Novel Biochemical Markers of Psychosocial Stress in Women

被引:67
作者
Asberg, Marie [1 ]
Nygren, Ake [1 ]
Leopardi, Rosario [2 ]
Rylander, Gunnar [2 ]
Peterson, Ulla [1 ]
Wilczek, Lukas [1 ]
Kallmen, Hakan [1 ]
Ekstedt, Mirjam [3 ,4 ]
Akerstedt, Torbjorn [3 ,4 ]
Lekander, Mats [2 ]
Ekman, Rolf [5 ]
机构
[1] Karolinska Inst, Dept Clin Sci, Stockholm, Sweden
[2] Karolinska Inst, Dept Clin Neurosci, Stockholm, Sweden
[3] Karolinska Inst, Inst Psychosocial Med, Stockholm, Sweden
[4] Karolinska Inst, Dept Publ Hlth, Stockholm, Sweden
[5] Gothenburg Univ, Inst Clin Neurosci, Gothenburg, Sweden
来源
PLOS ONE | 2009年 / 4卷 / 01期
关键词
EPIDERMAL-GROWTH-FACTOR; NF-KAPPA-B; SLEEP; CYTOKINES; PATHWAYS; CORTISOL; RHYTHMS; HEALTH; TISSUE; WORK;
D O I
10.1371/journal.pone.0003590
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Prolonged psychosocial stress is a condition assessed through self-reports. Here we aimed to identify biochemical markers for screening and early intervention in women. Methods: Plasma concentrations of interleukin (IL) 1-alpha, IL1-beta, IL-2, IL-4, IL-6, IL-8, IL-10, interferon-gamma (INF-gamma), tumor necrosis factor-alpha (TNF-alpha), monocyte chemotactic protein-1 (MCP-1), epidermal growth factor (EGF), vascular endothelial growth factor (VEGF), thyroid stimulating hormone (TSH), total tri-iodothyronine (TT3), total thyroxine (TT4), prolactin, and testosterone were measured in: 195 women on long-term sick-leave for a stress-related affective disorder, 45 women at risk for professional burnout, and 84 healthy women. Results: We found significantly increased levels of MCP-1, VEGF and EGF in women exposed to prolonged psychosocial stress. Statistical analysis indicates that they independently associate with a significant risk for being classified as ill. Conclusions: MCP-1, EGF, and VEGF are potential markers for screening and early intervention in women under prolonged psychosocial stress.
引用
收藏
页数:5
相关论文
共 39 条
[1]  
AMASYALI B, 2008, INT J CARDI IN PRESS
[2]   Cytokines, stress, and depressive illness [J].
Anisman, H ;
Merali, Z .
BRAIN BEHAVIOR AND IMMUNITY, 2002, 16 (05) :513-524
[3]   A mechanism converting psychosocial stress into mononuclear cell activation [J].
Bierhaus, A ;
Wolf, J ;
Andrassy, M ;
Rohleder, N ;
Humpert, PM ;
Petrov, D ;
Ferstl, R ;
von Eynatten, M ;
Wendt, T ;
Rudofsky, G ;
Joswig, M ;
Morcos, M ;
Schwaninger, M ;
McEwen, B ;
Kirschbaum, C ;
Nawroth, PP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (04) :1920-1925
[4]   The job demands-resources model of burnout [J].
Demerouti, E ;
Bakker, AB ;
Nachreiner, F ;
Schaufeli, WB .
JOURNAL OF APPLIED PSYCHOLOGY, 2001, 86 (03) :499-512
[5]   Molecular mechanisms mediating inflammation in vascular disease - Special reference to monocyte chemoattractant protein-1 [J].
Egashira, K .
HYPERTENSION, 2003, 41 (03) :834-841
[6]   Microarousals during sleep are associated with increased levels of lipids, cortisol, and blood pressure [J].
Ekstedt, M ;
Åkerstedt, T ;
Söderström, M .
PSYCHOSOMATIC MEDICINE, 2004, 66 (06) :925-931
[7]   Disturbed sleep and fatigue in occupational burnout [J].
Ekstedt, Miriam ;
Soderstrom, Marie ;
Akerstedt, Torbjorn ;
Nilsson, Jens ;
Sondergaard, Hans-Peter ;
Aleksander, Perski .
SCANDINAVIAN JOURNAL OF WORK ENVIRONMENT & HEALTH, 2006, 32 (02) :121-131
[8]   Neural immune pathways and their connection to inflammatory diseases [J].
Eskandari, F ;
Webster, JI ;
Sternberg, EM .
ARTHRITIS RESEARCH & THERAPY, 2003, 5 (06) :251-265
[9]  
First M.B., 1997, Structured Clinical Interviewfor DSM-IV Axis I Disorders
[10]   Development of a high-throughput automated analyzer using biochip array technology [J].
FitzGerald, SP ;
Lamont, JV ;
McConnell, RI ;
Benchikh, EO .
CLINICAL CHEMISTRY, 2005, 51 (07) :1165-1176