Literature DB >> 31687446

Data for "Social-evaluative threat: Stress response stages and influences of biological sex and neuroticism".

Eefje S Poppelaars1, Johannes Klackl1, Belinda Pletzer1, Frank H Wilhelm1, Eva Jonas1.   

Abstract

This Data In Brief article contains supplementary materials to the article "Social-evaluative threat: stress response stages and influences of biological sex and neuroticism" [1], and describes analysis results of an open dataset [2]. Additional information is provided regarding the methods, particularly: the analysis of individual stress response peak times per stress system, and the statistical analysis. Importantly, correlation tables are presented between the different stress systems, both for baseline stress levels as well as for stress responses, and significant associations are displayed in scatter plots.
© 2019 The Author(s).

Entities:  

Keywords:  Anxiety; Cortisol; Gender; Social-evaluative threat

Year:  2019        PMID: 31687446      PMCID: PMC6820083          DOI: 10.1016/j.dib.2019.104645

Source DB:  PubMed          Journal:  Data Brief        ISSN: 2352-3409


Specifications Table The correlation coefficients could be used in a meta-analysis about associations between stress responses. The information about the timing of individual stress responses in different systems and their sex differences could inform research on the timing of stress response. Our approach to missing data management ‒ particularly the use of multiple imputation ‒ can serve to inspire other researchers on how to manage missing data.

Experimental design, materials, and methods

Full descriptions of the experimental design, materials, and methods can be found at the primary article [1].

Social-evaluative threat (SET) manipulation

Social-evaluative threat was induced using a public speaking task. Fig. 1 shows a screenshot of the video audience (with permission).
Fig. 1

Screenshot of video audience and the timer (lower right corner).

Screenshot of video audience and the timer (lower right corner).

Assessments and measures

Traits

We used self-report questionnaires to measure extraversion and neuroticism (Big Five Aspects Scale using twenty items each) [3], as well as related traits such as: BIS-BAS sensitivity (behavioral inhibition and approach scales; using seven items for BIS and twelve items for BAS) [4], social anxiety (Liebowitz Social Anxiety Scale; using 48 items) [5], self-esteem (Rosenberg Self-Esteem Scale; using ten items) [6], need to belong (Need to Belong scale; using ten items) [7,8], rumination (Post-event Rumination Questionnaire; using eight items for positive rumination (excl. items #4, 12, 20) and thirteen items for negative rumination (excl. items #5, 7, 15)) [9,10], and masculinity and femininity (Multifaceted Gender-Related Attributes Survey; using three items each) [11]. Additionally, English language competence (Cambridge online test using 25 items; www.cambridgeenglish.org/test-your-english/general-english/) was measured as a confounding variable. Based on relevance in the literature and our hypotheses, only the extraversion and neuroticism traits were selected to be featured in the regression models and in the primary article.

Self-reported appraisals

Resource and demand appraisals (stage one of the stress response [12]) were both assessed with single questions. Demand appraisal was measured with: “How demanding do you expect the upcoming task to be?” and resource appraisal with: “How able are you to cope with the upcoming task?”. A continuous composite measure of resources and demands was calculated, by subtracting demands from resources, yielding positive values in case of higher resources than demands (challenge) and negative values in case of higher demands than re-sources (threat).

Cardiovascular physiology

Cardiovascular physiology was recorded to measure the following indices of stage two of the stress response: heart rate (HR), mean blood pressure (BP), pre-ejection period (PEP), and respiratory sinus arrhythmia (RSA), as well as respiratory rate (RR) as a covariate in RSA analyses [13]. Electrocardiography (ECG), impedance cardiography (ICG), and respiration were recorded continuously, while systolic and diastolic BP was measured repeatedly. The ECG and ICG signals were analyzed using ANSLAB [14], according to standard analysis protocols. Mean blood pressure was calculated using the formula: 2/3 diastolic +1/3 systolic [16]. Additional information is provided for ICG measures that were not discussed in the primary article but are included in the open dataset: cardiac output, total peripheral resistance, and threat-challenge index. Cardiac output (CO in liters per minute) was calculated by multiplying heart rate with stroke volume (as estimated in ANSLAB [14] using the Kubicek formula [15]). Total peripheral resistance (TPR in dyne-seconds * cm−5) was computed by dividing mean blood pressure by CO and multiplying that value by 80 [17]. A threat-challenge index for each time point was calculated by subtracting z-transformed-values of TPR from CO [18,19]. Thus, higher values on the TCI indicate a stronger challenge motivational state whereas lower values on the TCI indicate a stronger threat motivational state.

Self-reported affective and motivational states

Affective and motivational responses (stage three of the stress response) were measured using state anxiety and state approach motivation, respectively [10,20,21]. State anxiety was measured with the single question: “How anxious do you feel right now?”, and state approach motivation was measured with the single question: “How much are you looking forward to the next part of the study?”.

Endocrine physiology

In order to assess free salivary cortisol (stage four of the stress response), seven saliva samples were collected throughout the experiment and frozen. Analysis was performed using ELISA (DeMediTec Diagnostics, Kiel, Germany) by using two duplicate measures for each saliva sample to increase reliability, and samples with intra-assay coefficients of variability above 25% were repeated.

Statistical analyses

Outlier detection

Outliers were detected based on significant values on the Grubbs test [22]. This statistic tests the deviation from the sample mean of the largest and smallest observation of a given variable. This test was applied over all variables (with Bonferroni-correction), and repeated until no significant outliers were present (i.e., after one round). Two outliers were excluded in these steps. Subsequently, the regression models using complete observations were tested for outliers in the Studentized residuals of each linear model (with Bonferroni-correction), based on the mean-shift outlier test [23]. One outlier was excluded in this step, resulting in three outlier participants in total.

Missing data management

A description of all missing observations and outliers per variable can be found in Table 1. Variables that did not contain any missing data or outliers are not included in Table 1 (Neuroticism, Extraversion, Resource-demand appraisal, State anxiety 1 through 4, ΔState anxiety, State approach motivation 1 through 4, ΔState approach motivation, Mean blood pressure 1 through 8, ΔMean blood pressure, Cortisol 2 through 7).
Table 1

Missing observations and outliers per variable.

VariableNumber of missing observationsNumber of outliers
State anxiety 570
State anxiety 670
State anxiety 770
State anxiety 870
State approach motivation 570
State approach motivation 670
State approach motivation 770
State approach motivation 870
HR 110
HR 210
HR 320
HR 431
HR 520
HR 620
HR 740
HR 840
ΔHR50
PEP 160
PEP 260
PEP 360
PEP 460
PEP 570
PEP 660
PEP 780
PEP 880
ΔPEP90
RSA 111
RSA 211
RSA 321
RSA 431
RSA 521
RSA 621
RSA 741
RSA 841
ΔRSA41
RR 150
RR 240
RR 330
RR 440
RR 530
RR 630
RR 750
RR 850
ΔRR70
Cortisol 101
ΔCortisol01

Note. HR = heart rate; PEP = pre-ejection period; RSA = respiratory sinus arrhythmia; RR = respiratory rate; Δ = individual reactivity.

Missing observations and outliers per variable. Note. HR = heart rate; PEP = pre-ejection period; RSA = respiratory sinus arrhythmia; RR = respiratory rate; Δ = individual reactivity.

Multiple imputation of missing data

Since twenty-four participants had some missing data points due to excessive noise, temporary sensor malfunction, or loose contacts, and another four participants had excluded outlier data points (see section Outlier detection), there were only thirty-eight complete observations in the dataset out of sixty-seven. To avoid the loss of 43.3% of our participants in the analyses, we multiply imputed the missing data using chained equations using the MICE package [24]; a “state of the art” missing data method. The imputation model did not contain all possible variables, considering the large number of variables in the dataset. Instead, only relevant variables were included for all variables to be imputed (as is recommended: Buuren and Groothuis-Oudshoorn, 2011): sex, age, trait extraversion, trait neuroticism, resource-demand appraisal, and all reactivity variables, as well as the other time points of the same measure; resulting in twenty to twenty-one predictors per variable. This is specified in the predictorMatrixAdj.xlsx file [2]. (For example, HR 1 was predicted by: sex, age, trait extraversion, trait neuroticism, resource-demand appraisal, reactivity variables of: state anxiety, state approach motivation, mean BP, PEP, RSA, RR, and cortisol, as well as the other HR time points: 2, 3, 4, 5, 6, 7, and 8.) Reactivity variables were passively imputed, based on a given formula to compute individual peak minus baseline (Δ; see SET reactivity section in primary article). Forty-four datasets were imputed, based on the rule of thumb that at least as many datasets need to be imputed as the percentage of incomplete cases [25]. Missing values were imputed by predictive mean matching, since in this method imputations are restricted to the observed values [24]. Two-hundred iterations were allowed to reach convergence. Plausibility of imputed variables was assessed by comparing them to complete observations using boxplots, strip plots, and density plots, and summary statistics. All subsequent analyses were performed for each of the imputed datasets and the resulting estimates were pooled according to Rubin's rules [26].

SET reactivity

SET responses were computed with a reactivity measure of individual peak minus baseline [27], henceforth identified as Δ. The peak represents the individual maximum or minimum value (depending on the measure) during or right after SET (i.e., either early or late anticipation, or early or late first recovery). Additionally, we calculated the area under the curve (AUC with respect to the increase [28]) for the cortisol response, which were strongly correlated, r = 0.93, p < .001.

Data

Raw and analyzed data can be accessed via Mendeley data [2]. In this section, we will report the correlation coefficients of associations between trait predictors (extraversion, neuroticism) and baseline state measures, as well as between different stress response measures. Additionally, scatterplots of significant associations between baseline states and traits and stress responses are provided. Finally, we report on the sex differences in the timing of the peak stress response reactivity.

Associations between stress response systems

Correlations between stress response systems were computed using Pearson correlations, in particular: between trait predictors (extraversion, neuroticism) and baseline state measures (Table 2), between different stress response measures (Table 2), between trait predictors (extraversion, neuroticism) and baseline state measures per sex (Table 3), and between different stress response measures per sex (Table 3).
Table 2

Correlations between trait predictors (extraversion, neuroticism), baseline state measures, and different stress response measures.

Baseline states and traitsExtraversionNeuroticismBaseline PEPBaseline RSABaseline state approach motivationBaseline state anxietyBaseline CortisolResource-demand appraisalΔPEPΔRSAΔState approach motivationΔState anxietyΔCortisol
Extraversionr
p
Neuroticismr−.34
p.005
Baseline PEPr−.14.26
p.266.038
Baseline RSAr−.15.05.02
p.241.683.867
Baseline state approach motivationr.09.08.04−.01
p.484.545.779.927
Baseline state anxietyr.09.01−.07.25.09
p.464.965.557.040.479
Baseline Cortisolr.22−.11.39−.23−.09.06
p.076.372.001*.066.491.629
Resource-demand appraisalr−.04.09.06.05.12−.17−.16
p.734.470.613.709.347.162.210
ΔPEPr.20.25−.30−.18.05−.07.09−.13
p.125.043.017.208.688.603.504.313
ΔRSAr.05.13.18.49.10−.18.09−.05.23
p.697.315.149<.001**.415.165.465.705.094
ΔState approach motivationr−.12.10−.02−.19.36−.15−.03.13−.04−.05
p.336.416.894.124.003*.220.810.302.785.726
ΔState anxietyr−.11−.04.21−.17<.01.52.03.16−.08.22−.26
p.363.777.092.174.993<.001***.790.197.554.075.035
ΔCortisolr−.13.36−.05−.12−.20−.23−.07.02.43−.16.14.11
p.290.003*.712.332.100.087.572.878<.001*.232.268.372

Note. Significant correlations are shown in bold (FDR-corrected p < .05); ** = significant at α = 0.01 after FDR correction; * = significant at α = 0.05 after FDR correction. PEP = pre-ejection period, RSA = respiratory sinus arrhythmia; Δ = individual reactivity.

Table 3

Correlations between trait predictors (extraversion, neuroticism), baseline state measures, and different stress response measures per sex (women above, men below diagonal).

Baseline states and traitsExtraversionNeuroticismBaseline PEPBaseline RSABaseline state approach motivationBaseline state anxietyBaseline CortisolResource-demand appraisalΔPEPΔRSAΔState approach motivationΔState anxietyΔCortisol
Extraversionr−.38−.34−.18.01.15.38−.03.43−.03−.12−.15−.25
p.035.065.347.951.439.040.857.024.864.539.432.201
Neuroticismr.19.34−.09.17−.12−.14.04.01.42−.08.30−.26
p.252.068.637.370.532.463.816.950.025.689.109.162
Baseline PEPr.14.17.02−.27−.18−.40.03−.34.15.18.16.06
p.414.326.915.150.344.027.873.070.431.356.390.773
Baseline RSAr.09.09.01−.03.16−.19.22−.25−.49−.27−.16.12
p.593.583.947.864.412.335.261.235.011.164.395.553
Baseline state approach motivationr.19.02.30.01−.03−.06.13.23.05−.39−.06−.22
p.266.924.083.976.859.768.502.276.783.032.758.251
Baseline state anxietyr.07.05.03.32.18.09−.11−.05−.07−.17−.51−.20
p.686.776.865.051.276.639.564.797.710.363.004.354
Baseline Cortisolr.05.14.38.28.12.02−.32.02.08−.10.08−.10
p.762.414.023.093.492.912.086.923.677.612.674.638
Resource-demand appraisalr.06.16.10.07.11.23<.01−.18−.15.02.16−.22
p.705.353.566.677.514.174.984.342.458.914.403.251
ΔPEPr.01.44.27.14.08.09.15.08.39−.18−.07−.35
p.951.006.120.466.664.596.415.645.052.387.725.067
ΔRSAr.13.10.25.53.18.31.12.06.06.04.15−.41
p.465.567.160.002.309.069.476.708.735.846.442.030
ΔState approach motivationr.09.22.26.15.35.15.04.25.10.15−.15.16
p.608.184.129.376.031.384.809.144.579.382.441.415
ΔState anxietyr.07.29.24.19.03.57.01.17.09.33.37.11
p.701.079.156.275.883<.001*.971.326.614.047.023.565
ΔCortisolr.10.37.12.27.18.23.04.20.50.10.16.14
p.565.025.473.107.277.165.809.236.003.590.352.416

Note. Men are shown underneath the diagonal in bold; women are shown above the diagonal. * = significant at α = 0.05 after FDR correction. PEP = pre-ejection period, RSA = respiratory sinus arrhythmia; Δ = individual reactivity.

Correlations between trait predictors (extraversion, neuroticism), baseline state measures, and different stress response measures. Note. Significant correlations are shown in bold (FDR-corrected p < .05); ** = significant at α = 0.01 after FDR correction; * = significant at α = 0.05 after FDR correction. PEP = pre-ejection period, RSA = respiratory sinus arrhythmia; Δ = individual reactivity. Correlations between trait predictors (extraversion, neuroticism), baseline state measures, and different stress response measures per sex (women above, men below diagonal). Note. Men are shown underneath the diagonal in bold; women are shown above the diagonal. * = significant at α = 0.05 after FDR correction. PEP = pre-ejection period, RSA = respiratory sinus arrhythmia; Δ = individual reactivity. For all analyses, alpha was set at .05, and false-discovery rate (FDR) correction was performed to correct for multiple comparisons. Uncorrected p-values are reported for transparency, with FDR-corrected significance indicated by superscript symbols. When combining men and women, the only significant FDR-corrected correlations were those between PEP and cortisol, both for baseline and reactivity indices ‒ indicating more sympathetic nervous system (SNS) activity with more hypothalamus-pituitary-adrenal (HPA) axis activity ‒ as well as between baseline and reactivity for RSA, state approach motivation, and state anxiety, and between neuroticism and Δcortisol. No correlations for each sex separately were significant after FDR-correction.

Scatterplots of significant associations

Scatterplots of significant regression associations between trait predictors (extraversion, neuroticism), baseline state measures, and different stress response measures per sex are shown in Fig. 2. The first imputed dataset (see section: Multiple imputation of missing data) was used for illustration purposes (N = 67).
Fig. 2

Scatterplots of significant associations between trait predictors, baseline state measures, and different stress response measures per sex: a) trait neuroticism with ΔPEP, b) trait neuroticism with Δcortisol, c) baseline PEP with ΔPEP, d) baseline RSA with ΔRSA, e) baseline state approach motivation with Δstate approach motivation, f) baseline state anxiety with Δstate anxiety, and g) ΔPEP with Δcortisol.

Scatterplots of significant associations between trait predictors, baseline state measures, and different stress response measures per sex: a) trait neuroticism with ΔPEP, b) trait neuroticism with Δcortisol, c) baseline PEP with ΔPEP, d) baseline RSA with ΔRSA, e) baseline state approach motivation with Δstate approach motivation, f) baseline state anxiety with Δstate anxiety, and g) ΔPEP with Δcortisol.

Peak timing

Sex differences in the timing of the peak reactivity were assessed using two-sample t-tests (variances not assumed equal). Sex differences in RSA were tested using a linear regression with RR as covariate. The regression coefficients were then converted into t-values. To provide confirming evidence of the null hypotheses, Bayes factors were calculated from t-values using the BayesFactor package [29] with default non-informative priors. Alpha was set at .05, and FDR correction was performed to correct for multiple comparisons. Uncorrected p-values are reported for transparency, with FDR-corrected significance indicated by superscript symbols. Results are shown in Table 4. Peak time of the decrease in RSA (corrected for RR) was earlier in women than men and peak time of the decrease in PEP was comparable between men and women. Peak time reactivity of state anxiety, state approach motivation, mean BP, heart rate, RSA (uncorrected for RR), RR, and cortisol did not differ significantly between men and women, although based on Bayes factors there was inconclusive evidence to support neither equal nor different group means.
Table 4

Sex differences in time of peak reactivity.

SET reactivitySexMeanSDt (df)pBF
ΔState anxietyMale13.813.91.06 (63).2950.40 inc.
Female12.873.4
ΔState approach motivationMale12.513.21.04 (63).3030.40 inc.
Female11.802.4
ΔMean BPMale20.358.50.94 (63).3520.37 inc.
Female22.177.3
ΔHeart rateMale6.521.22.33 (56).0242.40 inc.
Female5.801.2
ΔPEPMale8.215.70.19 (49).8520.26H0
Female8.526.8
ΔRSAMale12.529.41.27 (58).2110.50 inc.
Female9.738.0
ΔRSA (corrected for RR)4.51 (57)<.001***2.62*102H1
ΔRRMale14.989.81.04 (57).3020.40 inc.
Female12.439.4
ΔCortisolMale33.736.01.58 (48).1200.72 inc.
Female30.808.5

Note. Mean peak time in minutes after onset of SET manipulation (duration of 18 minutes). SD = standard deviation; BF = Bayes factor; BP = blood pressure; PEP = pre-ejection period; RSA = respiratory sinus arrhythmia; RR = respiratory rate; Δ = individual reactivity. *** = significant at α = .001 after FDR correction; H0 = evidence in support of equal group estimates; H1 = evidence in support of different group means; inc. = inconclusive evidence in support of neither equal nor different group means.

Sex differences in time of peak reactivity. Note. Mean peak time in minutes after onset of SET manipulation (duration of 18 minutes). SD = standard deviation; BF = Bayes factor; BP = blood pressure; PEP = pre-ejection period; RSA = respiratory sinus arrhythmia; RR = respiratory rate; Δ = individual reactivity. *** = significant at α = .001 after FDR correction; H0 = evidence in support of equal group estimates; H1 = evidence in support of different group means; inc. = inconclusive evidence in support of neither equal nor different group means.

Specifications Table

Subject areaPsychology
More specific subject areaNeuropsychology and Physiological Psychology; Experimental and Cognitive Psychology.
Type of dataTable, Figure, text.
How data was acquiredCardiovascular physiology (electrocardiography and impedance cardiography) and respiration were recorded continuously. Blood pressure, endocrine physiology, and self-reported states were repeatedly measured. Additionally, self-reported traits were assed via questionnaires at the end of the experiment.
Data formatRaw and analyzed
Experimental factorsMale and female participants were 18–35 years of age, right-handed, had normal or corrected- to-normal vision, were currently studying at college or university, were heterosexual, free of psychiatric and endocrinological disorders, not taking medication that could influence cognition, emotion, or hormones, and were not a regular smoker or drinker. Additionally, female participants did not use oral hormonal contraception or an intrauterine device for at least the last three months, were not currently pregnant or breast-feeding, had a regular menstrual cycle, and were tested during the luteal phase of their menstrual cycle.
Experimental featuresA five-minute resting state was measured as a baseline. To induce social-evaluative threat (SET), an impromptu speaking task was used. Participants were first told in the lab that they would give a five-minute speech about their positive and negative personality characteristics. We told participants that their video would later be evaluated by that same audience on ten aspects concerning speech delivery, content, and quality. Participants were given five minutes to prepare their speech (stress condition). During the speech, the video of the neutral pre-recorded audience was shown while a camera recorded their speech. The entire SET manipulation lasted about 18 min. After the speech, a five-minute recovery was measured, and a second recovery 30 minutes later.
Data source locationSalzburg University, Salzburg, Austria
Data accessibilityE.S. Poppelaars, J. Klackl, B. Pletzer, F.H. Wilhelm, E. Jonas, Open dataset for: “Social-evaluative threat: Stress response stages and influences of biological sex and neuroticism”, Mendeley Data. (2019). https://doi.org/10.17632/7vj8r76s6f.
Related research articleE.S. Poppelaars, J. Klackl, B. Pletzer, F.H. Wilhelm, E. Jonas, Social-evaluative threat: Stress response stages and influences of biological sex and neuroticism, Psychoneuroendocrinology. 109 (2019) 104378. https://doi.org/10.1016/j.psyneuen.2019.104378.
Value of the Data

The correlation coefficients could be used in a meta-analysis about associations between stress responses.

The information about the timing of individual stress responses in different systems and their sex differences could inform research on the timing of stress response.

Our approach to missing data management ‒ particularly the use of multiple imputation ‒ can serve to inspire other researchers on how to manage missing data.

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  1 in total

1.  Data for "Social-evaluative threat: Stress response stages and influences of biological sex and neuroticism".

Authors:  Eefje S Poppelaars; Johannes Klackl; Belinda Pletzer; Frank H Wilhelm; Eva Jonas
Journal:  Data Brief       Date:  2019-10-13
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