Prospects of studies on violence, adolescence and cortisol: a systematic literature review

Leonardo Planel Lugarinho Joviana Quintes Avanci Liana Wernersbach Pinto About the authors

Abstract

Violence has a negative impact on adolescents and affects their quality of life. It causes stress and requires the victim’s adaptive capacity, which can cause psychological and biological changes. Hormone cortisol levels have been used as stress biomarker in several studies. This paper aims to perform a systematic literature review of publications on cortisol and violence involving teenagers from 2000 to 2013. Descriptors “cortisol”, “violence” and “adolescent” were used in both English and Portuguese in this review, which included bibliographic databases PubMed/Medline, Lilacs, BVS and SciELO. Twelve papers were analyzed. Most studies involve participants from the United States, of both genders and without a control group. Different types of violence are studied, especially family violence, victimization or testimony. All studies used saliva to measure cortisol and no standard methodology was used for the analysis. Most studies (83.3%) found a statistically significant association between cortisol levels and exposure to violence. Results regarding gender, type of violence, socioeconomic status or cortisol analysis methods are not yet uniform.

Cortisol; Violence; Adolescent; Stress

Introduction

The World Health Organization11. World Health Organization (WHO). World report on violence and health. Genebra: WHO; 2002. defines violence as “the intentional use of physical force or power, threatened or actual, against oneself, another person, or against a group or community that either results in or has a high likelihood of resulting in injury, death, psychological harm, maldevelopment, or deprivation.” Violence derives from a network of diverse socioeconomic, political, and cultural factors that have great interdependence and influence the lives of individuals and/or social groups. It can affect all human beings, regardless of gender, geographical location, socioeconomic and cultural status, with significant disparities in their prevalence in different populations.

Violence is a particularly harmful and stressful event, requiring the victim’s adaptive capacity, which can lead to psychological and biological changes that, in turn, affect health22. Cohen S, Doyle WJ, Baum A. Socioeconomic status is associated with stress hormones. Psychosom Med 2006; 68(3):414-420.. Violence and stress have an intrinsic relationship, where they both provide feedback to one another, since chronic stress can lead to more violent acts and new victimizations, leading to additional stress and health problems. Miller et al.33. Miller GE, Chen E, Zhou ES. If it goes up, must it come down? Chronic stress and the hypothalamic-pituitary-adrenocortical axis in humans. Psychol Bull 2007; 133(1):25-45. warn that exposure to chronic stress increases by three to fourfold the odds of an adverse medical situation.

From the late 1980s, eminently experimental studies began to be developed on the physiological and biochemical analysis of the hypothalamic-pituitary-adrenocortical (HPA) axis, the hormone cortisol and its biological function in the body, as well as cortisol’s response on awakening and its circadian rhythm. The HPA axis is a hormonal response system activated by a series of physical or psychological stressor events. From a biological perspective, one of the objectives of this line of research is to understand how the activation of specific physiological systems modulated by physical and psychological conditions22. Cohen S, Doyle WJ, Baum A. Socioeconomic status is associated with stress hormones. Psychosom Med 2006; 68(3):414-420. occurs.

One of HPA axis’ main biochemical products is hormone cortisol, which is produced by the adrenal glands and is a great modulator of the immune response, as well as a mediator of the glycogenic chain for the quick retrieval of energy when facing a stressful situation44. Chrousos GP. The hypothalamic–pituitary–adrenal axis and immune-mediated inflammation. N Engl J Med 1995; 332(20):1351-1362.,55. Castro M, Moreira AC. Análise crítica do cortisol salivar na avaliação do eixo hipotálamo-hipófise-adrenal. Arq Bras Endocrinol Metab 2003; 47(4):358-367.. The production and secretion of cortisol grow in increasing amounts during and after exposure to some stressors. Usually, cortisol has an excellent association between its production and HPA axis activity; it is easily detected in saliva, blood and urine66. Adam EK, Kumari M. Assessing salivary cortisol in large-scale, epidemiological research. Psychoneuroendocrinology 2009; 34(10):1423-1436.. It is an excellent biomarker of HPA function and, consequently, of the study on the impact of stress in humans77. Hellhammer J, Wust S, Kudielka BM. Salivary cortisol as a biomarker in stress research. Psychoneuroendocrinology 2009; 34(2):163-171..

From this context, in the late 1990s, studies were developed in several countries where the relationship between stress and cortisol began to be investigated through reliable methods of detecting free cortisol in the body, and exposure to violence was an important issue in this research scenario. War veterans with severe emotional disorders were the particularly investigated population groups, in addition to clinical groups with mental health problems, including posttraumatic stress disorder, depression and anxiety88. Chida Y, Steptoe A. Cortisol awakening response and psychosocial factors: a systematic review and meta-analysis. Biol Psychol 2009; 80(3):265-278..

In the interface between violence and health, psychosocial problems are commonly studied, but there are few studies examining their association with physiological issues. Reflecting from the biopsychosocial approach of human development, it is important to look at how much the environment is impacting on organic (physiological, genetic, epigenetic, among others) manifestations, understanding it in a relation of interdependence. Thus, it is important for public health to understand how states of alertness and stress caused, for example, by the violence that affects children and adolescents, impact human development, therefore resulting in a social issue that must be investigated, prevented and confronted. It is also important to understand the relationship between levels of cortisol and violence in adolescence, since this moment is already characterized as a naturally more critical and stressful stage, with physical, psychological and social transformations, where polarities of courage and restrained fear, the transition to secondary education, conflicts with parents and grief and learning are evident99. Rodriguez CF. O que os jovens têm a dizer sobre a adolescência e o tema da morte? [dissertação]. São Paulo: Universidade de São Paulo; 2005.,1010. Burt C, Cohen L, Bjorck J. Perceived family environment as a moderator of young adolescents’ life stress adjustment. Am J Community Psychol 1988; 16(1):101-122.. Taking as a starting point the relevance of investigating the setting of this matter, this paper intends to present a systematic bibliographical review of national and international publications on the subject.

Methodology

This is a systematic review of the literature, which according to Greenhalgh1111. Greenhalgh T. Papers that summarise other papers (systematic reviews and metaanalyses). BMJ 1997; 315(7109):672-675. involves the elaboration of an overview of primary studies that explicitly contain their objectives, methods and materials so that they may be replicated by other authors. This review followed the guidelines proposed by the Preferred Reporting Items for Systematic Reviews and Meta-Analyses - PRISMA1212. Panic N, Leoncini E, de Belvis G, Ricciardi W, Boccia S. Evaluation of the endorsement of the preferred reporting items for systematic reviews and meta-analysis (PRISMA) statement on the quality of published systematic review and meta-analyses. PLoS One 2013; 8(12):e83138. and Amstar1313. Moher D, Liberati A, Tetzlaff J, Altman DG, PRISMA Group. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Ann Intern Med 2009; 151(4):264-269., which includes the following steps: identification of the material (search in the bibliographic bases), selection and eligibility (exclusion of duplicate records and application of exclusion criteria), and definition of publications to be analyzed (Figure 1).

Figure 1
Flowchart of the main steps of the systematic bibliographic review.

This review accessed the following bibliographic bases: BVS (Virtual Health Library), SciELO (Scientific Electronic Library Online), Lilacs (Latin American and Caribbean Health Sciences Literature) and Medline/Pubmed (Medical Literature Analysis and Retrieval System Online). Papers search was performed with same descriptors in both English and Portuguese, namely, “adolescent”, “violence” and “cortisol”. These descriptors were selected due to their recurrence in the indexing of papers on the subject. Boolean descriptor “AND” was inserted between descriptors for a better qualification of search results.

The selected timeline period of the publications analyzed in this study was 2000-2013, since studies on violence and cortisol became more frequent from the 2000s onwards. All data were collected between March and April 2014.

Table 1 shows the number of publications identified, according to the bibliographical database consulted, reaching a final number of 121 scientific papers.

Table 1
Number of scientific papers located, by bibliographic base.

In the selection stage, 32 papers were excluded due to duplication among bibliographic bases. Then, we performed partial (abstract only) or total reading of all identified papers. Partial reading was done initially and, when only the abstract was not conclusive, we proceeded with the full reading of the paper. Two independent researchers selected the papers. Discrepancies among the selected papers to be analyzed were decided by joint discussion among the researchers. At this stage, 69 articles were eliminated due to lack of adequacy to the object of research.

Then, at the eligibility stage, the following exclusion criteria were applied: (A) those that mostly included samples of children or adults, with a limit of 10 years for children and above 19 for adults; (B) those who did not include analyzes of cortisol results; and (C) those who had no methodological description for cortisol analysis. As a result, eight papers were discarded ((A) = 2; (B) = 3; and (C) = 3).

Figure 1 shows the flowchart for the identification and selection of articles for systematic review on the topic of violence in adolescence and cortisol, achieving a final result of 12 papers to be analyzed in this study.

Results

Chart 1 shows the main characteristics of the selected studies. Of the 12 publications included in this review, six papers (50.0%) were published in the last three years (2011, 2012 and 2013) and only three (25.0%) before 2006, the other three articles were published between 2006 and 2011.

Chart 1
Characteristics of studies on cortisol, violence and adolescence, by chronological order of publication (from the most recent to the oldest).

As for the populations studied, most participants were from the United States (eight papers, 66.7%), Canada (two papers, 16.7%), Sweden and the Palestinian Region (one paper each). There are no papers originating from research conducted in South America or in Portuguese. The main ways of selecting participants were from a larger study1414. Young EA, Tolman R, Witkowski K, Kaplan G. Salivary cortisol and posttraumatic stress disorder in a low-income community sample of women. Biol Psychiatry 2004; 55(6):621-626.

15. MacMillan HL, Georgiades K, Duku EK, Shea A, Steiner M, Niec A, Tanaka M, Gensey S, Spree S, Vella E, Walsh CA, De Bellis MD, Van der Meulen J, Boyle MH, Schmidt LA. Cortisol response to stress in female youths exposed to childhood maltreatment: results of the youth mood project. Biol Psychiatry 2009; 66(1):62-68.

16. Suglia SF, Staudenmayer J, Cohen S, Wright RJ. Posttraumatic stress symptoms related to community violence and children’s diurnal cortisol response in an urban community-dwelling sample. Int J Behav Med 2010; 17(1):43-50.

17. Cook EC, Chaplin TM, Sinha R, Tebes JK, Mayes LC. The stress response and adolescents adjustment: the impact of child maltreatment. J Youth Adolesc 2012; 41(8):1067-1077.
-1818. Linares LO, Shrout PE, Nucci-Sack A, Diaz A. Child maltreatment, dating perpetration of physical assault, and cortisol reactivity among disadvantaged female adolescents. Neuroendocrinology 2013; 97(3):252-259., advertising1919. Harkness KL, Stewart JG, Wynne-Edwards KE. Cortisol reactivity to social stress in adolescents: moderation by depression severity and child maltreatment. Psychoneuroendocrinology 2011; 36(2):173-181.

20. Murali R, Chen E. Exposure to violence and cardiovascular and neuroendocrine measures in adolescents. Ann Behav Med 2005; 30(2):155-163.
-2121. Saxbe DE, Margolin G, Spies Shapiro LA, Baucom BR. Does dampened physiological reactivity protect youth in aggressive family environments? Child Dev 2012; 83(3):821-830. and in health and education services2222. Peckins MK, Dockray S, Eckenrode JL, Heaton J, Susman EJ. The longitudinal impact of exposure to violence on cortisol reactivity in adolescents. J Adolesc Health 2012; 51(4):366-372.

23. Ivarsson M, Anderson M, Akersterd T, Lindblad F. Playing a violent television game does not affect saliva cortisol. Acta Paediatr 2009; 98(6):1052-1053.

24. Kliewer W. Violence Exposure and cortisol responses in urban youth. Int J Behav Med 2006; 13(2):106-120.
-2525. Victoroff J, Quota S, Adelman JR, Celinska B, Stern N, Wilcox R, Sapolsky RM. Support for religio-political aggression among teenage boys in Gaza: part II: neuroendocrinological findings. Aggress Behav 2011; 37(2):121-132.. Due to the very nature of the research object, it is difficult to use samples with strict designs. Only three studies used control groups. Most worked with a single sample, which was then subdivided into statistical analyzes in groups exposed to violence or not. Most studies included individuals of both genders (58.3%). However, three papers covered only girls1414. Young EA, Tolman R, Witkowski K, Kaplan G. Salivary cortisol and posttraumatic stress disorder in a low-income community sample of women. Biol Psychiatry 2004; 55(6):621-626.,1515. MacMillan HL, Georgiades K, Duku EK, Shea A, Steiner M, Niec A, Tanaka M, Gensey S, Spree S, Vella E, Walsh CA, De Bellis MD, Van der Meulen J, Boyle MH, Schmidt LA. Cortisol response to stress in female youths exposed to childhood maltreatment: results of the youth mood project. Biol Psychiatry 2009; 66(1):62-68.,1818. Linares LO, Shrout PE, Nucci-Sack A, Diaz A. Child maltreatment, dating perpetration of physical assault, and cortisol reactivity among disadvantaged female adolescents. Neuroendocrinology 2013; 97(3):252-259. (25.0%) and two included only males2323. Ivarsson M, Anderson M, Akersterd T, Lindblad F. Playing a violent television game does not affect saliva cortisol. Acta Paediatr 2009; 98(6):1052-1053.,2525. Victoroff J, Quota S, Adelman JR, Celinska B, Stern N, Wilcox R, Sapolsky RM. Support for religio-political aggression among teenage boys in Gaza: part II: neuroendocrinological findings. Aggress Behav 2011; 37(2):121-132. (16.7%). Regarding the age of participants, most of them worked exclusively with adolescents (five papers, 41.7%), two included children and adolescents1616. Suglia SF, Staudenmayer J, Cohen S, Wright RJ. Posttraumatic stress symptoms related to community violence and children’s diurnal cortisol response in an urban community-dwelling sample. Int J Behav Med 2010; 17(1):43-50.,2222. Peckins MK, Dockray S, Eckenrode JL, Heaton J, Susman EJ. The longitudinal impact of exposure to violence on cortisol reactivity in adolescents. J Adolesc Health 2012; 51(4):366-372. (16.7%), two adolescents and adults1414. Young EA, Tolman R, Witkowski K, Kaplan G. Salivary cortisol and posttraumatic stress disorder in a low-income community sample of women. Biol Psychiatry 2004; 55(6):621-626.,1919. Harkness KL, Stewart JG, Wynne-Edwards KE. Cortisol reactivity to social stress in adolescents: moderation by depression severity and child maltreatment. Psychoneuroendocrinology 2011; 36(2):173-181. (16.7%) and the rest reported only the average age of the participants2121. Saxbe DE, Margolin G, Spies Shapiro LA, Baucom BR. Does dampened physiological reactivity protect youth in aggressive family environments? Child Dev 2012; 83(3):821-830.,2323. Ivarsson M, Anderson M, Akersterd T, Lindblad F. Playing a violent television game does not affect saliva cortisol. Acta Paediatr 2009; 98(6):1052-1053.,2424. Kliewer W. Violence Exposure and cortisol responses in urban youth. Int J Behav Med 2006; 13(2):106-120.. In those involving children and adults, the proportion of adolescents overlapped, as foreseen in the exclusion criteria described. In this group of five adolescent-only papers, only one2525. Victoroff J, Quota S, Adelman JR, Celinska B, Stern N, Wilcox R, Sapolsky RM. Support for religio-political aggression among teenage boys in Gaza: part II: neuroendocrinological findings. Aggress Behav 2011; 37(2):121-132. selected only individuals at a fixed age (14 years of age).

Regarding the socioeconomic status of the research participants, five articles1414. Young EA, Tolman R, Witkowski K, Kaplan G. Salivary cortisol and posttraumatic stress disorder in a low-income community sample of women. Biol Psychiatry 2004; 55(6):621-626.,1717. Cook EC, Chaplin TM, Sinha R, Tebes JK, Mayes LC. The stress response and adolescents adjustment: the impact of child maltreatment. J Youth Adolesc 2012; 41(8):1067-1077.,1818. Linares LO, Shrout PE, Nucci-Sack A, Diaz A. Child maltreatment, dating perpetration of physical assault, and cortisol reactivity among disadvantaged female adolescents. Neuroendocrinology 2013; 97(3):252-259.,2424. Kliewer W. Violence Exposure and cortisol responses in urban youth. Int J Behav Med 2006; 13(2):106-120.,2525. Victoroff J, Quota S, Adelman JR, Celinska B, Stern N, Wilcox R, Sapolsky RM. Support for religio-political aggression among teenage boys in Gaza: part II: neuroendocrinological findings. Aggress Behav 2011; 37(2):121-132. (41.6%) stated that all participants were from poor regions or low-income population, quoting the average income of families in the region and/or low human development index as poverty indicators. The remaining papers analyzed comprised populations of different socioeconomic conditions, or this information was not revealed in the text of the paper.

Different types of violence are addressed in the articles analyzed. Most1414. Young EA, Tolman R, Witkowski K, Kaplan G. Salivary cortisol and posttraumatic stress disorder in a low-income community sample of women. Biol Psychiatry 2004; 55(6):621-626.,1515. MacMillan HL, Georgiades K, Duku EK, Shea A, Steiner M, Niec A, Tanaka M, Gensey S, Spree S, Vella E, Walsh CA, De Bellis MD, Van der Meulen J, Boyle MH, Schmidt LA. Cortisol response to stress in female youths exposed to childhood maltreatment: results of the youth mood project. Biol Psychiatry 2009; 66(1):62-68.,1717. Cook EC, Chaplin TM, Sinha R, Tebes JK, Mayes LC. The stress response and adolescents adjustment: the impact of child maltreatment. J Youth Adolesc 2012; 41(8):1067-1077.

18. Linares LO, Shrout PE, Nucci-Sack A, Diaz A. Child maltreatment, dating perpetration of physical assault, and cortisol reactivity among disadvantaged female adolescents. Neuroendocrinology 2013; 97(3):252-259.
-1919. Harkness KL, Stewart JG, Wynne-Edwards KE. Cortisol reactivity to social stress in adolescents: moderation by depression severity and child maltreatment. Psychoneuroendocrinology 2011; 36(2):173-181.,2121. Saxbe DE, Margolin G, Spies Shapiro LA, Baucom BR. Does dampened physiological reactivity protect youth in aggressive family environments? Child Dev 2012; 83(3):821-830.,2222. Peckins MK, Dockray S, Eckenrode JL, Heaton J, Susman EJ. The longitudinal impact of exposure to violence on cortisol reactivity in adolescents. J Adolesc Health 2012; 51(4):366-372. (58.3%) refer to family violence, where victimization or witnessing are addressed. Two studies1616. Suglia SF, Staudenmayer J, Cohen S, Wright RJ. Posttraumatic stress symptoms related to community violence and children’s diurnal cortisol response in an urban community-dwelling sample. Int J Behav Med 2010; 17(1):43-50.,2424. Kliewer W. Violence Exposure and cortisol responses in urban youth. Int J Behav Med 2006; 13(2):106-120. focus on community violence, one2525. Victoroff J, Quota S, Adelman JR, Celinska B, Stern N, Wilcox R, Sapolsky RM. Support for religio-political aggression among teenage boys in Gaza: part II: neuroendocrinological findings. Aggress Behav 2011; 37(2):121-132. on violence motivated by political and religious issues, another2323. Ivarsson M, Anderson M, Akersterd T, Lindblad F. Playing a violent television game does not affect saliva cortisol. Acta Paediatr 2009; 98(6):1052-1053. on media violence, and one2020. Murali R, Chen E. Exposure to violence and cardiovascular and neuroendocrine measures in adolescents. Ann Behav Med 2005; 30(2):155-163. that addresses witnessing of situations of violence in various contexts. The evidence of mental disorders (anxiety, depression, suicide attempt and post-traumatic stress disorder) is the most frequently addressed issue in the publications and is studied concomitantly with violence and cortisol.

Different methods are developed in the 12 articles analyzed. Most of the analyzed publications1414. Young EA, Tolman R, Witkowski K, Kaplan G. Salivary cortisol and posttraumatic stress disorder in a low-income community sample of women. Biol Psychiatry 2004; 55(6):621-626.,1515. MacMillan HL, Georgiades K, Duku EK, Shea A, Steiner M, Niec A, Tanaka M, Gensey S, Spree S, Vella E, Walsh CA, De Bellis MD, Van der Meulen J, Boyle MH, Schmidt LA. Cortisol response to stress in female youths exposed to childhood maltreatment: results of the youth mood project. Biol Psychiatry 2009; 66(1):62-68.,1717. Cook EC, Chaplin TM, Sinha R, Tebes JK, Mayes LC. The stress response and adolescents adjustment: the impact of child maltreatment. J Youth Adolesc 2012; 41(8):1067-1077.,2222. Peckins MK, Dockray S, Eckenrode JL, Heaton J, Susman EJ. The longitudinal impact of exposure to violence on cortisol reactivity in adolescents. J Adolesc Health 2012; 51(4):366-372.,2323. Ivarsson M, Anderson M, Akersterd T, Lindblad F. Playing a violent television game does not affect saliva cortisol. Acta Paediatr 2009; 98(6):1052-1053.,2626. Blackhart GC, Eckel LA, Tice DM. Salivary cortisol in response to acute social rejection and acceptance by peers. Biol Psychol 2007; 75(3):267-276. use structured and validated tools, such as the Conflict Tactic Scale1414. Young EA, Tolman R, Witkowski K, Kaplan G. Salivary cortisol and posttraumatic stress disorder in a low-income community sample of women. Biol Psychiatry 2004; 55(6):621-626., to verify an exposure to violent acts or actions suffered or perpetrated by adolescents, and the Trier Social Score Test1515. MacMillan HL, Georgiades K, Duku EK, Shea A, Steiner M, Niec A, Tanaka M, Gensey S, Spree S, Vella E, Walsh CA, De Bellis MD, Van der Meulen J, Boyle MH, Schmidt LA. Cortisol response to stress in female youths exposed to childhood maltreatment: results of the youth mood project. Biol Psychiatry 2009; 66(1):62-68.,1717. Cook EC, Chaplin TM, Sinha R, Tebes JK, Mayes LC. The stress response and adolescents adjustment: the impact of child maltreatment. J Youth Adolesc 2012; 41(8):1067-1077.,1919. Harkness KL, Stewart JG, Wynne-Edwards KE. Cortisol reactivity to social stress in adolescents: moderation by depression severity and child maltreatment. Psychoneuroendocrinology 2011; 36(2):173-181.,2222. Peckins MK, Dockray S, Eckenrode JL, Heaton J, Susman EJ. The longitudinal impact of exposure to violence on cortisol reactivity in adolescents. J Adolesc Health 2012; 51(4):366-372.. Two other applied methodological lines were the realistic laboratory simulation of violent acts, such as the screening of a movie with violent scenes or staging of actors showing a violent act, and the application of a mixed work plan, containing the realistic simulation and application of questionnaires.

Regarding the collection of cortisol, all the articles used the saliva to carry out analyzes. Collection done in the morning; in the afternoon; performed before, during and after the emergence of the stressful event; with short and long time intervals; and before and after the application of the questionnaire are some of the situations observed. Regarding the number of samples collected, it was verified that the analyzed studies used from one2020. Murali R, Chen E. Exposure to violence and cardiovascular and neuroendocrine measures in adolescents. Ann Behav Med 2005; 30(2):155-163. to 71717. Cook EC, Chaplin TM, Sinha R, Tebes JK, Mayes LC. The stress response and adolescents adjustment: the impact of child maltreatment. J Youth Adolesc 2012; 41(8):1067-1077. collections, of which four were the most usual number1414. Young EA, Tolman R, Witkowski K, Kaplan G. Salivary cortisol and posttraumatic stress disorder in a low-income community sample of women. Biol Psychiatry 2004; 55(6):621-626.,1616. Suglia SF, Staudenmayer J, Cohen S, Wright RJ. Posttraumatic stress symptoms related to community violence and children’s diurnal cortisol response in an urban community-dwelling sample. Int J Behav Med 2010; 17(1):43-50.,2323. Ivarsson M, Anderson M, Akersterd T, Lindblad F. Playing a violent television game does not affect saliva cortisol. Acta Paediatr 2009; 98(6):1052-1053.,2525. Victoroff J, Quota S, Adelman JR, Celinska B, Stern N, Wilcox R, Sapolsky RM. Support for religio-political aggression among teenage boys in Gaza: part II: neuroendocrinological findings. Aggress Behav 2011; 37(2):121-132..

Regarding cortisol analysis, most studies (75.0%) used enzyme immunoassay (ELISA) methods. Only three articles1414. Young EA, Tolman R, Witkowski K, Kaplan G. Salivary cortisol and posttraumatic stress disorder in a low-income community sample of women. Biol Psychiatry 2004; 55(6):621-626.,1616. Suglia SF, Staudenmayer J, Cohen S, Wright RJ. Posttraumatic stress symptoms related to community violence and children’s diurnal cortisol response in an urban community-dwelling sample. Int J Behav Med 2010; 17(1):43-50.,2525. Victoroff J, Quota S, Adelman JR, Celinska B, Stern N, Wilcox R, Sapolsky RM. Support for religio-political aggression among teenage boys in Gaza: part II: neuroendocrinological findings. Aggress Behav 2011; 37(2):121-132. (25.0%) used radioimmunoassay (RIA), with the affirmation that the results found are compatible with enzyme immunoassays1414. Young EA, Tolman R, Witkowski K, Kaplan G. Salivary cortisol and posttraumatic stress disorder in a low-income community sample of women. Biol Psychiatry 2004; 55(6):621-626.. Regarding the indicators of quality and analytical precision of cortisol results, different methods were used: intra-assay and inter-assay coefficients of variability1616. Suglia SF, Staudenmayer J, Cohen S, Wright RJ. Posttraumatic stress symptoms related to community violence and children’s diurnal cortisol response in an urban community-dwelling sample. Int J Behav Med 2010; 17(1):43-50.,1818. Linares LO, Shrout PE, Nucci-Sack A, Diaz A. Child maltreatment, dating perpetration of physical assault, and cortisol reactivity among disadvantaged female adolescents. Neuroendocrinology 2013; 97(3):252-259.,1919. Harkness KL, Stewart JG, Wynne-Edwards KE. Cortisol reactivity to social stress in adolescents: moderation by depression severity and child maltreatment. Psychoneuroendocrinology 2011; 36(2):173-181.,2121. Saxbe DE, Margolin G, Spies Shapiro LA, Baucom BR. Does dampened physiological reactivity protect youth in aggressive family environments? Child Dev 2012; 83(3):821-830.,2222. Peckins MK, Dockray S, Eckenrode JL, Heaton J, Susman EJ. The longitudinal impact of exposure to violence on cortisol reactivity in adolescents. J Adolesc Health 2012; 51(4):366-372.,2525. Victoroff J, Quota S, Adelman JR, Celinska B, Stern N, Wilcox R, Sapolsky RM. Support for religio-political aggression among teenage boys in Gaza: part II: neuroendocrinological findings. Aggress Behav 2011; 37(2):121-132., biochemical test sensitivity2020. Murali R, Chen E. Exposure to violence and cardiovascular and neuroendocrine measures in adolescents. Ann Behav Med 2005; 30(2):155-163.,2222. Peckins MK, Dockray S, Eckenrode JL, Heaton J, Susman EJ. The longitudinal impact of exposure to violence on cortisol reactivity in adolescents. J Adolesc Health 2012; 51(4):366-372.,2424. Kliewer W. Violence Exposure and cortisol responses in urban youth. Int J Behav Med 2006; 13(2):106-120.,2525. Victoroff J, Quota S, Adelman JR, Celinska B, Stern N, Wilcox R, Sapolsky RM. Support for religio-political aggression among teenage boys in Gaza: part II: neuroendocrinological findings. Aggress Behav 2011; 37(2):121-132. and duplicate analyzes1515. MacMillan HL, Georgiades K, Duku EK, Shea A, Steiner M, Niec A, Tanaka M, Gensey S, Spree S, Vella E, Walsh CA, De Bellis MD, Van der Meulen J, Boyle MH, Schmidt LA. Cortisol response to stress in female youths exposed to childhood maltreatment: results of the youth mood project. Biol Psychiatry 2009; 66(1):62-68.,1717. Cook EC, Chaplin TM, Sinha R, Tebes JK, Mayes LC. The stress response and adolescents adjustment: the impact of child maltreatment. J Youth Adolesc 2012; 41(8):1067-1077.,1818. Linares LO, Shrout PE, Nucci-Sack A, Diaz A. Child maltreatment, dating perpetration of physical assault, and cortisol reactivity among disadvantaged female adolescents. Neuroendocrinology 2013; 97(3):252-259.,1919. Harkness KL, Stewart JG, Wynne-Edwards KE. Cortisol reactivity to social stress in adolescents: moderation by depression severity and child maltreatment. Psychoneuroendocrinology 2011; 36(2):173-181.,2121. Saxbe DE, Margolin G, Spies Shapiro LA, Baucom BR. Does dampened physiological reactivity protect youth in aggressive family environments? Child Dev 2012; 83(3):821-830.,2222. Peckins MK, Dockray S, Eckenrode JL, Heaton J, Susman EJ. The longitudinal impact of exposure to violence on cortisol reactivity in adolescents. J Adolesc Health 2012; 51(4):366-372.. Tests repetition if the intra- or inter-assay coefficient was higher than a fixed value1414. Young EA, Tolman R, Witkowski K, Kaplan G. Salivary cortisol and posttraumatic stress disorder in a low-income community sample of women. Biol Psychiatry 2004; 55(6):621-626.,1919. Harkness KL, Stewart JG, Wynne-Edwards KE. Cortisol reactivity to social stress in adolescents: moderation by depression severity and child maltreatment. Psychoneuroendocrinology 2011; 36(2):173-181. was also mentioned, however, different cut-off points were used, without indication as to whether value used was arbitrary or based on the literature.

Regarding studies’ results, most papers (10 papers, or 83.3%) found a statistically significant association between cortisol level and exposure to violence. Of the articles describing a change in cortisol reactivity, more than half of them1414. Young EA, Tolman R, Witkowski K, Kaplan G. Salivary cortisol and posttraumatic stress disorder in a low-income community sample of women. Biol Psychiatry 2004; 55(6):621-626.,1616. Suglia SF, Staudenmayer J, Cohen S, Wright RJ. Posttraumatic stress symptoms related to community violence and children’s diurnal cortisol response in an urban community-dwelling sample. Int J Behav Med 2010; 17(1):43-50.

17. Cook EC, Chaplin TM, Sinha R, Tebes JK, Mayes LC. The stress response and adolescents adjustment: the impact of child maltreatment. J Youth Adolesc 2012; 41(8):1067-1077.

18. Linares LO, Shrout PE, Nucci-Sack A, Diaz A. Child maltreatment, dating perpetration of physical assault, and cortisol reactivity among disadvantaged female adolescents. Neuroendocrinology 2013; 97(3):252-259.

19. Harkness KL, Stewart JG, Wynne-Edwards KE. Cortisol reactivity to social stress in adolescents: moderation by depression severity and child maltreatment. Psychoneuroendocrinology 2011; 36(2):173-181.
-2020. Murali R, Chen E. Exposure to violence and cardiovascular and neuroendocrine measures in adolescents. Ann Behav Med 2005; 30(2):155-163. (60,0%, 6 articles) found increased cortisol levels in adolescents exposed to violence and four articles1515. MacMillan HL, Georgiades K, Duku EK, Shea A, Steiner M, Niec A, Tanaka M, Gensey S, Spree S, Vella E, Walsh CA, De Bellis MD, Van der Meulen J, Boyle MH, Schmidt LA. Cortisol response to stress in female youths exposed to childhood maltreatment: results of the youth mood project. Biol Psychiatry 2009; 66(1):62-68.,2121. Saxbe DE, Margolin G, Spies Shapiro LA, Baucom BR. Does dampened physiological reactivity protect youth in aggressive family environments? Child Dev 2012; 83(3):821-830.,2222. Peckins MK, Dockray S, Eckenrode JL, Heaton J, Susman EJ. The longitudinal impact of exposure to violence on cortisol reactivity in adolescents. J Adolesc Health 2012; 51(4):366-372.,2424. Kliewer W. Violence Exposure and cortisol responses in urban youth. Int J Behav Med 2006; 13(2):106-120. (40,0%) showed a decrease in the level of cortisol. Two publications2323. Ivarsson M, Anderson M, Akersterd T, Lindblad F. Playing a violent television game does not affect saliva cortisol. Acta Paediatr 2009; 98(6):1052-1053.,2525. Victoroff J, Quota S, Adelman JR, Celinska B, Stern N, Wilcox R, Sapolsky RM. Support for religio-political aggression among teenage boys in Gaza: part II: neuroendocrinological findings. Aggress Behav 2011; 37(2):121-132. reported no changes in hormone levels. Saxbe2121. Saxbe DE, Margolin G, Spies Shapiro LA, Baucom BR. Does dampened physiological reactivity protect youth in aggressive family environments? Child Dev 2012; 83(3):821-830. highlights the cumulative effect of prior history of family violence in association with cortisol levels. It is worth mentioning that the expression of cortisol varied between males and females in two studies2222. Peckins MK, Dockray S, Eckenrode JL, Heaton J, Susman EJ. The longitudinal impact of exposure to violence on cortisol reactivity in adolescents. J Adolesc Health 2012; 51(4):366-372.,2424. Kliewer W. Violence Exposure and cortisol responses in urban youth. Int J Behav Med 2006; 13(2):106-120.. However, it should be noted that not all studies included both genders in the sample.

Discussion

This literature review on cortisol and violence involving adolescents is unprecedented nationally and internationally, and shows the methodological trend and the main findings of studies on the subject. Their analysis shows the growing interest and knowledge of the international scientific community, starting in the 2000s, on the relation of the subject, with a clear highlight on the largest volume of publications in recent years, especially in the United States, which points to a certain unprecedented topic worldwide. It is worth highlighting the growing trend of more sophisticated protocols developed and the use of more robust methods. This setting increases the knowledge on the subject and leads to more reliable results66. Adam EK, Kumari M. Assessing salivary cortisol in large-scale, epidemiological research. Psychoneuroendocrinology 2009; 34(10):1423-1436.,1717. Cook EC, Chaplin TM, Sinha R, Tebes JK, Mayes LC. The stress response and adolescents adjustment: the impact of child maltreatment. J Youth Adolesc 2012; 41(8):1067-1077..

In general, this literature review clearly shows the following methodological trend in the articles analyzed: the use of saliva as the main source for cortisol analysis, the duplication of saliva collection, the collection of several samples from the same person during one day, the use of enzyme immunoassay in cortisol analysis and the subject’s exposure to a realistic and laboratory-produced situation.

The methodological options used are directly related to the scope of the research, the financial budget and the availability of participants. For example, a very critical aspect is in relation to the number of collections from the same individual. The higher the number of samples, the greater the reliability of the study. Another point that evidences great variation between studies refers to the period of collection during the day, whether in the morning or in the afternoon, which induces the lack of consensus regarding the most appropriate moment for collection. The option to perform the afternoon collection seems to be the most indicated and is justified by the lower cortisol variation in this period of the day1717. Cook EC, Chaplin TM, Sinha R, Tebes JK, Mayes LC. The stress response and adolescents adjustment: the impact of child maltreatment. J Youth Adolesc 2012; 41(8):1067-1077.,1818. Linares LO, Shrout PE, Nucci-Sack A, Diaz A. Child maltreatment, dating perpetration of physical assault, and cortisol reactivity among disadvantaged female adolescents. Neuroendocrinology 2013; 97(3):252-259.,2626. Blackhart GC, Eckel LA, Tice DM. Salivary cortisol in response to acute social rejection and acceptance by peers. Biol Psychol 2007; 75(3):267-276..

Although most articles demonstrate that there is a change in cortisol levels in adolescents who are victims of violence, they differ enormously when compared by chronicity, intensity and types of violence situations, as well as methodological aspects. There is no consensus on the direction of the association between exposure to violence and cortisol levels, and different explanations are given for increased and reduced levels of the hormone. One of the most accepted arguments for the diversity of results in the relationship between violence and cortisol lies in the fact that studies do not take into account the particular expression of each individual about their life experience and the stressful episodes1919. Harkness KL, Stewart JG, Wynne-Edwards KE. Cortisol reactivity to social stress in adolescents: moderation by depression severity and child maltreatment. Psychoneuroendocrinology 2011; 36(2):173-181..Other authors state that individuals only express significant physiological changes after some exposure to a major stressing situation88. Chida Y, Steptoe A. Cortisol awakening response and psychosocial factors: a systematic review and meta-analysis. Biol Psychol 2009; 80(3):265-278.. The explanation of the positive association is due to the abrupt activation of the biological response to the stressful situation, which, in the long run, is no longer protective and can become toxic to the metabolism77. Hellhammer J, Wust S, Kudielka BM. Salivary cortisol as a biomarker in stress research. Psychoneuroendocrinology 2009; 34(2):163-171.. On the other hand, scholars explain that the reduction of cortisol levels in victims of violence can generate a phenomenon called hypocortisolism, which may represent an individual’s poor adaptation to deal with a situation of threat and cause future health problems2727. Henry JP. Psychological and physiological responses to stress: The right hemisphere and the hypo-thalamo-pituitary-adrenal axis. An inquiry into problems of human bonding. Integr Physiol Behav Sci 1993, 28(4):368-387.,2828. Gunnar MR, Vazquez DM. Low cortisol and a flattening of expected daytime rhythm: Potential indices of risk in human development. Dev Psychopathol 2001; 13(3):515-538.. Heim et al.2929. Heim C, Newport DJ, Bonsall R, Miller AH, Nemeroff CB. Altered pituitary-adrenal axis responses to provocative challenge tests in adult survivors of childhood abuse. Am J Psychiatry 2001; 158(4):575-581. further add that early life stress can alter the response to stress, with a cumulative effect with acute and current stressful situations. Thus, Yehuda & Seckl3030. Yehuda R, Seckl J. Stress-related psychiatric disorders with low cortisol levels: a metabolic hypothesis. Endocrinology 2011; 152(12):4496-4503. hypothesize about a negative feedback system of the HPA axis, which could cause a change in glucocorticoid catabolism as adaptation to higher levels of cortisol at some earlier stage of life.

It is interesting to note that, in this review, the two papers that differ most from the others in relation to the type of violence (religious and virtual) were not associated with changes in cortisol levels. The non-association between adolescent exposure to realistic simulations of violent videogames and cortisol alteration may be related to the lack of stress in the situation, which can often be a pleasurable and unrealistic activity to adolescents. Another argument is that, in violent videogames, the teenage player is the perpetrator of the violent act and is rarely victimized, which produces an inverse relationship between violence and cortisol levels. In relation to religious violence, Victoroff et al.2525. Victoroff J, Quota S, Adelman JR, Celinska B, Stern N, Wilcox R, Sapolsky RM. Support for religio-political aggression among teenage boys in Gaza: part II: neuroendocrinological findings. Aggress Behav 2011; 37(2):121-132. point out the need for further studies in order to understand how aspects of human development, innate psychological factors and exposure to prolonged stress from conflicts between religious groups interact with biological issues.

It is worth mentioning that being male or female is an important issue to be considered in research on violence and cortisol. Kliewer2424. Kliewer W. Violence Exposure and cortisol responses in urban youth. Int J Behav Med 2006; 13(2):106-120. explains that boys who engage in violent situations tend to worry more than girls do with negative ratings directed at them and have more concerns about the possible loss of relationships. Compared to girls, they tend to have fewer protective resources and internal resources to deal with situations of violence. Regarding the witnessing of violence, the meaning is also different for boys and girls and, consequently, their processing. Witnessing violence seems to affect adolescents in the way social information is processed, whereas direct victimization seems to affect the adjustment of young people by means of emotional deregulation2424. Kliewer W. Violence Exposure and cortisol responses in urban youth. Int J Behav Med 2006; 13(2):106-120.. Harkness et al.1919. Harkness KL, Stewart JG, Wynne-Edwards KE. Cortisol reactivity to social stress in adolescents: moderation by depression severity and child maltreatment. Psychoneuroendocrinology 2011; 36(2):173-181. further add that mental health problems, such as depression, can mediate the relationship between violence and cortisol for underlying biological, personal, and social issues.

Another factor that draws attention in studies on cortisol and violence in adolescents is the use of samples from population groups with low socioeconomic status1414. Young EA, Tolman R, Witkowski K, Kaplan G. Salivary cortisol and posttraumatic stress disorder in a low-income community sample of women. Biol Psychiatry 2004; 55(6):621-626.,1717. Cook EC, Chaplin TM, Sinha R, Tebes JK, Mayes LC. The stress response and adolescents adjustment: the impact of child maltreatment. J Youth Adolesc 2012; 41(8):1067-1077.,1818. Linares LO, Shrout PE, Nucci-Sack A, Diaz A. Child maltreatment, dating perpetration of physical assault, and cortisol reactivity among disadvantaged female adolescents. Neuroendocrinology 2013; 97(3):252-259.,2424. Kliewer W. Violence Exposure and cortisol responses in urban youth. Int J Behav Med 2006; 13(2):106-120.,2525. Victoroff J, Quota S, Adelman JR, Celinska B, Stern N, Wilcox R, Sapolsky RM. Support for religio-political aggression among teenage boys in Gaza: part II: neuroendocrinological findings. Aggress Behav 2011; 37(2):121-132., which may result in selection bias, since these populations are more likely to face stressful situations, to have worse health and more difficulty accessing health services22. Cohen S, Doyle WJ, Baum A. Socioeconomic status is associated with stress hormones. Psychosom Med 2006; 68(3):414-420.. However, no methodological procedure was reported by authors analyzed to control possible biases.

A crosscutting issue that discusses the findings of this review is the serious biological, emotional and cognitive damage that violence can cause in the course of human development, and this is a public health issue, especially in childhood and adolescence. The National Scientific Council on the Developing Child3131. National Scientific Council on the Developing Child. Excessive Stress Disrupts the architecture of the Developing Brain: working paper # 3. 2005 [acessado 2016 jan 28]. Disponível em: http://www.developingchild.net.
http://www.developingchild.net...
highlights that chronic alterations of the HPA (Hypothalamic-Pituitary-Adrenal) axis may affect the cerebral re-constitution of children who are developing. The toxic stress has already been shown to be associated with a deficit in the development of cerebral structures, that is, a decrease in their size; as well as changes in the biological responses to the adverse event, causing damage to the autoimmune system and greater vulnerability to the development of physical and mental diseases3131. National Scientific Council on the Developing Child. Excessive Stress Disrupts the architecture of the Developing Brain: working paper # 3. 2005 [acessado 2016 jan 28]. Disponível em: http://www.developingchild.net.
http://www.developingchild.net...

32. Boeckel MG. Ambientes familiares tóxicos: impactos da violência conjugal na vinculação entre mães e filhos, no reconhecimento de emoções e nos níveis de cortisol [tese]. Porto Alegre: Faculdade de Psicologia; 2013.
-3333. Grassi-Oliveira R. Traumatologia Desenvolvimental: o impacto da negligência na infância na memória de adultos [tese]. Porto Alegre: Faculdade de Psicologia; 2007..

Finally, the greater fragility of this work stems from the lack of standardized methods and techniques of cortisol analysis concomitant to violence, either by not explicitly explaining in the works the methodological path used or the still incipient theoretical knowledge. In addition, much of what is known about this subject derives from small samples and studies with sectional designs. More studies that use more robust techniques that combine the qualitative approach and that are developed in Latin America and in other regions of the world are required.

References

  • 1
    World Health Organization (WHO). World report on violence and health Genebra: WHO; 2002.
  • 2
    Cohen S, Doyle WJ, Baum A. Socioeconomic status is associated with stress hormones. Psychosom Med 2006; 68(3):414-420.
  • 3
    Miller GE, Chen E, Zhou ES. If it goes up, must it come down? Chronic stress and the hypothalamic-pituitary-adrenocortical axis in humans. Psychol Bull 2007; 133(1):25-45.
  • 4
    Chrousos GP. The hypothalamic–pituitary–adrenal axis and immune-mediated inflammation. N Engl J Med 1995; 332(20):1351-1362.
  • 5
    Castro M, Moreira AC. Análise crítica do cortisol salivar na avaliação do eixo hipotálamo-hipófise-adrenal. Arq Bras Endocrinol Metab 2003; 47(4):358-367.
  • 6
    Adam EK, Kumari M. Assessing salivary cortisol in large-scale, epidemiological research. Psychoneuroendocrinology 2009; 34(10):1423-1436.
  • 7
    Hellhammer J, Wust S, Kudielka BM. Salivary cortisol as a biomarker in stress research. Psychoneuroendocrinology 2009; 34(2):163-171.
  • 8
    Chida Y, Steptoe A. Cortisol awakening response and psychosocial factors: a systematic review and meta-analysis. Biol Psychol 2009; 80(3):265-278.
  • 9
    Rodriguez CF. O que os jovens têm a dizer sobre a adolescência e o tema da morte? [dissertação]. São Paulo: Universidade de São Paulo; 2005.
  • 10
    Burt C, Cohen L, Bjorck J. Perceived family environment as a moderator of young adolescents’ life stress adjustment. Am J Community Psychol 1988; 16(1):101-122.
  • 11
    Greenhalgh T. Papers that summarise other papers (systematic reviews and metaanalyses). BMJ 1997; 315(7109):672-675.
  • 12
    Panic N, Leoncini E, de Belvis G, Ricciardi W, Boccia S. Evaluation of the endorsement of the preferred reporting items for systematic reviews and meta-analysis (PRISMA) statement on the quality of published systematic review and meta-analyses. PLoS One 2013; 8(12):e83138.
  • 13
    Moher D, Liberati A, Tetzlaff J, Altman DG, PRISMA Group. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Ann Intern Med 2009; 151(4):264-269.
  • 14
    Young EA, Tolman R, Witkowski K, Kaplan G. Salivary cortisol and posttraumatic stress disorder in a low-income community sample of women. Biol Psychiatry 2004; 55(6):621-626.
  • 15
    MacMillan HL, Georgiades K, Duku EK, Shea A, Steiner M, Niec A, Tanaka M, Gensey S, Spree S, Vella E, Walsh CA, De Bellis MD, Van der Meulen J, Boyle MH, Schmidt LA. Cortisol response to stress in female youths exposed to childhood maltreatment: results of the youth mood project. Biol Psychiatry 2009; 66(1):62-68.
  • 16
    Suglia SF, Staudenmayer J, Cohen S, Wright RJ. Posttraumatic stress symptoms related to community violence and children’s diurnal cortisol response in an urban community-dwelling sample. Int J Behav Med 2010; 17(1):43-50.
  • 17
    Cook EC, Chaplin TM, Sinha R, Tebes JK, Mayes LC. The stress response and adolescents adjustment: the impact of child maltreatment. J Youth Adolesc 2012; 41(8):1067-1077.
  • 18
    Linares LO, Shrout PE, Nucci-Sack A, Diaz A. Child maltreatment, dating perpetration of physical assault, and cortisol reactivity among disadvantaged female adolescents. Neuroendocrinology 2013; 97(3):252-259.
  • 19
    Harkness KL, Stewart JG, Wynne-Edwards KE. Cortisol reactivity to social stress in adolescents: moderation by depression severity and child maltreatment. Psychoneuroendocrinology 2011; 36(2):173-181.
  • 20
    Murali R, Chen E. Exposure to violence and cardiovascular and neuroendocrine measures in adolescents. Ann Behav Med 2005; 30(2):155-163.
  • 21
    Saxbe DE, Margolin G, Spies Shapiro LA, Baucom BR. Does dampened physiological reactivity protect youth in aggressive family environments? Child Dev 2012; 83(3):821-830.
  • 22
    Peckins MK, Dockray S, Eckenrode JL, Heaton J, Susman EJ. The longitudinal impact of exposure to violence on cortisol reactivity in adolescents. J Adolesc Health 2012; 51(4):366-372.
  • 23
    Ivarsson M, Anderson M, Akersterd T, Lindblad F. Playing a violent television game does not affect saliva cortisol. Acta Paediatr 2009; 98(6):1052-1053.
  • 24
    Kliewer W. Violence Exposure and cortisol responses in urban youth. Int J Behav Med 2006; 13(2):106-120.
  • 25
    Victoroff J, Quota S, Adelman JR, Celinska B, Stern N, Wilcox R, Sapolsky RM. Support for religio-political aggression among teenage boys in Gaza: part II: neuroendocrinological findings. Aggress Behav 2011; 37(2):121-132.
  • 26
    Blackhart GC, Eckel LA, Tice DM. Salivary cortisol in response to acute social rejection and acceptance by peers. Biol Psychol 2007; 75(3):267-276.
  • 27
    Henry JP. Psychological and physiological responses to stress: The right hemisphere and the hypo-thalamo-pituitary-adrenal axis. An inquiry into problems of human bonding. Integr Physiol Behav Sci 1993, 28(4):368-387.
  • 28
    Gunnar MR, Vazquez DM. Low cortisol and a flattening of expected daytime rhythm: Potential indices of risk in human development. Dev Psychopathol 2001; 13(3):515-538.
  • 29
    Heim C, Newport DJ, Bonsall R, Miller AH, Nemeroff CB. Altered pituitary-adrenal axis responses to provocative challenge tests in adult survivors of childhood abuse. Am J Psychiatry 2001; 158(4):575-581.
  • 30
    Yehuda R, Seckl J. Stress-related psychiatric disorders with low cortisol levels: a metabolic hypothesis. Endocrinology 2011; 152(12):4496-4503.
  • 31
    National Scientific Council on the Developing Child. Excessive Stress Disrupts the architecture of the Developing Brain: working paper # 3 2005 [acessado 2016 jan 28]. Disponível em: http://www.developingchild.net
    » http://www.developingchild.net
  • 32
    Boeckel MG. Ambientes familiares tóxicos: impactos da violência conjugal na vinculação entre mães e filhos, no reconhecimento de emoções e nos níveis de cortisol [tese]. Porto Alegre: Faculdade de Psicologia; 2013.
  • 33
    Grassi-Oliveira R. Traumatologia Desenvolvimental: o impacto da negligência na infância na memória de adultos [tese]. Porto Alegre: Faculdade de Psicologia; 2007.

Publication Dates

  • Publication in this collection
    Apr 2017

History

  • Received
    21 Sept 2015
  • Reviewed
    25 May 2016
  • Accepted
    27 May 2016
ABRASCO - Associação Brasileira de Saúde Coletiva Rio de Janeiro - RJ - Brazil
E-mail: revscol@fiocruz.br