The Impact of Social Cognition on the Real-Life of People with Epilepsy
Abstract
:1. Introduction
2. Materials and Methods
2.1. Study Sample
2.2. Clinical and Socioeconomic Data
2.3. Tests of Social Cognition
2.4. Data Analysis
3. Results
3.1. General Findings
3.2. Social Cognition and Education
3.3. Social Cognition and Employment
3.4. Relationships and Quality of Life
4. Discussion
4.1. Social Cognition and Epilepsy
4.2. Real-Life Outcomes in the Context of Social Cognition
4.2.1. Social Cognition and Education
4.2.2. Social Cognition and Employment
4.2.3. Social Cognition and Relationships
4.3. Study Limitations
5. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
References
- Fisher, R.S.; van Emde Boas, W.; Blume, W.; Elger, C.; Genton, P.; Lee, P.; Engel, J., Jr. Epileptic Seizures and Epilepsy: Definitions proposed by the International League against Epilepsy (ILAE) and the International Bureau for Epilepsy (IBE). Epilepsia 2005, 46, 1701–1702. [Google Scholar] [CrossRef]
- Steiger, B.K.; Jokeit, H. Why epilepsy challenges social life. Seizure 2017, 44, 194–198. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Guida, M.; Caciagli, L.; Cosottini, M.; Bonuccelli, U.; Fornai, F.; Giorgi, F.S. Social cognition in idiopathic generalized epilepsies and potential neuroanatomical correlates. Epilepsy Behav. 2019, 100, 106118. [Google Scholar] [CrossRef]
- Morou, N.; Papaliagkas, V.; Markouli, E.; Karagianni, M.; Nazlidou, E.; Spilioti, M.; Afrantou, T.; Kimiskidis, V.K.; Foroglou, N.; Kosmidis, M. Theory of Mind impairment in focal versus generalized epilepsy. Epilepsy Behav. 2018, 88, 244–250. [Google Scholar] [CrossRef]
- Bora, E.; Meletti, S. Social cognition in temporal lobe epilepsy: A systematic review and meta-analysis. Epilepsy Behav. 2016, 60, 50–57. [Google Scholar] [CrossRef] [PubMed]
- Realmuto, S.; Zummo, L.; Cerami, C.; Agrò, L.; Dodich, A.; Canessa, N.; Zizzo, A.; Fierro, B.; Daniele, O. Social cognition dysfunctions in patients with epilepsy: Evidence from patients with temporal lobe and idiopathic generalized epilepsies. Epilepsy Behav. 2015, 47, 98–103. [Google Scholar] [CrossRef] [PubMed]
- Giovagnoli, A.R.; Parente, A.; Villani, F.; Franceschetti, S.; Spreafico, R. Theory of mind and epilepsy: What clinical implications? Epilepsia 2013, 54, 1639–1646. [Google Scholar] [CrossRef]
- Wang, W.-H.; Shih, Y.-H.; Yu, H.-Y.; Yen, D.-J.; Lin, Y.-Y.; Kwan, S.-Y.; Chen, C.; Hua, M.-S. Theory of mind and social functioning in patients with temporal lobe epilepsy. Epilepsia 2015, 56, 1117–1123. [Google Scholar] [CrossRef]
- Giovagnoli, A.R. Awareness, overestimation, and underestimation of cognitive functions in epilepsy. Epilepsy Behav. 2013, 26, 75–80. [Google Scholar] [CrossRef]
- O’Donoghue, M.F.; Duncan, J.S.; Sander, J. The National Hospital Seizure Severity Scale: A Further Development of the Chalfont Seizure Severity Scale. Epilepsia 1996, 37, 563–571. [Google Scholar] [CrossRef]
- Gilliam, F.G.; Barry, J.J.; Hermann, B.P.; Meador, K.J.; Vahle, V.; Kanner, A.M. Rapid detection of major depression in epilepsy: A multicentre study. Lancet Neurol. 2006, 5, 399–405. [Google Scholar] [CrossRef]
- Cramer, J.A.; Perrine, K.; Devinsky, O.; Bryant-Comstock, L.; Meador, K.; Hermann, B. Development and Cross-Cultural Translations of a 31-Item Quality of Life in Epilepsy Inventory. Epilepsia 1998, 39, 81–88. [Google Scholar] [CrossRef]
- International Labour Office. International Standard Classification of Occupations. 1 v.; International Labour Office: Geneva, Switzerland, 2012. [Google Scholar]
- The Organisation for Economic Co-operation and Development, European Union, UNESCO Institute of Statistics. ISCED 2011 Operational Manual; OECD Publishing: Paris, France, 2015. [Google Scholar]
- Baron-Cohen, S.; Wheelwright, S.; Hill, J.; Raste, Y.; Plumb, I. The “Reading the Mind in the Eyes” Test revised version: A study with normal adults, and adults with Asperger syndrome or high-functioning autism. J. Child Psychol. Psychiatry 2001, 42, 241–251. [Google Scholar] [CrossRef]
- Baron-Cohen, S.; O’Riordan, M.; Stone, V.; Jones, R.; Plaisted, K. Recognition of Faux Pas by Normally Developing Children and Children with Asperger Syndrome or High-Functioning Autism. J. Autism Dev. Disord. 1999, 29, 407–418. [Google Scholar] [CrossRef]
- Happé, F.G.E. An advanced test of theory of mind: Understanding of story characters’ thoughts and feelings by able autistic, mentally handicapped, and normal children and adults. J. Autism Dev. Disord. 1994, 24, 129–154. [Google Scholar] [CrossRef] [PubMed]
- Fletcher, P.; Happé, F.; Frith, U.; Baker, S.; Dolan, R.; Frackowiak, R.; Frith, C. Other minds in the brain: A functional imaging study of “theory of mind” in story comprehension. Cognition 1995, 57, 109–128. [Google Scholar] [CrossRef] [Green Version]
- Jasionis, A.; Jasionytė, G.; Mameniškienė, R. Faux pas atpažinimo ir Happé keistų istorijų testų lietuviškų versijų adaptacija bei psichometrinių savybių vertinimas. Neurol. Semin. 2020, 24, 47–54. [Google Scholar] [CrossRef]
- Giovagnoli, A.R.; Franceschetti, S.; Reati, F.; Parente, A.; Maccagnano, C.; Villani, F.; Spreafico, R. Theory of mind in frontal and temporal lobe epilepsy: Cognitive and neural aspects. Epilepsia 2011, 52, 1995–2002. [Google Scholar] [CrossRef]
- Broicher, S.D.; Kuchukhidze, G.; Grunwald, T.; Krämer, G.; Kurthen, M.; Jokeit, H. “Tell me how do I feel”—Emotion recognition and theory of mind in symptomatic mesial temporal lobe epilepsy. Neuropsychologia 2012, 50, 118–128. [Google Scholar] [CrossRef]
- Gomez-Ibañez, A.; Urrestarazu, E.; Viteri, C. Recognition of facial emotions and identity in patients with mesial temporal lobe and idiopathic generalized epilepsy: An eye-tracking study. Seizure 2014, 23, 892–898. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Edwards, M.; Stewart, E.; Palermo, R.; Lah, S. Facial emotion perception in patients with epilepsy: A systematic review with meta-analysis. Neurosci. Biobehav. Rev. 2017, 83, 212–225. [Google Scholar] [CrossRef] [Green Version]
- Reynders, H.J.; Broks, P.; Dickson, J.M.; Lee, C.E.; Turpin, G. Investigation of social and emotion information processing in temporal lobe epilepsy with ictal fear. Epilepsy Behav. 2005, 7, 419–429. [Google Scholar] [CrossRef]
- Jokeit, H.; Ives-Deliperi, V.; Eicher, M. Toward a social neuropsychology of epilepsy: A review on social congition in epi-lepsies. Acta Epilepsy 2018, 1, 8–17. [Google Scholar] [CrossRef]
- Elger, C.E.; Helmstaedter, C.; Kurthen, M. Chronic epilepsy and cognition. Lancet Neurol. 2004, 3, 663–672. [Google Scholar] [CrossRef]
- Stewart, E.; Lah, S.; Smith, M.L. Patterns of impaired social cognition in children and adolescents with epilepsy: The borders between different epilepsy phenotypes. Epilepsy Behav. 2019, 100, 106146. [Google Scholar] [CrossRef] [PubMed]
- Bonora, A.; Benuzzi, F.; Monti, G.; Mirandola, L.; Pugnaghi, M.; Nichelli, P.; Meletti, S. Recognition of emotions from faces and voices in medial temporal lobe epilepsy. Epilepsy Behav. 2011, 20, 648–654. [Google Scholar] [CrossRef] [PubMed]
- Mirabel, H.; Guinet, V.; Voltzenlogel, V.; Pradier, S.; Hennion, S. Social cognition in epilepsy: State of the art and perspectives. Rev. Neurol. 2020, 176, 468–479. [Google Scholar] [CrossRef]
- Hennion, S.; Delbeuck, X.; Duhamel, A.; Lopes, R.; Semah, F.; Tyvaert, L.; Derambure, P.; Szurhaj, W. Characterization and prediction of theory of mind disorders in temporal lobe epilepsy. Neuropsychology 2015, 29, 485–492. [Google Scholar] [CrossRef]
- Giovagnoli, A.R. Theory of mind across lifespan from ages 16 to 81 years. Epilepsy Behav. 2019, 100, 106349. [Google Scholar] [CrossRef]
- Meinhardt-Injac, B.; Daum, M.M.; Meinhardt, G. Theory of mind development from adolescence to adulthood: Testing the two-component model. Br. J. Dev. Psychol. 2020, 38, 289–303. [Google Scholar] [CrossRef] [Green Version]
- Giovagnoli, A.R. The importance of theory of mind in epilepsy. Epilepsy Behav. 2014, 39, 145–153. [Google Scholar] [CrossRef] [PubMed]
- Wang, Y.; Su, Y. Theory of mind in old adults: The performance on happe’s stories and faux pas stories. Psychologia 2006, 49, 228–237. [Google Scholar] [CrossRef]
- Zalla, T.; Korman, J. Prior Knowledge, Episodic Control and Theory of Mind in Autism: Toward an Integrative Account of Social Cognition. Front. Psychol. 2018, 9, 752. [Google Scholar] [CrossRef] [Green Version]
- Witt, J.-A.; Helmstaedter, C. Cognition in epilepsy: Current clinical issues of interest. Curr. Opin. Neurol. 2017, 30, 174–179. [Google Scholar] [CrossRef]
- Eddy, C.M. What Do You Have in Mind? Measures to Assess Mental State Reasoning in Neuropsychiatric Populations. Front. Psychiatry 2019, 10, 425. [Google Scholar] [CrossRef] [Green Version]
- Wlodarski, R.; Dunbar, R.I.M. The Effects of Romantic Love on Mentalizing Abilities. Rev. Gen. Psychol. 2014, 18, 313–321. [Google Scholar] [CrossRef] [Green Version]
- Dodell-Feder, D.; Felix, S.; Yung, M.G.; Hooker, C.I. Theory-of-mind-related neural activity for one’s romantic partner predicts partner well-being. Soc. Cogn. Affect. Neurosci. 2015, 11, 593–603. [Google Scholar] [CrossRef] [Green Version]
- Lecce, S.; Ceccato, I.; Bianco, F.; Rosi, A.; Bottiroli, S.; Cavallini, E. Theory of Mind and social relationships in older adults: The role of social motivation. Aging Ment. Heal. 2017, 21, 253–258. [Google Scholar] [CrossRef]
- Tedrus, G.M.A.S.; Fonseca, L.C.; Pereira, R.B. Marital status of patients with epilepsy: Factors and quality of life. Seizure 2015, 27, 66–70. [Google Scholar] [CrossRef] [Green Version]
- Riasi, H.; Sanati, A.R.; Ghaemi, K. The stigma of epilepsy and its effects on marital status. SpringerPlus 2014, 3, 762. [Google Scholar] [CrossRef] [PubMed] [Green Version]
GGE (n = 27) | ETE (n = 29) | TLE (n = 25) | Test Value | Significance | |
---|---|---|---|---|---|
n (%), Median (Range) or Mean (SD) | |||||
Male/female | 5 (18.5%)/22 (81.5%) | 13 (44.8%)/16 (55.2%) | 13 (52.0%)/12 (48.0%) | χ2 = 6.981 | 0.030 * |
Age (years) | 26 (18–42) | 30 (19–66) | 36 (23–57) | H = 13.635 | 0.001 * |
Years with epilepsy | 11.67 (7.67) | 16.86 (9.27) | 16.92 (10.89) | F = 2.823 | 0.066 |
ASMs | H = 8.261 | 0.016 * | |||
None | 3 (11.1%) | 1 (3.4%) | 0 | ||
1 | 14 (51.9%) | 8 (27.6%) | 10 (40.0%) | ||
2 | 6 (22.2%) | 8 (27.6%) | 5 (20.0%) | ||
3 | 3 (11.1%) | 8 (27.6%) | 3 (12.0%) | ||
≥4 | 1 (3.7%) | 4 (13.7%) | 7 (28.0%) | ||
Etiology | χ2 = 73.378 | <0.0001 ** | |||
Genetic | 27 (100%) | 1 (3.4%) | 2 (8.0%) | ||
Structural | 8 (27.6%) | 12 (48.0%) | |||
Unknown | 20 (69.0%) | 11 (44.0%) | |||
MRI lesion | 2, 7.4% (0 seizure-related) | 11, 37.9% (7 seizure-related) | 18, 72% (17 seizure-related) | 32.543 | <0.0001 ** |
Experiences GTCS | 25 (92.6%) | 20 (69.0%) | 16 (64.0%) | χ2 = 6.685 | 0.035 * |
GTCS frequency 1 | 2 (1–3) | 2 (1–5) | 1.5 (1–5) | H = 0.054 | 0.974 |
GTCS severity | 15.04 (2.85) | 15.40 (4.48) | 14.14 (3.90) | F = 0.484 | 0.619 |
Experiences other seizures than GTCS | 17 (63.0%) | 24 (82.8%) | 24 (96.0%) | χ2 = 9.118 | 0.010 * |
Non-GTCS frequency 1 | 3 (1–5) | 3 (2–5) | 3 (1–5) | H = 2.465 | 0.292 |
Non-GTCS severity | 1 (1–7) | 6 (1–12) | 4 (1–12) | H = 17.929 | <0.0001 ** |
NDDI-E | 9 (6–20) | 12 (6–20) | 11 (6–24) | H = 4.034 | 0.133 |
Years in the education system | 14 (9–17) | 13 (9–22) | 15 (6–20) | H = 6.038 | 0.049 * |
ISCED | 4 (2–6) | 3 (2–7) | 5 (1–7) | H = 4.886 | 0.087 |
Tertiary education | 12 (44.4%) | 5 (17.2%) | 13 (52.0%) | χ2 = 7.909 | 0.019 * |
Is employed | 16 (59.3%) | 17 (58.6%) | 17 (68.0%) | χ2 = 0.604 | 0.739 |
ISCO 1–3 (high level of skill) | 10 (62.5%) | 5 (29.4%) | 12 (70.6%) | χ2 = 6.486 | 0.039 * |
Has a partner/widowed | 17 (63.0%) | 13 (44.8%) | 13 (54.2%) | χ2 = 1.852 | 0.396 |
Partner status | 7.997 | 0.409 | |||
Single | 8 (29.6%) | 13 (44.8%) | 10 (40.0%) | ||
Married | 8 (29.6%) | 9 (31.0%) | 10 (40.0%) | ||
In a relationship | 9 (33.3%) | 3 (10.3%) | 3 (12.0%) | ||
Divorced | 2 (7.4%) | 3 (10.3%) | 1 (4.0%) | ||
Widow | 0 | 1 (3.4%) | 0 | ||
Unknown | 0 | 0 | 1 (4.0%) | ||
Children | 5.828 | 0.407 | |||
0 | 16 (59.3%) | 18 (62.1%) | 14 (56.0%) | ||
1 | 6 (22.2%) | 7 (24.1%) | 2 (8.0%) | ||
2 | 5 (18.5%) | 3 (10.3%) | 7 (28.0%) | ||
3 | 0 | 1 (3.4%) | 1 (4.0%) | ||
Unknown | 0 | 0 | 1 (4.0%) |
GGE (n = 27) | ETE (n = 29) | TLE (n = 25) | HC (n = 30) | Test Value | Significance | |
---|---|---|---|---|---|---|
Median (Range) or Mean (SD) | ||||||
Faux pas recognition test | ||||||
Number of faux pas stories detected | 5 (1–6) | 5 (2–6) | 5 (1–6) | 5 (2–6) | H = 3.621 | 0.305 |
Number of control stories detected 1 | 3 (0–3) | 3 (0–3) | 3 (0–3) | 3 (2–3) | H = 8.339 | 0.040 * HC > TLE/ETE/GGE 2 |
Faux pas detection in the stories | 10 (2–12) | 10 (4–12) | 9 (2–12) | 10 (4–12) | H = 2.993 | 0.393 |
Understanding Inappropriateness | 4 (0–6) | 4 (0–6) | 4 (0–6) | 5 (2–6) | H = 5.635 | 0.131 |
Intentions | 2 (0–5) | 2 (0–5) | 1 (0–4) | 4 (0–6) | H = 30.890 | <0.0001 * HC > TLE/ETE/GGE |
Belief | 3 (0–5) | 3 (1–6) | 3 (0–6) | 4 (0–6) | H = 6.506 | 0.089 |
Empathy | 4 (1–6) | 4 (1–6) | 4 (0–6) | 5 (1–6) | H = 6.771 | 0.080 |
Faux pas total score | 21.19 (6.87) | 23.45 (6.47) | 19.24 (8.66) | 25.20 (7.98) | F = 3.284 | 0.024 * HC > TLE |
Happé strange stories test | 13 (5–15) | 12 (3–16) | 11 (2–15) | 14 (10–16) | H = 18.997 | <0.0001 * HC > ETE/TLE |
Reading of the Mind in the Eyes test | 24.85 (4.83) | 23.48 (3.491) | 23.04 (6.45) | n/t | F = 0.946 | 0.393 |
Quality of life3 | ||||||
Seizure worry | 49.98 (31.04) | 53.15 (27.84) | 43.20 (29.06) | n/a | F = 0.745 | 0.478 |
Overall QoL | 77.5 (32.5–100) | 66.25 (15–90) | 60 (32.5–82.5) | n/a | H = 6.181 | 0.045 * GGE > TLE |
Emotional well-Being | 68.65 (22.10) | 60.68 (18.39) | 58.61 (22.58) | n/a | F = 1.615 | 0.206 |
Energy/Fatigue | 55.77 (20.82) | 53.63 (16.93) | 47.93 (23.56) | n/a | F = 0.951 | 0.391 |
Cognitive | 61.43 (24.40) | 61.32 (19.78) | 52.52 (22.59) | n/a | F = 1.275 | 0.286 |
Medication effects | 66.02 (24.59) | 71.32 (19.73) | 61.23 (28.65) | n/a | F = 1.099 | 0.339 |
Social function | 87.5 (24–100) | 66 (13–100) | 77 (0–100) | n/a | H = 2.214 | 0.331 |
QOLIE-31 total score | 65.78 (18.10) | 61.03 (15.85) | 56.73 (18.61) | n/a | F = 1.642 | 0.201 |
ISCED | Employment | |||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Independent Variable | Univariable Models | Multivariable Model 1,2 | Univariable Models | Multivariable Model 1,3 | ||||||||
B Coefficient | p Value | OR (95% CI) | B Coefficient | p Value | OR (95% CI) | B Coefficient | p Value | OR (95% CI) | B Coefficient | p Value | OR (95% CI) | |
Duration of epilepsy | −0.370 | 0.099 | 0.96 (0.92 to 1.01) | 0.003 | 0.895 | 1.00 (0.96 to 1.05) | −0.019 | 0.422 | 0.98 (0.94 to 1.03) | 0.040 | 0.229 | 1.04 (0.98 to 1.11) |
Number of ASMs | −0.436 | 0.009 | 0.65 (0.47 to 0.90) | −0.213 | 0.327 | 0.81 (0.53 to 1.24) | −0.505 | 0.009 | 0.60 (0.41 to 0.88) | −0.093 | 0.752 | 0.91 (0.51 to 1.62) |
Seizure frequency | −0.266 | 0.113 | 0.77 (0.55 to 1.07) | 0.053 | 0.800 | 1.06 (0.70 to 1.59) | −0.548 | 0.010 | 0.58 (0.38 to 0.88) | −0.309 | 0.296 | 0.73 (0.41 to 1.31) |
NDDI-E | −0.141 | 0.008 | 0.87 (0.78 to 0.96) | −0.090 | 0.101 | 0.91 (0.82 to 1.02) | −0.099 | 0.095 | 0.91 (0.81 to 1.02) | −0.024 | 0.739 | 0.98 (0.85 to 1.12) |
RMET | 0.199 | <0.0001 | 1.22 (1.12 to 1.33) | 0.196 | <0.0001 | 1.22 (1.09 to 1.36) | 0.178 | 0.002 | 1.20 (1.07 to 1.34) | 0.104 | 0.138 | 1.11 (0.97 to 1.27) |
HST | 0.249 | <0.0001 | 1.28 (1.14 to 1.44) | 0.180 | 0.025 | 1.20 (1.02 to 1.40) | 0.282 | <0.0001 | 1.33 (1.14 to 1.54) | 0.260 | 0.011 | 1.30 (1.06 to 1.58) |
FPRT | 0.040 | 0.130 | 1.04 (0.99 to 1.10) | −0.070 | 0.044 | 0.93 (0.87 to 1.00) | 0.050 | 0.112 | 1.05 (0.99 to 1.12) | −0.033 | 0.481 | 0.97 (0.88 to 1.06) |
Independent Variable | B Coefficient | p Value |
---|---|---|
Duration of epilepsy | 0.072 | 0.407 |
Number of ASMs | −0.123 | 0.226 |
Seizure frequency | −0.171 | 0.062 |
NDDI-E | −0.678 | <0.0001 |
RMET | 0.123 | 0.191 |
HST | −0.193 | 0.067 |
FPRT | 0.010 | 0.916 |
Constant | 102.866 | <0.0001 |
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Jasionis, A.; Puteikis, K.; Mameniškienė, R. The Impact of Social Cognition on the Real-Life of People with Epilepsy. Brain Sci. 2021, 11, 877. https://doi.org/10.3390/brainsci11070877
Jasionis A, Puteikis K, Mameniškienė R. The Impact of Social Cognition on the Real-Life of People with Epilepsy. Brain Sciences. 2021; 11(7):877. https://doi.org/10.3390/brainsci11070877
Chicago/Turabian StyleJasionis, Arminas, Kristijonas Puteikis, and Rūta Mameniškienė. 2021. "The Impact of Social Cognition on the Real-Life of People with Epilepsy" Brain Sciences 11, no. 7: 877. https://doi.org/10.3390/brainsci11070877
APA StyleJasionis, A., Puteikis, K., & Mameniškienė, R. (2021). The Impact of Social Cognition on the Real-Life of People with Epilepsy. Brain Sciences, 11(7), 877. https://doi.org/10.3390/brainsci11070877