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Alexithymia and Somatization in Chronic Pain Patients: A Sequential Mediation Model

OBJECTIVE: To investigate whether chronic pain (CP) patients with somatization reported higher alexithymic traits than those without somatization and to study the different relationships between psychological characteristics, pain, health-related quality of life (HRQL), and somatization. METHOD: A c...

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Autores principales: Lanzara, Roberta, Conti, Chiara, Camelio, Martina, Cannizzaro, Paolo, Lalli, Vittorio, Bellomo, Rosa Grazia, Saggini, Raoul, Porcelli, Piero
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7655126/
https://www.ncbi.nlm.nih.gov/pubmed/33192791
http://dx.doi.org/10.3389/fpsyg.2020.545881
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author Lanzara, Roberta
Conti, Chiara
Camelio, Martina
Cannizzaro, Paolo
Lalli, Vittorio
Bellomo, Rosa Grazia
Saggini, Raoul
Porcelli, Piero
author_facet Lanzara, Roberta
Conti, Chiara
Camelio, Martina
Cannizzaro, Paolo
Lalli, Vittorio
Bellomo, Rosa Grazia
Saggini, Raoul
Porcelli, Piero
author_sort Lanzara, Roberta
collection PubMed
description OBJECTIVE: To investigate whether chronic pain (CP) patients with somatization reported higher alexithymic traits than those without somatization and to study the different relationships between psychological characteristics, pain, health-related quality of life (HRQL), and somatization. METHOD: A consecutive sample of 134 CP treatment-seeking outpatients were evaluated for alexithymia (TAS-20), somatization (PHQ-15), distress (HADS), HRQL (SF-12), and pain (BPI). RESULTS: Patients with somatization (37.04%) reported significantly higher TAS-20 total scores (p < 0.001) and difficulty in identifying feelings (DIF) (p < 0.001) than those without somatization. The somatizer group had also a significantly higher disease duration, severity and interference of pain, distress, and lower HRQL than the non-somatizer group. Hierarchical regression analysis showed that although distress, pain interference and the mental HRQL component are closely related to somatization (R(2) = 0.55), DIF was the strongest predictor of severity of somatization (β = 0.31). A sequential indirect effect from DIF to somatization via distress symptoms and pain interference turned out to be significant [95% CI (0.01, 0.09)]. Support was also found for sequential mediation paths from DIF to somatization via distress and mental HRQL [95% CI (0.01, 0.11)]. CONCLUSIONS: Our results pointed-out that alexithymia, particularly DIF, may be major factor for somatization risk in CP patients. Longitudinal observations are needed for evaluating the role of alexithymia in clinical outcomes.
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spelling pubmed-76551262020-11-13 Alexithymia and Somatization in Chronic Pain Patients: A Sequential Mediation Model Lanzara, Roberta Conti, Chiara Camelio, Martina Cannizzaro, Paolo Lalli, Vittorio Bellomo, Rosa Grazia Saggini, Raoul Porcelli, Piero Front Psychol Psychology OBJECTIVE: To investigate whether chronic pain (CP) patients with somatization reported higher alexithymic traits than those without somatization and to study the different relationships between psychological characteristics, pain, health-related quality of life (HRQL), and somatization. METHOD: A consecutive sample of 134 CP treatment-seeking outpatients were evaluated for alexithymia (TAS-20), somatization (PHQ-15), distress (HADS), HRQL (SF-12), and pain (BPI). RESULTS: Patients with somatization (37.04%) reported significantly higher TAS-20 total scores (p < 0.001) and difficulty in identifying feelings (DIF) (p < 0.001) than those without somatization. The somatizer group had also a significantly higher disease duration, severity and interference of pain, distress, and lower HRQL than the non-somatizer group. Hierarchical regression analysis showed that although distress, pain interference and the mental HRQL component are closely related to somatization (R(2) = 0.55), DIF was the strongest predictor of severity of somatization (β = 0.31). A sequential indirect effect from DIF to somatization via distress symptoms and pain interference turned out to be significant [95% CI (0.01, 0.09)]. Support was also found for sequential mediation paths from DIF to somatization via distress and mental HRQL [95% CI (0.01, 0.11)]. CONCLUSIONS: Our results pointed-out that alexithymia, particularly DIF, may be major factor for somatization risk in CP patients. Longitudinal observations are needed for evaluating the role of alexithymia in clinical outcomes. Frontiers Media S.A. 2020-10-27 /pmc/articles/PMC7655126/ /pubmed/33192791 http://dx.doi.org/10.3389/fpsyg.2020.545881 Text en Copyright © 2020 Lanzara, Conti, Camelio, Cannizzaro, Lalli, Bellomo, Saggini and Porcelli. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Psychology
Lanzara, Roberta
Conti, Chiara
Camelio, Martina
Cannizzaro, Paolo
Lalli, Vittorio
Bellomo, Rosa Grazia
Saggini, Raoul
Porcelli, Piero
Alexithymia and Somatization in Chronic Pain Patients: A Sequential Mediation Model
title Alexithymia and Somatization in Chronic Pain Patients: A Sequential Mediation Model
title_full Alexithymia and Somatization in Chronic Pain Patients: A Sequential Mediation Model
title_fullStr Alexithymia and Somatization in Chronic Pain Patients: A Sequential Mediation Model
title_full_unstemmed Alexithymia and Somatization in Chronic Pain Patients: A Sequential Mediation Model
title_short Alexithymia and Somatization in Chronic Pain Patients: A Sequential Mediation Model
title_sort alexithymia and somatization in chronic pain patients: a sequential mediation model
topic Psychology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7655126/
https://www.ncbi.nlm.nih.gov/pubmed/33192791
http://dx.doi.org/10.3389/fpsyg.2020.545881
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