiogram, blood pressure, intima media thickness), the taking of blood samples (serum and plasma, DNA), and structural and functional resonance imaging of the brain (e.g. diffusion tensor imaging, resting-state, emotional faces processing). The present report includes BiDirect-Baseline, the first data collection wave.
Due to its prospective character, the integration of three distinct cohorts, the long follow-up time window, the diligent diagnosis of depression taking depression subtypes into account, the consideration of relevant comorbidities and risk factors, the assessment of indicators of (subclinical) arteriosclerosis in different vascular territories, and the structural and functional brain imaging that is performed for a large number of participants, the BiDirect Study represents an innovative approach that combines population-based cohorts with sophisticated clinical work-up methods and that holds the potential to overcome many of the drawbacks characterizing earlier investigations. |
---|---|
AbstractList | Background: Depression and cardiovascular diseases due to arteriosclerosis are both frequent and impairing conditions. Depression and (subclinical) arteriosclerosis appear to be related in a bidirectional way, and it is plausible to assume a partly joint causal relationship. However, the biological mechanisms and the behavioral pathways that lead from depression to arteriosclerosis and vice versa remain to be exactly determined. Methods/design: This study protocol describes the rationale and design of the prospective BiDirect Study that aims at investigating the mutual relationship between depression and (subclinical) arteriosclerosis. BiDirect is scheduled to follow-up three distinct cohorts of individuals ((i) patients with acute depression (N = 999), (ii) patients after an acute cardiac event (N = 347), and (iii) reference subjects from the general population (N = 912)). Over the course of 12 years, four personal examinations are planned to be conducted. The core examination program, which will remain identical across follow-ups, comprises a personal interview (e.g. medical diagnoses, health care utilization, lifestyle and risk behavior), a battery of self-administered questionnaires (e.g. depressive symptoms, readiness to change health behavior, perceived health-related quality of life), sensory (e.g. olfaction, pain) and neuropsychological (e.g. memory, executive functions, emotional processing, manual dexterity) assessments, anthropometry, body impedance measurement, a clinical work-up regarding the vascular status (e.g. electrocardiogram, blood pressure, intima media thickness), the taking of blood samples (serum and plasma, DNA), and structural and functional resonance imaging of the brain (e.g. diffusion tensor imaging, resting-state, emotional faces processing). The present report includes BiDirect-Baseline, the first data collection wave. Discussion: Due to its prospective character, the integration of three distinct cohorts, the long follow-up time window, the diligent diagnosis of depression taking depression subtypes into account, the consideration of relevant comorbidities and risk factors, the assessment of indicators of (subclinical) arteriosclerosis in different vascular territories, and the structural and functional brain imaging that is performed for a large number of participants, the BiDirect Study represents an innovative approach that combines population-based cohorts with sophisticated clinical work-up methods and that holds the potential to overcome many of the drawbacks characterizing earlier investigations. BACKGROUND: Depression and cardiovascular diseases due to arteriosclerosis are both frequent and impairing conditions. Depression and (subclinical) arteriosclerosis appear to be related in a bidirectional way, and it is plausible to assume a partly joint causal relationship. However, the biological mechanisms and the behavioral pathways that lead from depression to arteriosclerosis and vice versa remain to be exactly determined. METHODS/DESIGN: This study protocol describes the rationale and design of the prospective BiDirect Study that aims at investigating the mutual relationship between depression and (subclinical) arteriosclerosis. BiDirect is scheduled to follow-up three distinct cohorts of individuals ((i) patients with acute depression (N = 999), (ii) patients after an acute cardiac event (N = 347), and (iii) reference subjects from the general population (N = 912)). Over the course of 12 years, four personal examinations are planned to be conducted. The core examination program, which will remain identical across follow-ups, comprises a personal interview (e.g. medical diagnoses, health care utilization, lifestyle and risk behavior), a battery of self-administered questionnaires (e.g. depressive symptoms, readiness to change health behavior, perceived health-related quality of life), sensory (e.g. olfaction, pain) and neuropsychological (e.g. memory, executive functions, emotional processing, manual dexterity) assessments, anthropometry, body impedance measurement, a clinical work-up regarding the vascular status (e.g. electrocardiogram, blood pressure, intima media thickness), the taking of blood samples (serum and plasma, DNA), and structural and functional resonance imaging of the brain (e.g. diffusion tensor imaging, resting-state, emotional faces processing). The present report includes BiDirect-Baseline, the first data collection wave. DISCUSSION: Due to its prospective character, the integration of three distinct cohorts, the long follow-up time window, the diligent diagnosis of depression taking depression subtypes into account, the consideration of relevant comorbidities and risk factors, the assessment of indicators of (subclinical) arteriosclerosis in different vascular territories, and the structural and functional brain imaging that is performed for a large number of participants, the BiDirect Study represents an innovative approach that combines population-based cohorts with sophisticated clinical work-up methods and that holds the potential to overcome many of the drawbacks characterizing earlier investigations. Depression and cardiovascular diseases due to arteriosclerosis are both frequent and impairing conditions. Depression and (subclinical) arteriosclerosis appear to be related in a bidirectional way, and it is plausible to assume a partly joint causal relationship. However, the biological mechanisms and the behavioral pathways that lead from depression to arteriosclerosis and vice versa remain to be exactly determined.BACKGROUNDDepression and cardiovascular diseases due to arteriosclerosis are both frequent and impairing conditions. Depression and (subclinical) arteriosclerosis appear to be related in a bidirectional way, and it is plausible to assume a partly joint causal relationship. However, the biological mechanisms and the behavioral pathways that lead from depression to arteriosclerosis and vice versa remain to be exactly determined.This study protocol describes the rationale and design of the prospective BiDirect Study that aims at investigating the mutual relationship between depression and (subclinical) arteriosclerosis. BiDirect is scheduled to follow-up three distinct cohorts of individuals ((i) patients with acute depression (N = 999), (ii) patients after an acute cardiac event (N = 347), and (iii) reference subjects from the general population (N = 912)). Over the course of 12 years, four personal examinations are planned to be conducted. The core examination program, which will remain identical across follow-ups, comprises a personal interview (e.g. medical diagnoses, health care utilization, lifestyle and risk behavior), a battery of self-administered questionnaires (e.g. depressive symptoms, readiness to change health behavior, perceived health-related quality of life), sensory (e.g. olfaction, pain) and neuropsychological (e.g. memory, executive functions, emotional processing, manual dexterity) assessments, anthropometry, body impedance measurement, a clinical work-up regarding the vascular status (e.g. electrocardiogram, blood pressure, intima media thickness), the taking of blood samples (serum and plasma, DNA), and structural and functional resonance imaging of the brain (e.g. diffusion tensor imaging, resting-state, emotional faces processing). The present report includes BiDirect-Baseline, the first data collection wave.METHODS/DESIGNThis study protocol describes the rationale and design of the prospective BiDirect Study that aims at investigating the mutual relationship between depression and (subclinical) arteriosclerosis. BiDirect is scheduled to follow-up three distinct cohorts of individuals ((i) patients with acute depression (N = 999), (ii) patients after an acute cardiac event (N = 347), and (iii) reference subjects from the general population (N = 912)). Over the course of 12 years, four personal examinations are planned to be conducted. The core examination program, which will remain identical across follow-ups, comprises a personal interview (e.g. medical diagnoses, health care utilization, lifestyle and risk behavior), a battery of self-administered questionnaires (e.g. depressive symptoms, readiness to change health behavior, perceived health-related quality of life), sensory (e.g. olfaction, pain) and neuropsychological (e.g. memory, executive functions, emotional processing, manual dexterity) assessments, anthropometry, body impedance measurement, a clinical work-up regarding the vascular status (e.g. electrocardiogram, blood pressure, intima media thickness), the taking of blood samples (serum and plasma, DNA), and structural and functional resonance imaging of the brain (e.g. diffusion tensor imaging, resting-state, emotional faces processing). The present report includes BiDirect-Baseline, the first data collection wave.Due to its prospective character, the integration of three distinct cohorts, the long follow-up time window, the diligent diagnosis of depression taking depression subtypes into account, the consideration of relevant comorbidities and risk factors, the assessment of indicators of (subclinical) arteriosclerosis in different vascular territories, and the structural and functional brain imaging that is performed for a large number of participants, the BiDirect Study represents an innovative approach that combines population-based cohorts with sophisticated clinical work-up methods and that holds the potential to overcome many of the drawbacks characterizing earlier investigations.DISCUSSIONDue to its prospective character, the integration of three distinct cohorts, the long follow-up time window, the diligent diagnosis of depression taking depression subtypes into account, the consideration of relevant comorbidities and risk factors, the assessment of indicators of (subclinical) arteriosclerosis in different vascular territories, and the structural and functional brain imaging that is performed for a large number of participants, the BiDirect Study represents an innovative approach that combines population-based cohorts with sophisticated clinical work-up methods and that holds the potential to overcome many of the drawbacks characterizing earlier investigations. Doc number: 174 Abstract Background: Depression and cardiovascular diseases due to arteriosclerosis are both frequent and impairing conditions. Depression and (subclinical) arteriosclerosis appear to be related in a bidirectional way, and it is plausible to assume a partly joint causal relationship. However, the biological mechanisms and the behavioral pathways that lead from depression to arteriosclerosis and vice versa remain to be exactly determined. Methods/design: This study protocol describes the rationale and design of the prospective BiDirect Study that aims at investigating the mutual relationship between depression and (subclinical) arteriosclerosis. BiDirect is scheduled to follow-up three distinct cohorts of individuals ((i) patients with acute depression (N = 999), (ii) patients after an acute cardiac event (N = 347), and (iii) reference subjects from the general population (N = 912)). Over the course of 12 years, four personal examinations are planned to be conducted. The core examination program, which will remain identical across follow-ups, comprises a personal interview (e.g. medical diagnoses, health care utilization, lifestyle and risk behavior), a battery of self-administered questionnaires (e.g. depressive symptoms, readiness to change health behavior, perceived health-related quality of life), sensory (e.g. olfaction, pain) and neuropsychological (e.g. memory, executive functions, emotional processing, manual dexterity) assessments, anthropometry, body impedance measurement, a clinical work-up regarding the vascular status (e.g. electrocardiogram, blood pressure, intima media thickness), the taking of blood samples (serum and plasma, DNA), and structural and functional resonance imaging of the brain (e.g. diffusion tensor imaging, resting-state, emotional faces processing). The present report includes BiDirect-Baseline, the first data collection wave. Discussion: Due to its prospective character, the integration of three distinct cohorts, the long follow-up time window, the diligent diagnosis of depression taking depression subtypes into account, the consideration of relevant comorbidities and risk factors, the assessment of indicators of (subclinical) arteriosclerosis in different vascular territories, and the structural and functional brain imaging that is performed for a large number of participants, the BiDirect Study represents an innovative approach that combines population-based cohorts with sophisticated clinical work-up methods and that holds the potential to overcome many of the drawbacks characterizing earlier investigations. Depression and cardiovascular diseases due to arteriosclerosis are both frequent and impairing conditions. Depression and (subclinical) arteriosclerosis appear to be related in a bidirectional way, and it is plausible to assume a partly joint causal relationship. However, the biological mechanisms and the behavioral pathways that lead from depression to arteriosclerosis and vice versa remain to be exactly determined. This study protocol describes the rationale and design of the prospective BiDirect Study that aims at investigating the mutual relationship between depression and (subclinical) arteriosclerosis. BiDirect is scheduled to follow-up three distinct cohorts of individuals ((i) patients with acute depression (N = 999), (ii) patients after an acute cardiac event (N = 347), and (iii) reference subjects from the general population (N = 912)). Over the course of 12 years, four personal examinations are planned to be conducted. The core examination program, which will remain identical across follow-ups, comprises a personal interview (e.g. medical diagnoses, health care utilization, lifestyle and risk behavior), a battery of self-administered questionnaires (e.g. depressive symptoms, readiness to change health behavior, perceived health-related quality of life), sensory (e.g. olfaction, pain) and neuropsychological (e.g. memory, executive functions, emotional processing, manual dexterity) assessments, anthropometry, body impedance measurement, a clinical work-up regarding the vascular status (e.g. electrocardiogram, blood pressure, intima media thickness), the taking of blood samples (serum and plasma, DNA), and structural and functional resonance imaging of the brain (e.g. diffusion tensor imaging, resting-state, emotional faces processing). The present report includes BiDirect-Baseline, the first data collection wave. Due to its prospective character, the integration of three distinct cohorts, the long follow-up time window, the diligent diagnosis of depression taking depression subtypes into account, the consideration of relevant comorbidities and risk factors, the assessment of indicators of (subclinical) arteriosclerosis in different vascular territories, and the structural and functional brain imaging that is performed for a large number of participants, the BiDirect Study represents an innovative approach that combines population-based cohorts with sophisticated clinical work-up methods and that holds the potential to overcome many of the drawbacks characterizing earlier investigations. Background Depression and cardiovascular diseases due to arteriosclerosis are both frequent and impairing conditions. Depression and (subclinical) arteriosclerosis appear to be related in a bidirectional way, and it is plausible to assume a partly joint causal relationship. However, the biological mechanisms and the behavioral pathways that lead from depression to arteriosclerosis and vice versa remain to be exactly determined. Methods/design This study protocol describes the rationale and design of the prospective BiDirect Study that aims at investigating the mutual relationship between depression and (subclinical) arteriosclerosis. BiDirect is scheduled to follow-up three distinct cohorts of individuals ((i) patients with acute depression (N = 999), (ii) patients after an acute cardiac event (N = 347), and (iii) reference subjects from the general population (N = 912)). Over the course of 12 years, four personal examinations are planned to be conducted. The core examination program, which will remain identical across follow-ups, comprises a personal interview (e.g. medical diagnoses, health care utilization, lifestyle and risk behavior), a battery of self-administered questionnaires (e.g. depressive symptoms, readiness to change health behavior, perceived health-related quality of life), sensory (e.g. olfaction, pain) and neuropsychological (e.g. memory, executive functions, emotional processing, manual dexterity) assessments, anthropometry, body impedance measurement, a clinical work-up regarding the vascular status (e.g. electrocardiogram, blood pressure, intima media thickness), the taking of blood samples (serum and plasma, DNA), and structural and functional resonance imaging of the brain (e.g. diffusion tensor imaging, resting-state, emotional faces processing). The present report includes BiDirect-Baseline, the first data collection wave. Discussion Due to its prospective character, the integration of three distinct cohorts, the long follow-up time window, the diligent diagnosis of depression taking depression subtypes into account, the consideration of relevant comorbidities and risk factors, the assessment of indicators of (subclinical) arteriosclerosis in different vascular territories, and the structural and functional brain imaging that is performed for a large number of participants, the BiDirect Study represents an innovative approach that combines population-based cohorts with sophisticated clinical work-up methods and that holds the potential to overcome many of the drawbacks characterizing earlier investigations. Keywords: Depression, Depression subtypes, Arteriosclerosis, Cardiovascular, Cerebrovascular, (f)MRI, White matter hyperintensities, Prospective cohort study, Bidirectional Depression and cardiovascular diseases due to arteriosclerosis are both frequent and impairing conditions. Depression and (subclinical) arteriosclerosis appear to be related in a bidirectional way, and it is plausible to assume a partly joint causal relationship. However, the biological mechanisms and the behavioral pathways that lead from depression to arteriosclerosis and vice versa remain to be exactly determined. This study protocol describes the rationale and design of the prospective BiDirect Study that aims at investigating the mutual relationship between depression and (subclinical) arteriosclerosis. BiDirect is scheduled to follow-up three distinct cohorts of individuals ((i) patients with acute depression (N = 999), (ii) patients after an acute cardiac event (N = 347), and (iii) reference subjects from the general population (N = 912)). Over the course of 12 years, four personal examinations are planned to be conducted. The core examination program, which will remain identical across follow-ups, comprises a personal interview (e.g. medical diagnoses, health care utilization, lifestyle and risk behavior), a battery of self-administered questionnaires (e.g. depressive symptoms, readiness to change health behavior, perceived health-related quality of life), sensory (e.g. olfaction, pain) and neuropsychological (e.g. memory, executive functions, emotional processing, manual dexterity) assessments, anthropometry, body impedance measurement, a clinical work-up regarding the vascular status (e.g. electrocardiogram, blood pressure, intima media thickness), the taking of blood samples (serum and plasma, DNA), and structural and functional resonance imaging of the brain (e.g. diffusion tensor imaging, resting-state, emotional faces processing). The present report includes BiDirect-Baseline, the first data collection wave. Due to its prospective character, the integration of three distinct cohorts, the long follow-up time window, the diligent diagnosis of depression taking depression subtypes into account, the consideration of relevant comorbidities and risk factors, the assessment of indicators of (subclinical) arteriosclerosis in different vascular territories, and the structural and functional brain imaging that is performed for a large number of participants, the BiDirect Study represents an innovative approach that combines population-based cohorts with sophisticated clinical work-up methods and that holds the potential to overcome many of the drawbacks characterizing earlier investigations. |
ArticleNumber | 174 |
Audience | Academic |
Author | Nagel, Maren Hense, Hans-Werner Baune, Bernhard T Wellmann, Jürgen Wersching, Heike Teismann, Henning Arolt, Volker Heindel, Walter Berger, Klaus |
AuthorAffiliation | 3 Department for Clinical Radiology, University of Münster, Münster, Germany 4 Discipline of Psychiatry, University of Adelaide, Adelaide, Australia 1 Institute of Epidemiology and Social Medicine, University of Münster, Münster, Germany 2 Department for Psychiatry and Psychotherapy, University of Münster, Münster, Germany |
AuthorAffiliation_xml | – name: 1 Institute of Epidemiology and Social Medicine, University of Münster, Münster, Germany – name: 3 Department for Clinical Radiology, University of Münster, Münster, Germany – name: 4 Discipline of Psychiatry, University of Adelaide, Adelaide, Australia – name: 2 Department for Psychiatry and Psychotherapy, University of Münster, Münster, Germany |
Author_xml | – sequence: 1 givenname: Henning surname: Teismann fullname: Teismann, Henning – sequence: 2 givenname: Heike surname: Wersching fullname: Wersching, Heike – sequence: 3 givenname: Maren surname: Nagel fullname: Nagel, Maren – sequence: 4 givenname: Volker surname: Arolt fullname: Arolt, Volker – sequence: 5 givenname: Walter surname: Heindel fullname: Heindel, Walter – sequence: 6 givenname: Bernhard T surname: Baune fullname: Baune, Bernhard T – sequence: 7 givenname: Jürgen surname: Wellmann fullname: Wellmann, Jürgen – sequence: 8 givenname: Hans-Werner surname: Hense fullname: Hense, Hans-Werner – sequence: 9 givenname: Klaus surname: Berger fullname: Berger, Klaus |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/24924233$$D View this record in MEDLINE/PubMed |
BookMark | eNqNksluFDEQhlsoiCxw54QsceGQDnbbvV2QkiEsUiQOgMTN8lKecdRjD7YblBvvwAvwbDwJ7pkwZKJEQn3oUtVXv0v112Gx57yDonhK8AkhXfOSsJaUFWNfSsJK0rIHxcE2tXcj3i8OY7zEmLRdTR4V-xXrK1ZRelD8Oo9JyMHGhXVzlBaApNU2gErWOzGgAIOYwlxfIQnpO4BDGlYBYsxpJJxGcZRqsM6qzIuQIFgf1QDBRxvR7x8_URAbNTjOrdHO3fG6Ty1EEGriY7IqIm_WA5zZ1-sB0Mc06qvHxUMjhghPrv9Hxec3559m78qLD2_fz04vSll3LJWV7mXLWN9I3WCDa9FJISkQYWSruoqa2piuwpXWLelVbTCArmpGdFMDmVZxVLza6K5GuQStwKUgBr4KdinCFffC8t2Ksws-9984w01Ne5IFZhsBaf09ArsV5Zd8cohPDuWIZwOzyovrMYL_OkJMfGmjgmEQDvwYOakZw4Titv8PlPYtbjvaZvT5LfTSjyE7sqEqTCll_6h5topbZ3yeU02i_DRT9cRNz57cQeVPw9KqfJ_G5vxOw7Obm91u5O8RZgBvAJVPJgYwW4RgPt35XWtqbrUom9ZXloexw_2NfwAlGgVF |
CitedBy_id | crossref_primary_10_1002_hbm_23097 crossref_primary_10_3390_jcm10173937 crossref_primary_10_1186_s40359_020_00485_3 crossref_primary_10_1007_s00330_016_4303_9 crossref_primary_10_1016_j_jad_2016_06_022 crossref_primary_10_3174_ajnr_A5847 crossref_primary_10_1186_s12888_020_02651_8 crossref_primary_10_1080_1028415X_2020_1843892 crossref_primary_10_1038_mp_2017_51 crossref_primary_10_1007_s00702_016_1673_8 crossref_primary_10_1186_s41747_023_00415_z crossref_primary_10_1007_s00127_022_02328_5 crossref_primary_10_1016_j_jad_2017_06_055 crossref_primary_10_1016_j_jneumeth_2015_01_028 crossref_primary_10_3233_JAD_170224 crossref_primary_10_1038_s41380_021_01379_5 crossref_primary_10_1038_s41598_022_20398_y crossref_primary_10_1093_sleep_zsaa209 crossref_primary_10_1038_s41380_024_02688_1 crossref_primary_10_3389_fnagi_2022_810296 crossref_primary_10_1016_j_jpsychores_2021_110513 crossref_primary_10_1016_j_sleep_2015_05_023 crossref_primary_10_1038_s41398_021_01317_7 crossref_primary_10_3389_fpsyt_2020_00412 crossref_primary_10_1126_sciadv_abg9471 crossref_primary_10_3389_fneur_2018_00355 crossref_primary_10_3389_fneur_2022_894119 crossref_primary_10_3389_fnagi_2022_804842 crossref_primary_10_1038_s41593_018_0326_7 crossref_primary_10_1016_j_ebiom_2024_105007 crossref_primary_10_1097_j_pain_0000000000001219 crossref_primary_10_1186_s12888_015_0426_9 crossref_primary_10_1007_s11357_023_00846_x crossref_primary_10_1016_j_jpsychores_2023_111386 crossref_primary_10_1007_s00415_022_11547_4 crossref_primary_10_1016_j_nicl_2017_01_013 crossref_primary_10_1007_s12529_022_10061_1 crossref_primary_10_1016_j_jpsychores_2020_110170 crossref_primary_10_1093_sleep_zsac263 crossref_primary_10_3389_fneur_2023_1145737 crossref_primary_10_1038_s41386_020_0666_3 crossref_primary_10_1016_j_biopsych_2020_04_027 crossref_primary_10_1016_j_psychres_2016_08_035 crossref_primary_10_1093_sleep_zsy237 crossref_primary_10_1007_s00210_019_01627_0 crossref_primary_10_1016_j_jpain_2016_01_474 crossref_primary_10_3389_fnagi_2021_720636 crossref_primary_10_3389_fneur_2022_965031 crossref_primary_10_2174_1745017902016010192 crossref_primary_10_3389_fpsyt_2025_1504123 crossref_primary_10_1080_15622975_2022_2129445 crossref_primary_10_1016_j_sleep_2017_04_010 crossref_primary_10_1016_j_nutres_2018_03_004 crossref_primary_10_1038_s41597_023_02583_4 crossref_primary_10_1016_j_biopsych_2020_07_015 |
Cites_doi | 10.1136/hrt.2010.209767 10.1016/j.genhosppsych.2012.05.013 10.1016/j.pain.2012.02.025 10.3109/07853890109002087 10.1016/S0079-6123(06)56008-X 10.1007/s00103-012-1492-5 10.1007/s00103-012-1491-6 10.2466/PMS.8.7.271-276 10.3174/ajnr.A3713 10.1016/B978-012373960-5.00335-X 10.1097/01.psy.0000162257.19266.fc 10.1016/0165-1781(89)90047-4 10.1017/S1461145708008973 10.1016/j.pcad.2013.03.010 10.1161/01.CIR.93.11.1976 10.1016/j.jad.2011.05.025 10.1093/eurheartj/ehl338 10.1093/eurheartj/eht462 10.1037/h0061266 10.1016/0165-1781(86)90060-0 10.1016/j.neurobiolaging.2006.06.010 10.1111/j.1468-2982.2008.01699.x 10.1177/2047487312467874 10.1038/nature10146 10.1038/tp.2012.18 10.1016/j.jacc.2012.09.058 10.1016/S0006-3223(03)00111-2 10.1177/014662167700100306 10.1136/jnnp.23.1.56 10.1136/jnnp.2007.124651 10.1055/s-0031-1298984 10.1016/j.neurobiolaging.2007.08.023 10.1111/j.2044-8341.1959.tb00467.x 10.1136/bmj.c3666 10.4278/0890-1171-12.1.38 10.1016/j.jacc.2012.11.029 10.1097/01.hjr.0000118174.70522.20 |
ContentType | Journal Article |
Copyright | COPYRIGHT 2014 BioMed Central Ltd. 2014 Teismann et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. Copyright © 2014 Teismann et al.; licensee BioMed Central Ltd. 2014 Teismann et al.; licensee BioMed Central Ltd. |
Copyright_xml | – notice: COPYRIGHT 2014 BioMed Central Ltd. – notice: 2014 Teismann et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. – notice: Copyright © 2014 Teismann et al.; licensee BioMed Central Ltd. 2014 Teismann et al.; licensee BioMed Central Ltd. |
DBID | AAYXX CITATION CGR CUY CVF ECM EIF NPM 3V. 7TK 7X7 7XB 88E 88G 8FI 8FJ 8FK ABUWG AFKRA AZQEC BENPR CCPQU DWQXO FYUFA GHDGH GNUQQ K9. M0S M1P M2M PHGZM PHGZT PIMPY PJZUB PKEHL PPXIY PQEST PQQKQ PQUKI PRINS PSYQQ Q9U 7X8 5PM |
DOI | 10.1186/1471-244X-14-174 |
DatabaseName | CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed ProQuest Central (Corporate) Neurosciences Abstracts ProQuest Health & Medical Collection ProQuest Central (purchase pre-March 2016) Medical Database (Alumni Edition) Psychology Database (Alumni) Hospital Premium Collection Hospital Premium Collection (Alumni Edition) ProQuest Central (Alumni) (purchase pre-March 2016) ProQuest Central (Alumni) ProQuest Central UK/Ireland ProQuest Central Essentials Local Electronic Collection Information ProQuest Central ProQuest One Community College ProQuest Central Korea Health Research Premium Collection Health Research Premium Collection (Alumni) ProQuest Central Student ProQuest Health & Medical Complete (Alumni) ProQuest Health & Medical Collection Medical Database Psychology Database ProQuest Central Premium ProQuest One Academic Publicly Available Content Database ProQuest Health & Medical Research Collection ProQuest One Academic Middle East (New) ProQuest One Health & Nursing ProQuest One Academic Eastern Edition (DO NOT USE) ProQuest One Academic ProQuest One Academic UKI Edition ProQuest Central China ProQuest One Psychology ProQuest Central Basic MEDLINE - Academic PubMed Central (Full Participant titles) |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) Publicly Available Content Database ProQuest One Psychology ProQuest Central Student ProQuest One Academic Middle East (New) ProQuest Central Essentials ProQuest Health & Medical Complete (Alumni) ProQuest Central (Alumni Edition) ProQuest One Community College ProQuest One Health & Nursing ProQuest Central China ProQuest Central Health Research Premium Collection Health and Medicine Complete (Alumni Edition) ProQuest Central Korea Health & Medical Research Collection ProQuest Central (New) ProQuest Medical Library (Alumni) ProQuest Central Basic ProQuest One Academic Eastern Edition ProQuest Hospital Collection Health Research Premium Collection (Alumni) ProQuest Psychology Journals (Alumni) Neurosciences Abstracts ProQuest Hospital Collection (Alumni) ProQuest Health & Medical Complete ProQuest Medical Library ProQuest Psychology Journals ProQuest One Academic UKI Edition ProQuest One Academic ProQuest One Academic (New) ProQuest Central (Alumni) MEDLINE - Academic |
DatabaseTitleList | Neurosciences Abstracts MEDLINE - Academic Publicly Available Content Database MEDLINE |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database – sequence: 3 dbid: BENPR name: ProQuest Central url: https://www.proquest.com/central sourceTypes: Aggregation Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine |
EISSN | 1471-244X |
EndPage | 174 |
ExternalDocumentID | PMC4065391 oai_biomedcentral_com_1471_244X_14_174 3344650961 A539592039 24924233 10_1186_1471_244X_14_174 |
Genre | Research Support, Non-U.S. Gov't Journal Article |
GroupedDBID | --- 0R~ 23N 2WC 4.4 53G 5VS 6J9 7X7 88E 8FI 8FJ AAFWJ AAJSJ AASML AAYXX ABDBF ABIVO ABUWG ACGFO ACGFS ACIHN ACPRK ACUHS ADBBV ADRAZ ADUKV AEAQA AENEX AFKRA AFPKN AHBYD AHMBA AHSBF AHYZX ALIPV ALMA_UNASSIGNED_HOLDINGS AMKLP AMTXH AOIJS AZQEC BAPOH BAWUL BCNDV BENPR BFQNJ BMC BPHCQ BVXVI C6C CCPQU CITATION CS3 DIK DWQXO E3Z EAD EAP EAS EBD EBLON EBS EJD EMB EMK EMOBN ESX F5P FYUFA GNUQQ GROUPED_DOAJ GX1 H13 HMCUK HYE IAO IHR INH INR IPNFZ IPY ITC KQ8 M1P M2M M48 M~E O5R O5S OK1 OVT P2P PGMZT PHGZM PHGZT PIMPY PQQKQ PROAC PSQYO PSYQQ RBZ RIG RNS ROL RPM RSV SMD SOJ SV3 TR2 TUS UKHRP W2D WOQ WOW XSB CGR CUY CVF ECM EIF NPM PJZUB PPXIY PMFND 3V. 7TK 7XB 8FK K9. PKEHL PQEST PQUKI PRINS Q9U 7X8 -A0 ABVAZ ACRMQ ADINQ AFGXO AFNRJ C24 5PM |
ID | FETCH-LOGICAL-b584t-2d9b74496bd60f05a8bab3e1afb7c823f5ff8202dd719c5f0eed2541d65e14233 |
IEDL.DBID | RBZ |
ISSN | 1471-244X |
IngestDate | Thu Aug 21 18:27:18 EDT 2025 Wed May 22 07:12:31 EDT 2024 Mon Jul 21 10:53:12 EDT 2025 Fri Jul 11 04:15:51 EDT 2025 Fri Jul 25 01:54:16 EDT 2025 Tue Jun 17 22:04:47 EDT 2025 Tue Jun 10 21:02:47 EDT 2025 Mon Jul 21 05:57:09 EDT 2025 Thu Apr 24 23:01:34 EDT 2025 Tue Jul 01 01:46:22 EDT 2025 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 1 |
Language | English |
License | This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-b584t-2d9b74496bd60f05a8bab3e1afb7c823f5ff8202dd719c5f0eed2541d65e14233 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 ObjectType-Article-2 ObjectType-Feature-1 |
OpenAccessLink | http://dx.doi.org/10.1186/1471-244X-14-174 |
PMID | 24924233 |
PQID | 1539203334 |
PQPubID | 44775 |
PageCount | 1 |
ParticipantIDs | pubmedcentral_primary_oai_pubmedcentral_nih_gov_4065391 biomedcentral_primary_oai_biomedcentral_com_1471_244X_14_174 proquest_miscellaneous_1544013079 proquest_miscellaneous_1539707837 proquest_journals_1539203334 gale_infotracmisc_A539592039 gale_infotracacademiconefile_A539592039 pubmed_primary_24924233 crossref_primary_10_1186_1471_244X_14_174 crossref_citationtrail_10_1186_1471_244X_14_174 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2014-06-13 |
PublicationDateYYYYMMDD | 2014-06-13 |
PublicationDate_xml | – month: 06 year: 2014 text: 2014-06-13 day: 13 |
PublicationDecade | 2010 |
PublicationPlace | England |
PublicationPlace_xml | – name: England – name: London |
PublicationTitle | BMC psychiatry |
PublicationTitleAlternate | BMC Psychiatry |
PublicationYear | 2014 |
Publisher | BioMed Central Ltd BioMed Central |
Publisher_xml | – name: BioMed Central Ltd – name: BioMed Central |
References | RM Carney (1671_CR11) 2003; 54 H Baumeister (1671_CR3) 2012; 139 JC Barefoot (1671_CR9) 1996; 93 S Win (1671_CR14) 2011; 97 J Wellmann (1671_CR23) 2004; 11 S Aschenbrenner (1671_CR33) 2000 S Ye (1671_CR13) 2013; 61 JR Burnett (1671_CR6) 2004; 25 HJ Grabe (1671_CR29) 2012; 39 KW Davidson (1671_CR8) 2005; 67 B Sundermann (1671_CR41) 2014; 35 DJ Buysse (1671_CR25) 1989; 28 L Elderon (1671_CR16) 2013; 55 H Wersching (1671_CR18) 2012; 55 R Ruscheweyh (1671_CR28) 2012; 153 R Rabin (1671_CR31) 2001; 33 DL Hare (1671_CR1) 2014; 35 PS Sachdev (1671_CR40) 2009; 30 M Hamilton (1671_CR21) 1960; 23 P Libby (1671_CR5) 2011; 473 K Berger (1671_CR24) 2012; 55 A Rush (1671_CR20) 1986; 18 J Prochaska (1671_CR30) 1997; 12 J Tiffin (1671_CR36) 1948; 32 M Hamilton (1671_CR22) 1959; 32 C Gasse (1671_CR17) 2014; 21 LS Radloff (1671_CR26) 1977; 1 BT Baune (1671_CR4) 2012; 34 U Dannlowski (1671_CR37) 2009; 12 BT Baune (1671_CR12) 2012; 2 R Reitan (1671_CR35) 1958; 8 C Mathers (1671_CR2) 2008 S Debette (1671_CR38) 2010; 341 LL Herrmann (1671_CR7) 2008; 79 M Ackenheil (1671_CR19) 1999 V Pfaffenrath (1671_CR27) 2009; 29 A Nicholson (1671_CR10) 2006; 27 LH Kuller (1671_CR39) 2007; 28 W Oswald (1671_CR34) 1997 JA Blumenthal (1671_CR15) 2013; 61 J Kissler (1671_CR32) 2006; 156 13638508 - Br J Med Psychol. 1959;32(1):50-5 11491192 - Ann Med. 2001 Jul;33(5):337-43 8640971 - Circulation. 1996 Jun 1;93(11):1976-80 18867059 - J Appl Psychol. 1948 Jun;32(3):234-47 23290546 - J Am Coll Cardiol. 2013 Feb 12;61(6):631-4 22771109 - Gen Hosp Psychiatry. 2012 Sep-Oct;34(5):478-92 15167206 - Eur J Cardiovasc Prev Rehabil. 2004 Feb;11(1):48-55 22832857 - Transl Psychiatry. 2012;2:e92 22422160 - Psychiatr Prax. 2012 Apr;39(3):109-15 14399272 - J Neurol Neurosurg Psychiatry. 1960 Feb;23:56-62 17015079 - Prog Brain Res. 2006;156:147-83 17717021 - J Neurol Neurosurg Psychiatry. 2008 Jun;79(6):619-24 24282187 - Eur Heart J. 2014 Jun 1;35(21):1365-72 10170434 - Am J Health Promot. 1997 Sep-Oct;12(1):38-48 16857296 - Neurobiol Aging. 2007 Sep;28(9):1307-15 22541722 - Pain. 2012 Jun;153(6):1210-8 21339320 - Heart. 2011 Mar;97(6):500-5 23155197 - Eur J Prev Cardiol. 2014 May;21(5):532-40 18544183 - Int J Neuropsychopharmacol. 2009 Feb;12(1):11-22 24029388 - AJNR Am J Neuroradiol. 2014 May;35(5):848-55 18516207 - Clin Biochem Rev. 2004 Feb;25(1):2 21885128 - J Affect Disord. 2012 Jul;139(2):126-40 20660506 - BMJ. 2010;341:c3666 23621961 - Prog Cardiovasc Dis. 2013 May-Jun;55(6):511-23 22736161 - Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2012 Jun;55(6-7):816-21 15953804 - Psychosom Med. 2005 May-Jun;67 Suppl 1:S6-9 12893100 - Biol Psychiatry. 2003 Aug 1;54(3):241-7 2748771 - Psychiatry Res. 1989 May;28(2):193-213 23290548 - J Am Coll Cardiol. 2013 Feb 12;61(6):622-30 21593864 - Nature. 2011 May 19;473(7347):317-25 3737788 - Psychiatry Res. 1986 May;18(1):65-87 22736162 - Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2012 Jun;55(6-7):822-3 18771491 - Cephalalgia. 2009 Jan;29(1):48-57 17082208 - Eur Heart J. 2006 Dec;27(23):2763-74 17950492 - Neurobiol Aging. 2009 Jun;30(6):946-56 |
References_xml | – volume: 97 start-page: 500 year: 2011 ident: 1671_CR14 publication-title: Heart doi: 10.1136/hrt.2010.209767 – volume: 34 start-page: 478 year: 2012 ident: 1671_CR4 publication-title: Gen Hosp Psychiatry doi: 10.1016/j.genhosppsych.2012.05.013 – volume: 153 start-page: 1210 year: 2012 ident: 1671_CR28 publication-title: Pain doi: 10.1016/j.pain.2012.02.025 – volume: 33 start-page: 337 year: 2001 ident: 1671_CR31 publication-title: Ann Med doi: 10.3109/07853890109002087 – volume: 156 start-page: 147 year: 2006 ident: 1671_CR32 publication-title: Prog Brain Res doi: 10.1016/S0079-6123(06)56008-X – volume: 55 start-page: 816 year: 2012 ident: 1671_CR24 publication-title: Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz doi: 10.1007/s00103-012-1492-5 – volume: 55 start-page: 822 year: 2012 ident: 1671_CR18 publication-title: Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz doi: 10.1007/s00103-012-1491-6 – volume: 8 start-page: 271 year: 1958 ident: 1671_CR35 publication-title: Percept Mot Skills doi: 10.2466/PMS.8.7.271-276 – volume: 35 start-page: 848 issue: 5 year: 2014 ident: 1671_CR41 publication-title: AJNR Am J Neuroradiol doi: 10.3174/ajnr.A3713 – volume-title: The Global Burden of Disease: 2004 Update year: 2008 ident: 1671_CR2 doi: 10.1016/B978-012373960-5.00335-X – volume: 67 start-page: S6 issue: Suppl 1 year: 2005 ident: 1671_CR8 publication-title: Psychosom Med doi: 10.1097/01.psy.0000162257.19266.fc – volume: 28 start-page: 193 year: 1989 ident: 1671_CR25 publication-title: Psychiatry Res doi: 10.1016/0165-1781(89)90047-4 – volume: 12 start-page: 11 year: 2009 ident: 1671_CR37 publication-title: Int J Neuropsychopharmacol doi: 10.1017/S1461145708008973 – volume: 55 start-page: 511 year: 2013 ident: 1671_CR16 publication-title: Prog Cardiovasc Dis doi: 10.1016/j.pcad.2013.03.010 – volume: 25 start-page: 2 year: 2004 ident: 1671_CR6 publication-title: Clin Biochem Rev – volume-title: M.I.N.I. Mini International Neuropsychiatric Interview (German version 5.0.0, DSM-IV) year: 1999 ident: 1671_CR19 – volume: 93 start-page: 1976 year: 1996 ident: 1671_CR9 publication-title: Circulation doi: 10.1161/01.CIR.93.11.1976 – volume: 139 start-page: 126 year: 2012 ident: 1671_CR3 publication-title: J Affect Disord doi: 10.1016/j.jad.2011.05.025 – volume: 27 start-page: 2763 year: 2006 ident: 1671_CR10 publication-title: Eur Heart J doi: 10.1093/eurheartj/ehl338 – volume: 35 start-page: 1365 issue: 21 year: 2014 ident: 1671_CR1 publication-title: Eur Heart J doi: 10.1093/eurheartj/eht462 – volume: 32 start-page: 234 year: 1948 ident: 1671_CR36 publication-title: J Appl Psychol doi: 10.1037/h0061266 – volume: 18 start-page: 65 year: 1986 ident: 1671_CR20 publication-title: Psychiatry Res doi: 10.1016/0165-1781(86)90060-0 – volume: 28 start-page: 1307 year: 2007 ident: 1671_CR39 publication-title: Neurobiol Aging doi: 10.1016/j.neurobiolaging.2006.06.010 – volume: 29 start-page: 48 year: 2009 ident: 1671_CR27 publication-title: Cephalalgia doi: 10.1111/j.1468-2982.2008.01699.x – volume: 21 start-page: 532 issue: 5 year: 2014 ident: 1671_CR17 publication-title: Eur J Prev Cardiol doi: 10.1177/2047487312467874 – volume: 473 start-page: 317 year: 2011 ident: 1671_CR5 publication-title: Nature doi: 10.1038/nature10146 – volume: 2 start-page: e92 year: 2012 ident: 1671_CR12 publication-title: Transl Psychiatry doi: 10.1038/tp.2012.18 – volume: 61 start-page: 622 year: 2013 ident: 1671_CR13 publication-title: J Am Coll Cardiol doi: 10.1016/j.jacc.2012.09.058 – volume: 54 start-page: 241 year: 2003 ident: 1671_CR11 publication-title: Biol Psychiatry doi: 10.1016/S0006-3223(03)00111-2 – volume: 1 start-page: 385 year: 1977 ident: 1671_CR26 publication-title: Appl Psychol Meas doi: 10.1177/014662167700100306 – volume: 23 start-page: 56 year: 1960 ident: 1671_CR21 publication-title: J Neurol Neurosurg Psychiatry doi: 10.1136/jnnp.23.1.56 – volume: 79 start-page: 619 year: 2008 ident: 1671_CR7 publication-title: J Neurol Neurosurg Psychiatry doi: 10.1136/jnnp.2007.124651 – volume: 39 start-page: 109 year: 2012 ident: 1671_CR29 publication-title: Psychiatr Prax doi: 10.1055/s-0031-1298984 – volume: 30 start-page: 946 year: 2009 ident: 1671_CR40 publication-title: Neurobiol Aging doi: 10.1016/j.neurobiolaging.2007.08.023 – volume: 32 start-page: 50 year: 1959 ident: 1671_CR22 publication-title: Br J Med Psychol doi: 10.1111/j.2044-8341.1959.tb00467.x – volume: 341 start-page: c3666 year: 2010 ident: 1671_CR38 publication-title: BMJ doi: 10.1136/bmj.c3666 – volume: 12 start-page: 38 year: 1997 ident: 1671_CR30 publication-title: Am J Heal Promot doi: 10.4278/0890-1171-12.1.38 – volume: 61 start-page: 631 year: 2013 ident: 1671_CR15 publication-title: J Am Coll Cardiol doi: 10.1016/j.jacc.2012.11.029 – volume: 11 start-page: 48 year: 2004 ident: 1671_CR23 publication-title: Eur J Cardiovasc Prev Rehabil doi: 10.1097/01.hjr.0000118174.70522.20 – volume-title: Regensburger Wortflüssigkeits-Test year: 2000 ident: 1671_CR33 – volume-title: Nürnberger-Alters-Inventar year: 1997 ident: 1671_CR34 – reference: 22736162 - Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2012 Jun;55(6-7):822-3 – reference: 15167206 - Eur J Cardiovasc Prev Rehabil. 2004 Feb;11(1):48-55 – reference: 23621961 - Prog Cardiovasc Dis. 2013 May-Jun;55(6):511-23 – reference: 14399272 - J Neurol Neurosurg Psychiatry. 1960 Feb;23:56-62 – reference: 23155197 - Eur J Prev Cardiol. 2014 May;21(5):532-40 – reference: 18544183 - Int J Neuropsychopharmacol. 2009 Feb;12(1):11-22 – reference: 21885128 - J Affect Disord. 2012 Jul;139(2):126-40 – reference: 18516207 - Clin Biochem Rev. 2004 Feb;25(1):2 – reference: 22771109 - Gen Hosp Psychiatry. 2012 Sep-Oct;34(5):478-92 – reference: 18867059 - J Appl Psychol. 1948 Jun;32(3):234-47 – reference: 12893100 - Biol Psychiatry. 2003 Aug 1;54(3):241-7 – reference: 18771491 - Cephalalgia. 2009 Jan;29(1):48-57 – reference: 10170434 - Am J Health Promot. 1997 Sep-Oct;12(1):38-48 – reference: 20660506 - BMJ. 2010;341:c3666 – reference: 2748771 - Psychiatry Res. 1989 May;28(2):193-213 – reference: 17717021 - J Neurol Neurosurg Psychiatry. 2008 Jun;79(6):619-24 – reference: 17082208 - Eur Heart J. 2006 Dec;27(23):2763-74 – reference: 11491192 - Ann Med. 2001 Jul;33(5):337-43 – reference: 13638508 - Br J Med Psychol. 1959;32(1):50-5 – reference: 24282187 - Eur Heart J. 2014 Jun 1;35(21):1365-72 – reference: 17950492 - Neurobiol Aging. 2009 Jun;30(6):946-56 – reference: 23290546 - J Am Coll Cardiol. 2013 Feb 12;61(6):631-4 – reference: 23290548 - J Am Coll Cardiol. 2013 Feb 12;61(6):622-30 – reference: 15953804 - Psychosom Med. 2005 May-Jun;67 Suppl 1:S6-9 – reference: 17015079 - Prog Brain Res. 2006;156:147-83 – reference: 16857296 - Neurobiol Aging. 2007 Sep;28(9):1307-15 – reference: 22736161 - Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2012 Jun;55(6-7):816-21 – reference: 22832857 - Transl Psychiatry. 2012;2:e92 – reference: 21593864 - Nature. 2011 May 19;473(7347):317-25 – reference: 3737788 - Psychiatry Res. 1986 May;18(1):65-87 – reference: 21339320 - Heart. 2011 Mar;97(6):500-5 – reference: 22541722 - Pain. 2012 Jun;153(6):1210-8 – reference: 22422160 - Psychiatr Prax. 2012 Apr;39(3):109-15 – reference: 24029388 - AJNR Am J Neuroradiol. 2014 May;35(5):848-55 – reference: 8640971 - Circulation. 1996 Jun 1;93(11):1976-80 |
SSID | ssj0017851 |
Score | 2.3259432 |
Snippet | Depression and cardiovascular diseases due to arteriosclerosis are both frequent and impairing conditions. Depression and (subclinical) arteriosclerosis appear... Background Depression and cardiovascular diseases due to arteriosclerosis are both frequent and impairing conditions. Depression and (subclinical)... Doc number: 174 Abstract Background: Depression and cardiovascular diseases due to arteriosclerosis are both frequent and impairing conditions. Depression and... Background: Depression and cardiovascular diseases due to arteriosclerosis are both frequent and impairing conditions. Depression and (subclinical)... BACKGROUND: Depression and cardiovascular diseases due to arteriosclerosis are both frequent and impairing conditions. Depression and (subclinical)... |
SourceID | pubmedcentral biomedcentral proquest gale pubmed crossref |
SourceType | Open Access Repository Aggregation Database Index Database Enrichment Source |
StartPage | 174 |
SubjectTerms | Adult Age Aged Analysis Arteriosclerosis - epidemiology Asymptomatic Diseases - epidemiology Behavior Brain Brain research Cardiovascular disease Carotid Intima-Media Thickness Comorbidity Depression, Mental Depressive Disorder - epidemiology Emotions Female Gender Heart Humans Male Medical imaging Middle Aged Mortality Prospective Studies Psychiatry Quality of Life Risk Factors Social integration Stroke Studies Study Protocol Surveys and Questionnaires |
SummonAdditionalLinks | – databaseName: ProQuest Health & Medical Collection dbid: 7X7 link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV3di9QwEA96gvgifls9JYIgwoVtm_QLBDnljkM4nzzYt9B8cYWjXbe7D_4z_q3OpGm9HHpvC0k2bWcyM5n88htC3qemyo3QBTNW5wyPzlhjc8dqIXhrm8aIFvOQ59_LswvxbV2sQ8JtDLDK2SZ6Q20GjTnyFazMJk855-Lz5ifDqlF4uhpKaNwl95C6DCFd1XrZcPnC8_PRZF2uMjDEDNzZmmWCZdXNO-5XkWu6aaCveagYPXnNHZ0-Ig9DHEmPJ8E_Jnds_4TcPw8n5U_J7xMI--YME4Uoj6pucl8-90e3MwjustvQANaiCyy2p21v6LhX88VJ6qGf3TDCZPDw3UgZ3YY8oj2CgYgDOfKjdEwBTQfnp__STdaVInLx1zNycXry4-sZC7UYmIIQZcdy06hKiKZUpkxdWrS1ahW3WetUpeucu8I5CCZyY6qs0YVLwffC3jMzZWEzCNn4c3LQD719SShy3kOc6pxooUPKG2OcSq3jRpc21S4hnyKxyM3EuyGRCTtuAQWRKFWJUoVfEqSakNUsRakDzzmW27iSfr9Tl_8Y8XEZMc_1_74fUDEkLn_4V92GWwzwakikJY9BTQtU1CYhh1FPWLY6bp5VSwazMcq_Sp6Qd0szjkQoXG-H_dQHKZp4dVsfgfvmtIJpXkzaurwZUkSiQBJSRXocfea4pe8uPfG48ETG2avbH_01eQBRpUA8XcYPycFuu7dvIHLbqbd-ef4BjPVHfA priority: 102 providerName: ProQuest – databaseName: Scholars Portal Journals: Open Access dbid: M48 link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlR1daxQxMGgF8UX87mmVCIIIjd3dZL-gIlVainA-eXBvYfNFF469eh9g3_wP_gF_m7-kM9nstSmn4NvCzCSbzExmksxMCHmTmDIzQufMWJ0xvDpjtc0cq4Tgja1rIxo8hxx_LU4n4ss0n16lR4cJXG7d2uF7UpPF7P2P7xcfQeE_eIWvioMUFlgGZmrKUsHAw75N7oBdKlFNx-LqTgGfofe5RgF7uLTc0sKN7PdZZLRuLt3XbFccV3nNUJ08IPeDh0mPepF4SG7Z7hG5Ow536I_J72NwCIezJwr-H1Vtb9j8qSBdDOFxZ-05DWFcdBMw29GmM3S5VkNKJfVBoe18CZ3Bz7dL-ufnL7oIZ4x2H0gxRmTf0-m4PDSdO_8Dn9p-5aUY1XjxhExOjr99PmXhnQamwH1ZsczUqhSiLpQpEpfkTaUaxW3aOFXqKuMudw4cjcyYMq117hKwy7AvTU2R2xTcOf6U7HTzzu4SivXwwYd1TjSAkPDaGKcS67jRhU20G5HDiDHyvK_JIbFKdgwBhZXIV4l8hS8JfB2Rg4GPUoca6PgUx0z6vVBVbKF4t6EY-vo77lsUDYnCCq3qJmQ4wNCwyJY8ynmd1xmMakT2IkxQaR2DB-GSg0ZIME0I5Bz6eb0BIyWGyXV2vu5xsHwTL_-FI3BPnZTQzbNeXjcjw_KRyJARKSNJjqY5hnTtmS9KLnyR4_T5f8zXC3IP3E-BgXcp3yM7q8XavgQXb6Veec29BKcyUUE priority: 102 providerName: Scholars Portal |
Title | Establishing the bidirectional relationship between depression and subclinical arteriosclerosis – rationale, design, and characteristics of the BiDirect Study |
URI | https://www.ncbi.nlm.nih.gov/pubmed/24924233 https://www.proquest.com/docview/1539203334 https://www.proquest.com/docview/1539707837 https://www.proquest.com/docview/1544013079 http://dx.doi.org/10.1186/1471-244X-14-174 https://pubmed.ncbi.nlm.nih.gov/PMC4065391 |
Volume | 14 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1La9wwEBZNAqWX0vSVTdJFhUIpRMS25Bf0kg0bQmFDKQ0svQjrRQzBG_Zx6J_Jb82M_Gi0pL30Ygwz41ntSJqRZvSJkE-RyRMjdMqM1QnD1BkrbeJYIQSvbFkaUeE-5Owqu7wW3-bp_A9MzlYGPy6y0ximTwZOaM5iwSB-3iF7iQA_iCvzya8hY4CXzPuTRB13n5J84gtbZ9tvA5e0PTE_8kxh1eQjN3Txirzs4kd61hp8nzyzzWvyfNZlyN-Q-ymEe_3OEoXojqq6dVt-z48u--K3m_qOdkVadCiHbWjVGLraqP7AJPUln_ViBcrgx9cryuiy2z-0JyCI9R8nXkqH0M904bz6Sd3OqhQrFn-_JdcX05_nl6y7g4EpCE3WLDGlyoUoM2WyyEVpVahKcRtXTuW6SLhLnYMgIjEmj0udugh8Lqw5Y5OlNoZQjb8ju82isQeEItY9xKfOiQoYIl4a41RkHTc6s5F2I_I1MIu8a_E2JCJghxQYjBKtKtGq8CbBqiNy2ltR6g7fHK_ZuJV-nVNkT0h8GSR6XX_n_YwdQ-Kwh6_qqju9AE1DAC15lvIyLRNo1YgcB5wwXHVI7ruW7KaLlQS3g0TOQc_HgYySWALX2MWm5UFoJp7_i0fgejnKQc37trcOLUNoSDTIiORBPw7-5pDS1DcecFx4AOP48P8MdEReQLQpsM4u5sdkd73c2A8Q0a3VmOzk83xM9ibTq-8_xn5fBJ4zUYz9IH8AKs1PPg |
linkProvider | BioMedCentral |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtR3batRA9FC3oL6Id1dbHUERocMmmUmyAYu0umVru4tIC_s2JnOhgZJd94L0Z_wEv9Fzclmbon3r28LMySR77pc5B-CNZ-LASB1yY3XAKXXGExs43pdSpDZJjEwpDjkaR8NT-WUSTjbgd3MXhsoqG5lYCmoz1RQj7yFnJoEnhJAfZz84TY2i7GozQqMiiyN78RNdtsXu4WfE79sgOBicfBryeqoAz1DZLnlgkiyWMokyE3nOC9N-lmbC-qnLYt0PhAudQ7UYGBP7iQ6dh1oEvSjfRKH10fgQ-NxbsCkFujId2NwfjL9-W-ctaNR9kwztRz0fRT9HBTrhvuR-fPVW_XlLGV5VCZd0Yrte85ICPLgP92rLle1VpPYANmzxEG6P6tz8I_g1QEOziWkxtCtZllcKs4w2snlTdneWz1hdHsbWhbgFSwvDFqusuarJymLTfLrAw_Dl8wXjbF5HLu0OAlLlyU4JpdtNp9nUlcfv55U8Z1QrefEYTm8ET0-gU0wL-wwYddlHy9g5meIGTyTGuMyzThgdWU-7LnxooUXNqk4finpvt1eQJBVhVRFW8ZdCrHah12BR6bqzOg34OFelh9WP_gHxfg3RnPX_ve-IMBQJHHyqTut7E_hp1LpL7SFjhMQaSRe2WjtRUOj2ckNaqhZUC_WXrbrwer1MkFR8V9jpqtpDTaFEfN0eSZ66F-MxTytqXX8ZNaUkhHQhbtFx629urxT5WdnqXJatk_3n17_6K7gzPBkdq-PD8dELuIs2raRqPl9sQWc5X9lttBuX2cuaWRl8v2n58Afw7YY9 |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1Lb9QwELagSBUXxLsLBYyEhJBqNomdl8Slha7KoxVCVFpxseKXGrFkV_s48Gf4rcw4TthUhQu3SJ6J48x4Zmx_MybkRWTyxAidMmN1wvDojJU2cawQgle2LI2ocB_y9Cw7ORcfpuk04J8wF0b90H9gvq-3U9Bn3m7Dg_4-XhjXTvciG8dgXhk4qSmLBYP4-jq5kadpjpP0y9G3_kQBL6H3mUaBujuyvOINl3LfZwOXddlwb3muIapyy01NbpNbIb6kh61C3CHXbHOX7J6GE_R75NcxhIPdzhOF6I-qunVrfk-QLjtw3EW9oAHERXu4bEOrxtDVRnUJldRDQuv5CjqDj69XlNFl2F-0B8CI-JADz6WHpaHp3Pnuj-rW6lJENP68T84nx1_fnrBwRwNTELqsWWJKlQtRZspkkYvSqlCV4jaunMp1kXCXOgdBRmJMHpc6dRH4ZFiTxiZLbQyhHH9Adpp5Y_cIxVr4EL86JyogiHhpjFORddzozEbajcibgVjkoq3HIbFC9rAFNEWiVCVKFZ4kSHVExp0UpQ71z_Eajpn066Aiu4LjVc_R9fV32peoGBLNAupoFbIbYGhYYEseprxMywRGNSL7A0qYznrY3KmWDOZkJcEtYSPn0M_zvhk5ESLX2PmmpcHSTTz_F43A9XSUQzcPW23tR4alI1EgI5IP9Hjwm4ctTX3hC5ILX-A4fvR_AnpGdj-_m8hP788-PiY3ITAVCMmL-T7ZWS839gkEf2v11M_q38iiWn0 |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Establishing+the+bidirectional+relationship+between+depression+and+subclinical+arteriosclerosis+%E2%80%93+rationale%2C+design%2C+and+characteristics+of+the+BiDirect+Study&rft.jtitle=BMC+psychiatry&rft.au=Teismann%2C+Henning&rft.au=Wersching%2C+Heike&rft.au=Nagel%2C+Maren&rft.au=Arolt%2C+Volker&rft.date=2014-06-13&rft.issn=1471-244X&rft.eissn=1471-244X&rft.volume=14&rft.issue=1&rft_id=info:doi/10.1186%2F1471-244X-14-174&rft.externalDBID=n%2Fa&rft.externalDocID=10_1186_1471_244X_14_174 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1471-244X&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1471-244X&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1471-244X&client=summon |