Savić, Danka

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orcid::0000-0001-5861-0045
  • Savić, Danka (8)
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Author's Bibliography

PTSD and depressive symptoms are linked to DHEAS via personality

Savić, Danka; Knežević, Goran; Matić, Gordana; Damjanović, Svetozar

(Pergamon-Elsevier Science Ltd, Oxford, 2018)

TY  - JOUR
AU  - Savić, Danka
AU  - Knežević, Goran
AU  - Matić, Gordana
AU  - Damjanović, Svetozar
PY  - 2018
UR  - http://reff.f.bg.ac.rs/handle/123456789/2691
AB  - Background Research results on dehydroepiandrosterone sulfate ester (DHEAS) in post-traumatic stress disorder (PTSD) are inconsistent. We hypothesized that personality traits could be the confounders of DHEAS levels and disease symptoms, which could in part explain the discrepancy in findings. Method: This study was a part of a broader project in which simultaneous psychological and biological in-vestigations were carried out in hospital conditions. 380 male subjects were categorized in four groups: A) current PTSD (n = 132), B) lifetime PTSD (n = 66), C) trauma controls (n = 101), and D) healthy controls (n = 81), matched by age. Results: The level of DHEAS is significantly lower in the current PTSD group than in trauma controls. All groups significantly differ in personality traits Disintegration and Neuroticism (current PTSD group having the highest scores). DHEAS is related to both PTSD and depressive symptoms; however, Structural Equation Model (SEM) shows that the relations are indirect, realized via their confounder-personality trait Disintegration. Conclusions: According to our project results, DHEAS is the second putative biomarker for trauma-related dis-orders that fails to fulfil this expectation. It appears to be more directly related to personality than to the disease symptoms (the first one being basal cortisol). Our data promote personality as a biologically based construct with seemingly important role in understanding the mental health status.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Psychoneuroendocrinology
T1  - PTSD and depressive symptoms are linked to DHEAS via personality
EP  - 33
SP  - 29
VL  - 92
DO  - 10.1016/j.psyneuen.2018.03.017
ER  - 
@article{
author = "Savić, Danka and Knežević, Goran and Matić, Gordana and Damjanović, Svetozar",
year = "2018",
abstract = "Background Research results on dehydroepiandrosterone sulfate ester (DHEAS) in post-traumatic stress disorder (PTSD) are inconsistent. We hypothesized that personality traits could be the confounders of DHEAS levels and disease symptoms, which could in part explain the discrepancy in findings. Method: This study was a part of a broader project in which simultaneous psychological and biological in-vestigations were carried out in hospital conditions. 380 male subjects were categorized in four groups: A) current PTSD (n = 132), B) lifetime PTSD (n = 66), C) trauma controls (n = 101), and D) healthy controls (n = 81), matched by age. Results: The level of DHEAS is significantly lower in the current PTSD group than in trauma controls. All groups significantly differ in personality traits Disintegration and Neuroticism (current PTSD group having the highest scores). DHEAS is related to both PTSD and depressive symptoms; however, Structural Equation Model (SEM) shows that the relations are indirect, realized via their confounder-personality trait Disintegration. Conclusions: According to our project results, DHEAS is the second putative biomarker for trauma-related dis-orders that fails to fulfil this expectation. It appears to be more directly related to personality than to the disease symptoms (the first one being basal cortisol). Our data promote personality as a biologically based construct with seemingly important role in understanding the mental health status.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Psychoneuroendocrinology",
title = "PTSD and depressive symptoms are linked to DHEAS via personality",
pages = "33-29",
volume = "92",
doi = "10.1016/j.psyneuen.2018.03.017"
}
Savić, D., Knežević, G., Matić, G.,& Damjanović, S.. (2018). PTSD and depressive symptoms are linked to DHEAS via personality. in Psychoneuroendocrinology
Pergamon-Elsevier Science Ltd, Oxford., 92, 29-33.
https://doi.org/10.1016/j.psyneuen.2018.03.017
Savić D, Knežević G, Matić G, Damjanović S. PTSD and depressive symptoms are linked to DHEAS via personality. in Psychoneuroendocrinology. 2018;92:29-33.
doi:10.1016/j.psyneuen.2018.03.017 .
Savić, Danka, Knežević, Goran, Matić, Gordana, Damjanović, Svetozar, "PTSD and depressive symptoms are linked to DHEAS via personality" in Psychoneuroendocrinology, 92 (2018):29-33,
https://doi.org/10.1016/j.psyneuen.2018.03.017 . .
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Disintegration: A reconceptualization of psychosis proneness as a personality trait separate from the Big Five

Knežević, Goran; Savić, Danka; Kutlešić, Vesna; Opačić, Goran

(Academic Press Inc Elsevier Science, San Diego, 2017)

TY  - JOUR
AU  - Knežević, Goran
AU  - Savić, Danka
AU  - Kutlešić, Vesna
AU  - Opačić, Goran
PY  - 2017
UR  - http://reff.f.bg.ac.rs/handle/123456789/2445
AB  - A nine-facet hierarchical taxonomy of "Disintegration", a trait-like disposition that causes variations in psychotic-like behavior, is proposed, along with the scales to assess it. Strong correlations were demonstrated in students (n = 466) between lower-level dimensions, independent of the assessment method. Disintegration lay beyond the Five-Factor Model (FFM) space. This finding was replicated across informant types (self, mother, and father), samples (students and a national representative sample, n = 1001), and units of analyses (facets and items). The most frequent approach to preserve the FFM taxonomy of both normal and non-normal personality variants - mapping psychotic-like phenomena onto the Openness domain - found little support in our data. Disintegration was normally distributed in the general population.
PB  - Academic Press Inc Elsevier Science, San Diego
T2  - Journal of Research in Personality
T1  - Disintegration: A reconceptualization of psychosis proneness as a personality trait separate from the Big Five
EP  - 201
SP  - 187
VL  - 70
DO  - 10.1016/j.jrp.2017.06.001
ER  - 
@article{
author = "Knežević, Goran and Savić, Danka and Kutlešić, Vesna and Opačić, Goran",
year = "2017",
abstract = "A nine-facet hierarchical taxonomy of "Disintegration", a trait-like disposition that causes variations in psychotic-like behavior, is proposed, along with the scales to assess it. Strong correlations were demonstrated in students (n = 466) between lower-level dimensions, independent of the assessment method. Disintegration lay beyond the Five-Factor Model (FFM) space. This finding was replicated across informant types (self, mother, and father), samples (students and a national representative sample, n = 1001), and units of analyses (facets and items). The most frequent approach to preserve the FFM taxonomy of both normal and non-normal personality variants - mapping psychotic-like phenomena onto the Openness domain - found little support in our data. Disintegration was normally distributed in the general population.",
publisher = "Academic Press Inc Elsevier Science, San Diego",
journal = "Journal of Research in Personality",
title = "Disintegration: A reconceptualization of psychosis proneness as a personality trait separate from the Big Five",
pages = "201-187",
volume = "70",
doi = "10.1016/j.jrp.2017.06.001"
}
Knežević, G., Savić, D., Kutlešić, V.,& Opačić, G.. (2017). Disintegration: A reconceptualization of psychosis proneness as a personality trait separate from the Big Five. in Journal of Research in Personality
Academic Press Inc Elsevier Science, San Diego., 70, 187-201.
https://doi.org/10.1016/j.jrp.2017.06.001
Knežević G, Savić D, Kutlešić V, Opačić G. Disintegration: A reconceptualization of psychosis proneness as a personality trait separate from the Big Five. in Journal of Research in Personality. 2017;70:187-201.
doi:10.1016/j.jrp.2017.06.001 .
Knežević, Goran, Savić, Danka, Kutlešić, Vesna, Opačić, Goran, "Disintegration: A reconceptualization of psychosis proneness as a personality trait separate from the Big Five" in Journal of Research in Personality, 70 (2017):187-201,
https://doi.org/10.1016/j.jrp.2017.06.001 . .
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38

Posttraumatic and depressive symptoms in beta-endorphin dynamics

Savić, Danka; Knežević, Goran; Matić, Gordana; Damjanović, Svetozar; Spirić, Željko

(Elsevier Science BV, Amsterdam, 2015)

TY  - JOUR
AU  - Savić, Danka
AU  - Knežević, Goran
AU  - Matić, Gordana
AU  - Damjanović, Svetozar
AU  - Spirić, Željko
PY  - 2015
UR  - http://reff.f.bg.ac.rs/handle/123456789/1961
AB  - A disturbed beta-endorphin system can be a part of the post-traumatic stress disorder (PTSD) and depression allostasis. Study subjects (N=392) included those with PTSD and/or (stress-induced) depression, and healthy controls with and without traumas. The aim of the study was to examine the network of relations centered around plasma beta-endorphin. The network included anxiety (as a personality trait), traumatic events, pain, aggressiveness, depressive symptoms, and three clusters of PTSD symptoms: intrusions, avoidance, and hyperarousal. Beta-endorphin was represented by individual mean from 13 time points (BEmean), reflecting the total amount of the peripherally secreted hormone, and the coefficient of variation (BEvar), calculated as the ratio of standard deviation to the mean, reflecting the hormone's dynamics. BEvar correlated with all other variables, BEmean had no correlations. Structural equation modeling (SEM) was used to examine all interrelations (including their directions) of BEvar and the state/trait variables in the context of their entirety. The model revealed that hyperarousal and anxiety were the only direct agents of peripheral beta-endorphin fluctuations, mediating the effects of other variables. Traumatic events and intrusions act on BEvar via hyperarousal, while depressive symptoms, avoidance, and pain act via anxiety. Hyperarousal should be emphasized as the main agent not only because its effect on BEvar is larger than that of anxiety, but also because it increases anxiety itself (via avoidance and pain). All influences on BEvar are positive and they indicate long-term (sensitizing) effects (as opposed to direct stimulation, for example, by acute pain, anger, etc.). Relations apart from beta-endorphin are also discussed.
PB  - Elsevier Science BV, Amsterdam
T2  - Journal of Affective Disorders
T1  - Posttraumatic and depressive symptoms in beta-endorphin dynamics
EP  - 66
SP  - 61
VL  - 181
DO  - 10.1016/j.jad.2015.03.063
ER  - 
@article{
author = "Savić, Danka and Knežević, Goran and Matić, Gordana and Damjanović, Svetozar and Spirić, Željko",
year = "2015",
abstract = "A disturbed beta-endorphin system can be a part of the post-traumatic stress disorder (PTSD) and depression allostasis. Study subjects (N=392) included those with PTSD and/or (stress-induced) depression, and healthy controls with and without traumas. The aim of the study was to examine the network of relations centered around plasma beta-endorphin. The network included anxiety (as a personality trait), traumatic events, pain, aggressiveness, depressive symptoms, and three clusters of PTSD symptoms: intrusions, avoidance, and hyperarousal. Beta-endorphin was represented by individual mean from 13 time points (BEmean), reflecting the total amount of the peripherally secreted hormone, and the coefficient of variation (BEvar), calculated as the ratio of standard deviation to the mean, reflecting the hormone's dynamics. BEvar correlated with all other variables, BEmean had no correlations. Structural equation modeling (SEM) was used to examine all interrelations (including their directions) of BEvar and the state/trait variables in the context of their entirety. The model revealed that hyperarousal and anxiety were the only direct agents of peripheral beta-endorphin fluctuations, mediating the effects of other variables. Traumatic events and intrusions act on BEvar via hyperarousal, while depressive symptoms, avoidance, and pain act via anxiety. Hyperarousal should be emphasized as the main agent not only because its effect on BEvar is larger than that of anxiety, but also because it increases anxiety itself (via avoidance and pain). All influences on BEvar are positive and they indicate long-term (sensitizing) effects (as opposed to direct stimulation, for example, by acute pain, anger, etc.). Relations apart from beta-endorphin are also discussed.",
publisher = "Elsevier Science BV, Amsterdam",
journal = "Journal of Affective Disorders",
title = "Posttraumatic and depressive symptoms in beta-endorphin dynamics",
pages = "66-61",
volume = "181",
doi = "10.1016/j.jad.2015.03.063"
}
Savić, D., Knežević, G., Matić, G., Damjanović, S.,& Spirić, Ž.. (2015). Posttraumatic and depressive symptoms in beta-endorphin dynamics. in Journal of Affective Disorders
Elsevier Science BV, Amsterdam., 181, 61-66.
https://doi.org/10.1016/j.jad.2015.03.063
Savić D, Knežević G, Matić G, Damjanović S, Spirić Ž. Posttraumatic and depressive symptoms in beta-endorphin dynamics. in Journal of Affective Disorders. 2015;181:61-66.
doi:10.1016/j.jad.2015.03.063 .
Savić, Danka, Knežević, Goran, Matić, Gordana, Damjanović, Svetozar, Spirić, Željko, "Posttraumatic and depressive symptoms in beta-endorphin dynamics" in Journal of Affective Disorders, 181 (2015):61-66,
https://doi.org/10.1016/j.jad.2015.03.063 . .
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GR gene BclI polymorphysm changes the path, but not the level, of dexamethasone-induced cortisol suppression

Savić, Danka; Knežević, Goran; Damjanović, Svetozar; Antić, Jadranka; Matić, Gordana

(Elsevier Science BV, Amsterdam, 2014)

TY  - JOUR
AU  - Savić, Danka
AU  - Knežević, Goran
AU  - Damjanović, Svetozar
AU  - Antić, Jadranka
AU  - Matić, Gordana
PY  - 2014
UR  - http://reff.f.bg.ac.rs/handle/123456789/1812
AB  - Background: The hypothalamo-pituitary-adrenocortical (HPA) axis self-regulation is achieved via cortisol binding to mineralocorticoid (MR) and glucocorticoid receptors (GR). It is often disturbed in mental disorders, particularly in those where traumatic stress has been implicated, such as posttraumatic stress disorder and depression. Although dexamethasone suppression test (DST) is often used as diagnostic aid, the findings still vary. In search of the factors influencing the DST outcome, we examined the glucocorticoicl receptor (GR) gene Bell polymorphism. Methods: A total of 229 male subjects were classified into three Bell groups: two groups with homozygous carriers (of the G allele, N=108, and of the C allele, N=26), and one with heterozygous carriers (N=95). Multiple hierarchical linear regression analysis was clone, where the dependent variable was the clexamethasone-inclucecl cortisol suppression, and predictors included receptor variables. The interactions of the count of 'G's with the predictors were introduced to single out the effects of the G allele. Results: The means of all studied variables, including suppression, are statistically the same in the three groups. However, the mechanism of suppression involves MRs only in the G allele carriers. Limitations: The subjects were selected by criteria suited for the aim of the large project whose part is this study, hence the relatively small number of CC carriers. Also, we did not assess MR functional properties that would probably sharpen the results. Conclusion: Our finding that MRs participate in cortisol suppression in the G allele carriers suggests that research aimed at refining HPA axis-based therapy might require its adjustment for such patients.,
PB  - Elsevier Science BV, Amsterdam
T2  - Journal of Affective Disorders
T1  - GR gene BclI polymorphysm changes the path, but not the level, of dexamethasone-induced cortisol suppression
EP  - 4
SP  - 1
VL  - 168
DO  - 10.1016/j.jad.2014.06.046
ER  - 
@article{
author = "Savić, Danka and Knežević, Goran and Damjanović, Svetozar and Antić, Jadranka and Matić, Gordana",
year = "2014",
abstract = "Background: The hypothalamo-pituitary-adrenocortical (HPA) axis self-regulation is achieved via cortisol binding to mineralocorticoid (MR) and glucocorticoid receptors (GR). It is often disturbed in mental disorders, particularly in those where traumatic stress has been implicated, such as posttraumatic stress disorder and depression. Although dexamethasone suppression test (DST) is often used as diagnostic aid, the findings still vary. In search of the factors influencing the DST outcome, we examined the glucocorticoicl receptor (GR) gene Bell polymorphism. Methods: A total of 229 male subjects were classified into three Bell groups: two groups with homozygous carriers (of the G allele, N=108, and of the C allele, N=26), and one with heterozygous carriers (N=95). Multiple hierarchical linear regression analysis was clone, where the dependent variable was the clexamethasone-inclucecl cortisol suppression, and predictors included receptor variables. The interactions of the count of 'G's with the predictors were introduced to single out the effects of the G allele. Results: The means of all studied variables, including suppression, are statistically the same in the three groups. However, the mechanism of suppression involves MRs only in the G allele carriers. Limitations: The subjects were selected by criteria suited for the aim of the large project whose part is this study, hence the relatively small number of CC carriers. Also, we did not assess MR functional properties that would probably sharpen the results. Conclusion: Our finding that MRs participate in cortisol suppression in the G allele carriers suggests that research aimed at refining HPA axis-based therapy might require its adjustment for such patients.,",
publisher = "Elsevier Science BV, Amsterdam",
journal = "Journal of Affective Disorders",
title = "GR gene BclI polymorphysm changes the path, but not the level, of dexamethasone-induced cortisol suppression",
pages = "4-1",
volume = "168",
doi = "10.1016/j.jad.2014.06.046"
}
Savić, D., Knežević, G., Damjanović, S., Antić, J.,& Matić, G.. (2014). GR gene BclI polymorphysm changes the path, but not the level, of dexamethasone-induced cortisol suppression. in Journal of Affective Disorders
Elsevier Science BV, Amsterdam., 168, 1-4.
https://doi.org/10.1016/j.jad.2014.06.046
Savić D, Knežević G, Damjanović S, Antić J, Matić G. GR gene BclI polymorphysm changes the path, but not the level, of dexamethasone-induced cortisol suppression. in Journal of Affective Disorders. 2014;168:1-4.
doi:10.1016/j.jad.2014.06.046 .
Savić, Danka, Knežević, Goran, Damjanović, Svetozar, Antić, Jadranka, Matić, Gordana, "GR gene BclI polymorphysm changes the path, but not the level, of dexamethasone-induced cortisol suppression" in Journal of Affective Disorders, 168 (2014):1-4,
https://doi.org/10.1016/j.jad.2014.06.046 . .
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5

Mineralocorticoid receptor and heat shock protein expression levels in peripheral lymphocytes from war trauma-exposed men with and without PTSD

Matić, Gordana; Vojnović-Milutinović, Danijela; Nestorov, Jelena; Elaković, Ivana; Manitašević-Jovanović, Sanja; Elzaedi, Younis Mouftah; Perišić, Tatjana; Dunderski, Jadranka; Damjanović, Svetozar; Knežević, Goran; Spirić, Željko; Vermetten, Eric; Savić, Danka

(Elsevier Ireland Ltd, Clare, 2014)

TY  - JOUR
AU  - Matić, Gordana
AU  - Vojnović-Milutinović, Danijela
AU  - Nestorov, Jelena
AU  - Elaković, Ivana
AU  - Manitašević-Jovanović, Sanja
AU  - Elzaedi, Younis Mouftah
AU  - Perišić, Tatjana
AU  - Dunderski, Jadranka
AU  - Damjanović, Svetozar
AU  - Knežević, Goran
AU  - Spirić, Željko
AU  - Vermetten, Eric
AU  - Savić, Danka
PY  - 2014
UR  - http://reff.f.bg.ac.rs/handle/123456789/1796
AB  - Alterations in the number and functional status of mineralocorticoid (MR) and glucocorticoid receptors (GR) may contribute to vulnerability to posttraumatic stress disorder (PTSD). Corticosteroid receptors are chaperoned by heat shock proteins Hsp90 and Hsp70. We examined relations between corticosteroid receptor and heat shock protein expression levels, and related them with war trauma exposure, PTSD and resilience to PTSD. Relative levels of MR. Hsp90 and Hsp70 were determined by immunoblotting in lymphocytes from war trauma-exposed men with current PTSD (current PTSD group, n=113), with lifetime PTSD (life-time PTSD group, n=61) and without PTSD (trauma control group, n=88), and from non-traumatized healthy controls (healthy control group, n=85). Between-group differences in MR, Hsp90 and Hsp70 levels and in MR/GR ratio were not observed. The level of MR was correlated with both Hsp90 and Hsp70 levels in trauma control and healthy control groups. On the other hand, GR level was correlated only with Hsp90 level, and this correlation was evident in current PTSD and trauma control groups. In conclusion, PTSD and exposure to trauma are not related to changes in lymphocyte MR, Hsp90 or Hsp70 levels, but may be associated with disturbances in corticosteroid receptors interaction with heat shock proteins.
PB  - Elsevier Ireland Ltd, Clare
T2  - Psychiatry Research
T1  - Mineralocorticoid receptor and heat shock protein expression levels in peripheral lymphocytes from war trauma-exposed men with and without PTSD
EP  - 385
IS  - 2
SP  - 379
VL  - 215
DO  - 10.1016/j.psychres.2013.11.022
ER  - 
@article{
author = "Matić, Gordana and Vojnović-Milutinović, Danijela and Nestorov, Jelena and Elaković, Ivana and Manitašević-Jovanović, Sanja and Elzaedi, Younis Mouftah and Perišić, Tatjana and Dunderski, Jadranka and Damjanović, Svetozar and Knežević, Goran and Spirić, Željko and Vermetten, Eric and Savić, Danka",
year = "2014",
abstract = "Alterations in the number and functional status of mineralocorticoid (MR) and glucocorticoid receptors (GR) may contribute to vulnerability to posttraumatic stress disorder (PTSD). Corticosteroid receptors are chaperoned by heat shock proteins Hsp90 and Hsp70. We examined relations between corticosteroid receptor and heat shock protein expression levels, and related them with war trauma exposure, PTSD and resilience to PTSD. Relative levels of MR. Hsp90 and Hsp70 were determined by immunoblotting in lymphocytes from war trauma-exposed men with current PTSD (current PTSD group, n=113), with lifetime PTSD (life-time PTSD group, n=61) and without PTSD (trauma control group, n=88), and from non-traumatized healthy controls (healthy control group, n=85). Between-group differences in MR, Hsp90 and Hsp70 levels and in MR/GR ratio were not observed. The level of MR was correlated with both Hsp90 and Hsp70 levels in trauma control and healthy control groups. On the other hand, GR level was correlated only with Hsp90 level, and this correlation was evident in current PTSD and trauma control groups. In conclusion, PTSD and exposure to trauma are not related to changes in lymphocyte MR, Hsp90 or Hsp70 levels, but may be associated with disturbances in corticosteroid receptors interaction with heat shock proteins.",
publisher = "Elsevier Ireland Ltd, Clare",
journal = "Psychiatry Research",
title = "Mineralocorticoid receptor and heat shock protein expression levels in peripheral lymphocytes from war trauma-exposed men with and without PTSD",
pages = "385-379",
number = "2",
volume = "215",
doi = "10.1016/j.psychres.2013.11.022"
}
Matić, G., Vojnović-Milutinović, D., Nestorov, J., Elaković, I., Manitašević-Jovanović, S., Elzaedi, Y. M., Perišić, T., Dunderski, J., Damjanović, S., Knežević, G., Spirić, Ž., Vermetten, E.,& Savić, D.. (2014). Mineralocorticoid receptor and heat shock protein expression levels in peripheral lymphocytes from war trauma-exposed men with and without PTSD. in Psychiatry Research
Elsevier Ireland Ltd, Clare., 215(2), 379-385.
https://doi.org/10.1016/j.psychres.2013.11.022
Matić G, Vojnović-Milutinović D, Nestorov J, Elaković I, Manitašević-Jovanović S, Elzaedi YM, Perišić T, Dunderski J, Damjanović S, Knežević G, Spirić Ž, Vermetten E, Savić D. Mineralocorticoid receptor and heat shock protein expression levels in peripheral lymphocytes from war trauma-exposed men with and without PTSD. in Psychiatry Research. 2014;215(2):379-385.
doi:10.1016/j.psychres.2013.11.022 .
Matić, Gordana, Vojnović-Milutinović, Danijela, Nestorov, Jelena, Elaković, Ivana, Manitašević-Jovanović, Sanja, Elzaedi, Younis Mouftah, Perišić, Tatjana, Dunderski, Jadranka, Damjanović, Svetozar, Knežević, Goran, Spirić, Željko, Vermetten, Eric, Savić, Danka, "Mineralocorticoid receptor and heat shock protein expression levels in peripheral lymphocytes from war trauma-exposed men with and without PTSD" in Psychiatry Research, 215, no. 2 (2014):379-385,
https://doi.org/10.1016/j.psychres.2013.11.022 . .
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Lymphocyte glucocorticoid receptor expression level and hormone-binding properties differ between war trauma-exposed men with and without PTSD

Matić, Gordana; Vojnović-Milutinović, Danijela; Nestorov, Jelena; Elaković, Ivana; Manitašević-Jovanović, Sanja; Perišić, Tatjana; Dunderski, Jadranka; Damjanović, Svetozar; Knežević, Goran; Spirić, Željko; Vermetten, Eric; Savić, Danka

(Pergamon-Elsevier Science Ltd, Oxford, 2013)

TY  - JOUR
AU  - Matić, Gordana
AU  - Vojnović-Milutinović, Danijela
AU  - Nestorov, Jelena
AU  - Elaković, Ivana
AU  - Manitašević-Jovanović, Sanja
AU  - Perišić, Tatjana
AU  - Dunderski, Jadranka
AU  - Damjanović, Svetozar
AU  - Knežević, Goran
AU  - Spirić, Željko
AU  - Vermetten, Eric
AU  - Savić, Danka
PY  - 2013
UR  - http://reff.f.bg.ac.rs/handle/123456789/1626
AB  - Objective: Posttraumatic stress disorder (PTSD) has been shown to be associated with altered glucocorticoid receptor (GR) activity. We studied the expression and functional properties of the receptor in peripheral blood mononuclear cells (PBMCs) from non-traumatized healthy individuals (healthy controls; n = 85), and war trauma-exposed individuals with current PTSD (n = 113), with life-time PTSD (n = 61) and without PTSD (trauma controls; n = 88). The aim of the study was to distinguish the receptor alterations related to PTSD from those related to trauma itself or to resilience to PTSD. Methods: Functional status of the receptor was assessed by radioligand binding and lysozyme synthesis inhibition assays. The level of GR gene expression was measured by quantitative PCR and immunoblotting. Results: Current PTSD patients had the lowest, while trauma controls had the highest number of glucocorticoid binding sites (B-max) in PBMCs. Hormone-binding potential (B-max/K-D ratio) of the receptor was diminished in the current PTSD group in comparison to all other study groups. Correlation between B-max and K-D that normally exists in healthy individuals was decreased in the current PTSD group. Contrasting B-max data, GR protein level was lower in trauma controls than in participants with current or life-time PTSD. Conclusions: Current PTSD is characterized by reduced lymphocyte GR hormone-binding potential and by disturbed compensation between B-max and hormone-binding affinity. Resilience to PTSD is associated with enlarged fraction of the receptor molecules capable of hormone binding, within the total receptor molecule population in PBMCs.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Progress in Neuro-Psychopharmacology & Biological Psychiatry
T1  - Lymphocyte glucocorticoid receptor expression level and hormone-binding properties differ between war trauma-exposed men with and without PTSD
EP  - 245
SP  - 238
VL  - 43
DO  - 10.1016/j.pnpbp.2013.01.005
ER  - 
@article{
author = "Matić, Gordana and Vojnović-Milutinović, Danijela and Nestorov, Jelena and Elaković, Ivana and Manitašević-Jovanović, Sanja and Perišić, Tatjana and Dunderski, Jadranka and Damjanović, Svetozar and Knežević, Goran and Spirić, Željko and Vermetten, Eric and Savić, Danka",
year = "2013",
abstract = "Objective: Posttraumatic stress disorder (PTSD) has been shown to be associated with altered glucocorticoid receptor (GR) activity. We studied the expression and functional properties of the receptor in peripheral blood mononuclear cells (PBMCs) from non-traumatized healthy individuals (healthy controls; n = 85), and war trauma-exposed individuals with current PTSD (n = 113), with life-time PTSD (n = 61) and without PTSD (trauma controls; n = 88). The aim of the study was to distinguish the receptor alterations related to PTSD from those related to trauma itself or to resilience to PTSD. Methods: Functional status of the receptor was assessed by radioligand binding and lysozyme synthesis inhibition assays. The level of GR gene expression was measured by quantitative PCR and immunoblotting. Results: Current PTSD patients had the lowest, while trauma controls had the highest number of glucocorticoid binding sites (B-max) in PBMCs. Hormone-binding potential (B-max/K-D ratio) of the receptor was diminished in the current PTSD group in comparison to all other study groups. Correlation between B-max and K-D that normally exists in healthy individuals was decreased in the current PTSD group. Contrasting B-max data, GR protein level was lower in trauma controls than in participants with current or life-time PTSD. Conclusions: Current PTSD is characterized by reduced lymphocyte GR hormone-binding potential and by disturbed compensation between B-max and hormone-binding affinity. Resilience to PTSD is associated with enlarged fraction of the receptor molecules capable of hormone binding, within the total receptor molecule population in PBMCs.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Progress in Neuro-Psychopharmacology & Biological Psychiatry",
title = "Lymphocyte glucocorticoid receptor expression level and hormone-binding properties differ between war trauma-exposed men with and without PTSD",
pages = "245-238",
volume = "43",
doi = "10.1016/j.pnpbp.2013.01.005"
}
Matić, G., Vojnović-Milutinović, D., Nestorov, J., Elaković, I., Manitašević-Jovanović, S., Perišić, T., Dunderski, J., Damjanović, S., Knežević, G., Spirić, Ž., Vermetten, E.,& Savić, D.. (2013). Lymphocyte glucocorticoid receptor expression level and hormone-binding properties differ between war trauma-exposed men with and without PTSD. in Progress in Neuro-Psychopharmacology & Biological Psychiatry
Pergamon-Elsevier Science Ltd, Oxford., 43, 238-245.
https://doi.org/10.1016/j.pnpbp.2013.01.005
Matić G, Vojnović-Milutinović D, Nestorov J, Elaković I, Manitašević-Jovanović S, Perišić T, Dunderski J, Damjanović S, Knežević G, Spirić Ž, Vermetten E, Savić D. Lymphocyte glucocorticoid receptor expression level and hormone-binding properties differ between war trauma-exposed men with and without PTSD. in Progress in Neuro-Psychopharmacology & Biological Psychiatry. 2013;43:238-245.
doi:10.1016/j.pnpbp.2013.01.005 .
Matić, Gordana, Vojnović-Milutinović, Danijela, Nestorov, Jelena, Elaković, Ivana, Manitašević-Jovanović, Sanja, Perišić, Tatjana, Dunderski, Jadranka, Damjanović, Svetozar, Knežević, Goran, Spirić, Željko, Vermetten, Eric, Savić, Danka, "Lymphocyte glucocorticoid receptor expression level and hormone-binding properties differ between war trauma-exposed men with and without PTSD" in Progress in Neuro-Psychopharmacology & Biological Psychiatry, 43 (2013):238-245,
https://doi.org/10.1016/j.pnpbp.2013.01.005 . .
41
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The role of personality and traumatic events in cortisol levels - Where does PTSD fit in?

Savić, Danka; Knežević, Goran; Damjanović, Svetozar; Spirić, Željko; Matić, Gordana

(Pergamon-Elsevier Science Ltd, Oxford, 2012)

TY  - JOUR
AU  - Savić, Danka
AU  - Knežević, Goran
AU  - Damjanović, Svetozar
AU  - Spirić, Željko
AU  - Matić, Gordana
PY  - 2012
UR  - http://reff.f.bg.ac.rs/handle/123456789/1362
AB  - Background: Studies of cortisol in post-traumatic stress disorder (PTSD) have yielded mixed results. We hypothesize that personality traits and traumatic experiences could be the confounders of cortisol measures and disease symptoms. Method: This study was a part of a broader project in which simultaneous psychological and biological investigations were carried out in hospital conditions on 400 male participants categorized by four groups: (A) 133 with current PTSD, (B) 66 with lifetime PTSD, (C) 102 trauma controls, and (D) 99 healthy controls (matched by age and education). Cortisol and ACTH were measured in blood samples taken hourly from 22:00 h to 09:00 h, with an additional sample at 07:30 h (resting state and morning rise). The next night, dexamethasone (0.5 mg) suppression test was performed. Results: No significant differences in basal cortisol and ACTH were found between study groups. The trait Conscientiousness, negatively modulated by Extraversion (assessed by NEO Personality Inventory-Revised) was found to correlate with cortisol (but not with ACTH). Group differences are found on suppression. Structural equation modeling shows excellent fit only when the paths (influences) from Conscientiousness to basal cortisol and from traumatic events to suppression are present. The paths connecting suppression and PTSD symptoms do not contribute. Conclusions: Two sources of differences of hypothalamo-pituitary-adrenocortical axis functioning are implied, both only indirectly connected to PTSD. It seems that basal cortisol secretion is associated more tightly with personality (introvertively modulated Conscientiousness), while the regulation by glucocorticoid receptor system is sensitized by repeated traumatic situations.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Psychoneuroendocrinology
T1  - The role of personality and traumatic events in cortisol levels - Where does PTSD fit in?
EP  - 947
IS  - 7
SP  - 937
VL  - 37
DO  - 10.1016/j.psyneuen.2011.11.001
ER  - 
@article{
author = "Savić, Danka and Knežević, Goran and Damjanović, Svetozar and Spirić, Željko and Matić, Gordana",
year = "2012",
abstract = "Background: Studies of cortisol in post-traumatic stress disorder (PTSD) have yielded mixed results. We hypothesize that personality traits and traumatic experiences could be the confounders of cortisol measures and disease symptoms. Method: This study was a part of a broader project in which simultaneous psychological and biological investigations were carried out in hospital conditions on 400 male participants categorized by four groups: (A) 133 with current PTSD, (B) 66 with lifetime PTSD, (C) 102 trauma controls, and (D) 99 healthy controls (matched by age and education). Cortisol and ACTH were measured in blood samples taken hourly from 22:00 h to 09:00 h, with an additional sample at 07:30 h (resting state and morning rise). The next night, dexamethasone (0.5 mg) suppression test was performed. Results: No significant differences in basal cortisol and ACTH were found between study groups. The trait Conscientiousness, negatively modulated by Extraversion (assessed by NEO Personality Inventory-Revised) was found to correlate with cortisol (but not with ACTH). Group differences are found on suppression. Structural equation modeling shows excellent fit only when the paths (influences) from Conscientiousness to basal cortisol and from traumatic events to suppression are present. The paths connecting suppression and PTSD symptoms do not contribute. Conclusions: Two sources of differences of hypothalamo-pituitary-adrenocortical axis functioning are implied, both only indirectly connected to PTSD. It seems that basal cortisol secretion is associated more tightly with personality (introvertively modulated Conscientiousness), while the regulation by glucocorticoid receptor system is sensitized by repeated traumatic situations.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Psychoneuroendocrinology",
title = "The role of personality and traumatic events in cortisol levels - Where does PTSD fit in?",
pages = "947-937",
number = "7",
volume = "37",
doi = "10.1016/j.psyneuen.2011.11.001"
}
Savić, D., Knežević, G., Damjanović, S., Spirić, Ž.,& Matić, G.. (2012). The role of personality and traumatic events in cortisol levels - Where does PTSD fit in?. in Psychoneuroendocrinology
Pergamon-Elsevier Science Ltd, Oxford., 37(7), 937-947.
https://doi.org/10.1016/j.psyneuen.2011.11.001
Savić D, Knežević G, Damjanović S, Spirić Ž, Matić G. The role of personality and traumatic events in cortisol levels - Where does PTSD fit in?. in Psychoneuroendocrinology. 2012;37(7):937-947.
doi:10.1016/j.psyneuen.2011.11.001 .
Savić, Danka, Knežević, Goran, Damjanović, Svetozar, Spirić, Željko, Matić, Gordana, "The role of personality and traumatic events in cortisol levels - Where does PTSD fit in?" in Psychoneuroendocrinology, 37, no. 7 (2012):937-947,
https://doi.org/10.1016/j.psyneuen.2011.11.001 . .
1
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22

Is there a biological difference between trauma-related depression and PTSD? DST says 'NO'

Savić, Danka; Knežević, Goran; Damjanović, Svetozar; Spirić, Željko; Matić, Gordana

(Pergamon-Elsevier Science Ltd, Oxford, 2012)

TY  - JOUR
AU  - Savić, Danka
AU  - Knežević, Goran
AU  - Damjanović, Svetozar
AU  - Spirić, Željko
AU  - Matić, Gordana
PY  - 2012
UR  - http://reff.f.bg.ac.rs/handle/123456789/1338
AB  - The use of the low-dose dexamethasone suppression test (DST) as a potentially discriminative marker between post-traumatic stress disorder (PTSD) and depression is still under discussion. In order to compare the influence of these psychopathologies on the DST results, we examined suppression in war-traumatized subjects with one or both of these disorders, as well as in healthy controls. Based on our previous findings, we hypothesized that subjects with any disorder would exhibit higher dexamethasone suppression than healthy controls due to traumatic experiences. This study was a part of a broader project in which simultaneous psychological and biological investigations were carried out in hospital conditions on 399 mate participants: 57 with PTSD, 28 with depression, 76 with PTSD + depression, and 238 healthy controls. Cortisol was measured in blood samples taken at 0900 h before and after administering 0.5 mg of dexamethasone (at 2300 h). Group means standard deviation of cortisol suppression were: 79.4 +/- 18.5 in the PTSD group, 80.8 +/- 11.6 in the depression group, 77.5 +/- 24.6 in the group with PTSD+depression, and 66.8 +/- 34.6 in healthy controls. The first three groups suppressed significantly more than the fourth. When the number of traumas was introduced as a covariate, the differences disappeared. The hypothesis was confirmed: in respect to DST, the examined trauma-related psychopathologies showed the same pattern: hypersuppression, due to multiple traumatic experiences.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Psychoneuroendocrinology
T1  - Is there a biological difference between trauma-related depression and PTSD? DST says 'NO'
EP  - 1520
IS  - 9
SP  - 1516
VL  - 37
DO  - 10.1016/j.psyneuen.2012.02.005
ER  - 
@article{
author = "Savić, Danka and Knežević, Goran and Damjanović, Svetozar and Spirić, Željko and Matić, Gordana",
year = "2012",
abstract = "The use of the low-dose dexamethasone suppression test (DST) as a potentially discriminative marker between post-traumatic stress disorder (PTSD) and depression is still under discussion. In order to compare the influence of these psychopathologies on the DST results, we examined suppression in war-traumatized subjects with one or both of these disorders, as well as in healthy controls. Based on our previous findings, we hypothesized that subjects with any disorder would exhibit higher dexamethasone suppression than healthy controls due to traumatic experiences. This study was a part of a broader project in which simultaneous psychological and biological investigations were carried out in hospital conditions on 399 mate participants: 57 with PTSD, 28 with depression, 76 with PTSD + depression, and 238 healthy controls. Cortisol was measured in blood samples taken at 0900 h before and after administering 0.5 mg of dexamethasone (at 2300 h). Group means standard deviation of cortisol suppression were: 79.4 +/- 18.5 in the PTSD group, 80.8 +/- 11.6 in the depression group, 77.5 +/- 24.6 in the group with PTSD+depression, and 66.8 +/- 34.6 in healthy controls. The first three groups suppressed significantly more than the fourth. When the number of traumas was introduced as a covariate, the differences disappeared. The hypothesis was confirmed: in respect to DST, the examined trauma-related psychopathologies showed the same pattern: hypersuppression, due to multiple traumatic experiences.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Psychoneuroendocrinology",
title = "Is there a biological difference between trauma-related depression and PTSD? DST says 'NO'",
pages = "1520-1516",
number = "9",
volume = "37",
doi = "10.1016/j.psyneuen.2012.02.005"
}
Savić, D., Knežević, G., Damjanović, S., Spirić, Ž.,& Matić, G.. (2012). Is there a biological difference between trauma-related depression and PTSD? DST says 'NO'. in Psychoneuroendocrinology
Pergamon-Elsevier Science Ltd, Oxford., 37(9), 1516-1520.
https://doi.org/10.1016/j.psyneuen.2012.02.005
Savić D, Knežević G, Damjanović S, Spirić Ž, Matić G. Is there a biological difference between trauma-related depression and PTSD? DST says 'NO'. in Psychoneuroendocrinology. 2012;37(9):1516-1520.
doi:10.1016/j.psyneuen.2012.02.005 .
Savić, Danka, Knežević, Goran, Damjanović, Svetozar, Spirić, Željko, Matić, Gordana, "Is there a biological difference between trauma-related depression and PTSD? DST says 'NO'" in Psychoneuroendocrinology, 37, no. 9 (2012):1516-1520,
https://doi.org/10.1016/j.psyneuen.2012.02.005 . .
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