Atherosclerosis, a chronic inflammatory condition, is the leading cause of cardiovascular disease (CVD) morbidity and mortality worldwide. Intercellular adhesion molecule-1 (ICAM-1) and vascular cell adhesion molecule-1 (VCAM-1) are key mediators of leukocyte-endothelial interactions and drivers of atherosclerotic progression. While optimism-based psychological interventions have demonstrated beneficial effects on several inflammatory biomarkers, their impact on adhesion molecules remains unclear.
Methods
We conducted a randomized controlled trial involving 61 outpatients with stable coronary artery disease (CAD) who had completed cardiac rehabilitation. Participants were randomized to an eight-week group-based optimism training program or an attention-matched cardiac education control. Changes in plasma ICAM-1 and VCAM-1 levels were measured by ELISA at baseline and 16 weeks as well as psychological measures of depression, anxiety, and negative affect.
Results
The optimism intervention significantly improved psychological outcomes, with reductions in depression, anxiety, and negative affect compared to controls (p < 0.05). While post-intervention adhesion molecule levels showed significant between-group differences, effect sizes were small and inconclusive, with no significant group-by-time interactions. Correlation analyses found no significant link between changes in optimism and adhesion molecule levels.
Conclusions
Optimism-based interventions yield meaningful psychological benefits in patients with CAD, though changes in adhesion molecule biomarkers were small and uncertain. High variability in biomarker levels and limited detectable effect sizes highlight the need for larger studies to clarify the clinical significance of these findings.
{"title":"Impact of optimism training on atherosclerotic biomarkers in coronary artery disease: A randomized controlled trial","authors":"Masoumeh Sadeghi , Nasim Kakavand , Mohammadesmaeil Aramesh Boroujeni , Hamidreza Roohafza , Narges Mohammadi , Alireza Aghayousefi , Mohammad Kermani-Alghoraishi","doi":"10.1016/j.jpsychores.2026.112529","DOIUrl":"10.1016/j.jpsychores.2026.112529","url":null,"abstract":"<div><h3>Background</h3><div>Atherosclerosis, a chronic inflammatory condition, is the leading cause of cardiovascular disease (CVD) morbidity and mortality worldwide. Intercellular adhesion molecule-1 (ICAM-1) and vascular cell adhesion molecule-1 (VCAM-1) are key mediators of leukocyte-endothelial interactions and drivers of atherosclerotic progression. While optimism-based psychological interventions have demonstrated beneficial effects on several inflammatory biomarkers, their impact on adhesion molecules remains unclear.</div></div><div><h3>Methods</h3><div>We conducted a randomized controlled trial involving 61 outpatients with stable coronary artery disease (CAD) who had completed cardiac rehabilitation. Participants were randomized to an eight-week group-based optimism training program or an attention-matched cardiac education control. Changes in plasma ICAM-1 and VCAM-1 levels were measured by ELISA at baseline and 16 weeks as well as psychological measures of depression, anxiety, and negative affect.</div></div><div><h3>Results</h3><div>The optimism intervention significantly improved psychological outcomes, with reductions in depression, anxiety, and negative affect compared to controls (<em>p</em> < 0.05). While post-intervention adhesion molecule levels showed significant between-group differences, effect sizes were small and inconclusive, with no significant group-by-time interactions. Correlation analyses found no significant link between changes in optimism and adhesion molecule levels.</div></div><div><h3>Conclusions</h3><div>Optimism-based interventions yield meaningful psychological benefits in patients with CAD, though changes in adhesion molecule biomarkers were small and uncertain. High variability in biomarker levels and limited detectable effect sizes highlight the need for larger studies to clarify the clinical significance of these findings.</div></div>","PeriodicalId":50074,"journal":{"name":"Journal of Psychosomatic Research","volume":"203 ","pages":"Article 112529"},"PeriodicalIF":3.3,"publicationDate":"2026-01-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146081106","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-22DOI: 10.1016/j.jpsychores.2026.112556
Fares Qeadan, Max Moroz, Benjamin Tingey
Context
Adverse childhood experiences (ACEs) are linked to long-term health impacts, including increased pain prevalence. However, the relationship between ACEs and pain presence and pain control among cancer survivors is not well understood.
Objectives
To examine the association between cumulative ACE exposure and (1) the presence of cancer-related physical pain and (2) the current perceived adequacy of pain control among adult survivors in the United States.
Methods
Behavioral Risk Factor Surveillance-System (BRFSS) data from 2019 to 2023 were analyzed, including 19,046 adults with self-reported cancer diagnoses and complete ACE data. Modified Poisson regression estimated crude and adjusted prevalence ratios (PRs, aPRs) for pain presence and pain control. Subgroup analyses were stratified by cancer type. Random forest models assessed ACE domain importance.
Results
A clear dose-response was found between ACEs and pain presence. Each additional ACE was associated with a 6% higher prevalence of pain (aPR = 1.058; 95% CI: 1.005–1.113). Pain prevalence increased from 7.2% (0 ACEs) to 25.4% (8 ACEs). ACEs were not significantly associated with pain control in adjusted models (aPR = 0.994; 95% CI: 0.973–1.016). Stratified analyses revealed stronger associations in certain cancer types, particularly leukemia, pharyngeal, and bladder. Random forest models identified household dysfunction and emotional/sexual abuse as key predictors of pain presence and pain control.
Conclusion
ACEs are significantly associated with pain presence, but not with perceived pain control. These findings underscore the need for ACE-informed screening and trauma-informed care in survivorship planning to address cancer pain.
Key message
Cancer survivors with adverse childhood experiences report higher prevalence of pain, but not significantly lower prevalence of adequate pain control. This study emphasizes the need for trauma-informed care to address the lasting influence of early adversity on cancer-related symptom burden.
{"title":"Adverse childhood experiences and cancer pain: A national cross-sectional analysis of survivors' pain outcomes","authors":"Fares Qeadan, Max Moroz, Benjamin Tingey","doi":"10.1016/j.jpsychores.2026.112556","DOIUrl":"10.1016/j.jpsychores.2026.112556","url":null,"abstract":"<div><h3>Context</h3><div>Adverse childhood experiences (ACEs) are linked to long-term health impacts, including increased pain prevalence. However, the relationship between ACEs and pain presence and pain control among cancer survivors is not well understood.</div></div><div><h3>Objectives</h3><div>To examine the association between cumulative ACE exposure and (1) the presence of cancer-related physical pain and (2) the current perceived adequacy of pain control among adult survivors in the United States.</div></div><div><h3>Methods</h3><div>Behavioral Risk Factor Surveillance-System (BRFSS) data from 2019 to 2023 were analyzed, including 19,046 adults with self-reported cancer diagnoses and complete ACE data. Modified Poisson regression estimated crude and adjusted prevalence ratios (PRs, aPRs) for pain presence and pain control. Subgroup analyses were stratified by cancer type. Random forest models assessed ACE domain importance.</div></div><div><h3>Results</h3><div>A clear dose-response was found between ACEs and pain presence. Each additional ACE was associated with a 6% higher prevalence of pain (aPR = 1.058; 95% CI: 1.005–1.113). Pain prevalence increased from 7.2% (0 ACEs) to 25.4% (8 ACEs). ACEs were not significantly associated with pain control in adjusted models (aPR = 0.994; 95% CI: 0.973–1.016). Stratified analyses revealed stronger associations in certain cancer types, particularly leukemia, pharyngeal, and bladder. Random forest models identified household dysfunction and emotional/sexual abuse as key predictors of pain presence and pain control.</div></div><div><h3>Conclusion</h3><div>ACEs are significantly associated with pain presence, but not with perceived pain control. These findings underscore the need for ACE-informed screening and trauma-informed care in survivorship planning to address cancer pain.</div></div><div><h3>Key message</h3><div>Cancer survivors with adverse childhood experiences report higher prevalence of pain, but not significantly lower prevalence of adequate pain control. This study emphasizes the need for trauma-informed care to address the lasting influence of early adversity on cancer-related symptom burden.</div></div>","PeriodicalId":50074,"journal":{"name":"Journal of Psychosomatic Research","volume":"203 ","pages":"Article 112556"},"PeriodicalIF":3.3,"publicationDate":"2026-01-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146025726","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-22DOI: 10.1016/j.jpsychores.2026.112547
Anna Weronika Szablewska , Bartosz Zając , Martyna Lesińska , Rita Santos - Rocha , Anna Szumilewicz
Background
Gynecological and breast cancers are among the most prevalent malignancies in women. While survival has improved due to advances in treatment, many survivors experience challenges such as body image disturbances and reduced self-esteem. Physical activity has been identified as a potential protective factor, but evidence specific to this population remains limited.
Aim
The aim of this study was to evaluate the differences in body image and self-esteem among physically active and inactive women with a history of gynecological and breast cancer, as compared to active and inactive healthy controls.
Methods
A cross-sectional online survey was conducted in Poland. Participants were allocated to four groups according to cancer status and physical activity: inactive controls (CON-PI), active controls (CON-PA), inactive cancer survivors (CAN-PI), and active cancer survivors (CAN-PA). Physical activity was defined based on World Health Organization recommendations. Body image and self-esteem were assessed using the Body-Esteem Scale for Adolescents and Adults (BESAA) and the Rosenberg Self-Esteem Scale (RSES).
Results
Physically active women reported significantly higher BESAA and RSES scores compared to inactive women. The CAN-PI group consistently showed the lowest scores across all domains, while the CON-PA group reported the highest. Differences were particularly marked in appearance, attribution, and global self-esteem.
Conclusions
Meeting WHO-recommended physical activity levels was associated with more positive body image and higher self-esteem in women after gynecological and breast cancer treatment. The findings highlight the potential role of physical activity in psychosocial well-being and support its inclusion in survivorship care.
{"title":"Associations between physical activity, body esteem, and self-esteem among women with breast and gynecological cancer","authors":"Anna Weronika Szablewska , Bartosz Zając , Martyna Lesińska , Rita Santos - Rocha , Anna Szumilewicz","doi":"10.1016/j.jpsychores.2026.112547","DOIUrl":"10.1016/j.jpsychores.2026.112547","url":null,"abstract":"<div><h3>Background</h3><div>Gynecological and breast cancers are among the most prevalent malignancies in women. While survival has improved due to advances in treatment, many survivors experience challenges such as body image disturbances and reduced self-esteem. Physical activity has been identified as a potential protective factor, but evidence specific to this population remains limited.</div></div><div><h3>Aim</h3><div>The aim of this study was to evaluate the differences in body image and self-esteem among physically active and inactive women with a history of gynecological and breast cancer, as compared to active and inactive healthy controls.</div></div><div><h3>Methods</h3><div>A cross-sectional online survey was conducted in Poland. Participants were allocated to four groups according to cancer status and physical activity: inactive controls (CON-PI), active controls (CON-PA), inactive cancer survivors (CAN-PI), and active cancer survivors (CAN-PA). Physical activity was defined based on World Health Organization recommendations. Body image and self-esteem were assessed using the Body-Esteem Scale for Adolescents and Adults (BESAA) and the Rosenberg Self-Esteem Scale (RSES).</div></div><div><h3>Results</h3><div>Physically active women reported significantly higher BESAA and RSES scores compared to inactive women. The CAN-PI group consistently showed the lowest scores across all domains, while the CON-PA group reported the highest. Differences were particularly marked in appearance, attribution, and global self-esteem.</div></div><div><h3>Conclusions</h3><div>Meeting WHO-recommended physical activity levels was associated with more positive body image and higher self-esteem in women after gynecological and breast cancer treatment. The findings highlight the potential role of physical activity in psychosocial well-being and support its inclusion in survivorship care.</div></div>","PeriodicalId":50074,"journal":{"name":"Journal of Psychosomatic Research","volume":"203 ","pages":"Article 112547"},"PeriodicalIF":3.3,"publicationDate":"2026-01-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146025754","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-22DOI: 10.1016/j.jpsychores.2026.112554
Martine Smeets , Elody Hutten , Peter Verboon , Yvonne Bol , Viviane Thewissen , Ellen M.M. Jongen
Objective
Previous studies have shown a positive relation between retrospectively measured loneliness and somatic complaints. This study investigated the relation between state loneliness and state somatic complaints as well as the direction of this relation in the context of daily life. It was hypothesized that there is a positive contemporaneous association between state loneliness and state somatic complaints as well as a positive bidirectional temporal association.
Methods
Using the Experience Sampling Method, 16 patients with somatic symptom disorder and 27 participants from the general population received a signal on their smartphones 10 times a day for 14 days to fill out an ESM-item on loneliness and two on somatic complaints. To test our hypotheses, multilevel linear regression models with random effects were estimated.
Results
Associations between state loneliness and state somatic complaints in the context of daily life were demonstrated (B = 0.12, SE = 0.01, p < .001). Temporal analyses revealed, however, that state loneliness (t-1) did not predict somatic complaints (t) in daily life (90-min window; B = 0.01, SE = 0.01, p = .573). Neither did state somatic complaints predict state loneliness (B = 0.02, SE = 0.03, p = .534).
Conclusions
This study demonstrated contemporaneous associations between state loneliness and state somatic complaints in the context of daily life. However, state loneliness did not predict subsequent state somatic complaints, nor did state somatic complaints predict subsequent state loneliness. Future studies are necessary to further disentangle the complex relationship between loneliness and somatic complaints.
目的以往的研究表明,回顾性测量的孤独感与躯体抱怨之间存在正相关关系。本研究探讨了状态孤独与状态躯体抱怨的关系,以及这种关系在日常生活中的走向。假设状态孤独与状态躯体抱怨之间存在正相关,同时存在正相关的双向时间关系。方法采用体验抽样法,选取16例躯体症状障碍患者和27例普通人群,在14天内每天10次通过智能手机接收信号,填写一份关于孤独感的esm项目和两份关于躯体抱怨的esm项目。为了检验我们的假设,我们估计了具有随机效应的多水平线性回归模型。结果在日常生活情境下,状态孤独与状态躯体抱怨之间存在相关性(B = 0.12, SE = 0.01, p < 0.001)。然而,时间分析显示,状态孤独(t-1)不能预测日常生活中的躯体抱怨(t)(90分钟窗口;B = 0.01, SE = 0.01, p = .573)。状态躯体抱怨也不能预测状态孤独(B = 0.02, SE = 0.03, p = .534)。结论:本研究证明了日常生活中状态孤独和状态躯体抱怨之间的同步关联。然而,状态孤独并不能预测随后的状态躯体抱怨,状态躯体抱怨也不能预测随后的状态孤独。未来的研究有必要进一步理清孤独与躯体抱怨之间的复杂关系。
{"title":"Loneliness and somatic complaints: An experience sampling method study","authors":"Martine Smeets , Elody Hutten , Peter Verboon , Yvonne Bol , Viviane Thewissen , Ellen M.M. Jongen","doi":"10.1016/j.jpsychores.2026.112554","DOIUrl":"10.1016/j.jpsychores.2026.112554","url":null,"abstract":"<div><h3>Objective</h3><div>Previous studies have shown a positive relation between retrospectively measured loneliness and somatic complaints. This study investigated the relation between state loneliness and state somatic complaints as well as the direction of this relation in the context of daily life. It was hypothesized that there is a positive contemporaneous association between state loneliness and state somatic complaints as well as a positive bidirectional temporal association.</div></div><div><h3>Methods</h3><div>Using the Experience Sampling Method, 16 patients with somatic symptom disorder and 27 participants from the general population received a signal on their smartphones 10 times a day for 14 days to fill out an ESM-item on loneliness and two on somatic complaints. To test our hypotheses, multilevel linear regression models with random effects were estimated.</div></div><div><h3>Results</h3><div>Associations between state loneliness and state somatic complaints in the context of daily life were demonstrated (B = 0.12, SE = 0.01, <em>p</em> < .001). Temporal analyses revealed, however, that state loneliness (t-1) did not predict somatic complaints (t) in daily life (90-min window; B = 0.01, SE = 0.01, <em>p</em> = .573). Neither did state somatic complaints predict state loneliness (B = 0.02, SE = 0.03, <em>p</em> = .534).</div></div><div><h3>Conclusions</h3><div>This study demonstrated contemporaneous associations between state loneliness and state somatic complaints in the context of daily life. However, state loneliness did not predict subsequent state somatic complaints, nor did state somatic complaints predict subsequent state loneliness. Future studies are necessary to further disentangle the complex relationship between loneliness and somatic complaints.</div></div>","PeriodicalId":50074,"journal":{"name":"Journal of Psychosomatic Research","volume":"203 ","pages":"Article 112554"},"PeriodicalIF":3.3,"publicationDate":"2026-01-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146025755","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-21DOI: 10.1016/j.jpsychores.2026.112553
Liping Sun , Yuexia Liao , Zhi'e Gu , Xiaojuan Wan , Ningning Liu
Objective
To examine longitudinal associations among depressive symptoms, loneliness, and social participation in stroke survivors, and the temporal role of loneliness between social participation and depressive symptoms.
Methods
277 stroke survivors were conveniently sampled from two tertiary hospitals in Yangzhou, China. Depressive symptoms, loneliness, and social participation were assessed using the Patient Health Questionnaire-9, UCLA Loneliness Scale, and Utrecht Scale for Evaluation of Rehabilitation-Participation, respectively. Data were collected at baseline (T1), 3 months (T2), and 6 months (T3) post-stroke, with a cross-lagged panel model used to examine the reciprocal relationships among variables.
Results
Cross-lagged panel analysis revealed: T1 depressive symptoms positively predicted T2 loneliness (β = 0.133, P = 0.046);T1 social participation negatively predicted T2 loneliness (β = −0.226, P < 0.001) and depressive symptoms (β = −0.256, P < 0.001);T2 depressive symptoms negatively predicted T3 social participation (β = −0.098, P = 0.027);T2 loneliness positively predicted T3 depressive symptoms (β = 0.171, P = 0.006);T2 social participation negatively predicted T3 loneliness (β = −0.174, P = 0.001). Mediation analysis showed T2 loneliness mediated T1 social participation's effect on T3 depressive symptoms (indirect effect = −0.037, 95% CI [−0.082, −0.010]).
Conclusion
Alternating cross-lagged effects were observed among depressive symptoms, loneliness, and social participation in stroke survivors, with loneliness potentially acting as a mediator between social participation and subsequent depressive symptoms. These findings suggest hypotheses for phase-specific interventions, which should be tested in future studies.
目的探讨脑卒中幸存者抑郁症状、孤独感和社会参与之间的纵向关系,以及孤独感在社会参与和抑郁症状之间的时间作用。方法从扬州市两所三级医院抽取277例脑卒中幸存者。抑郁症状、孤独感和社会参与分别采用患者健康问卷-9、UCLA孤独感量表和乌得勒支康复参与评估量表进行评估。在脑卒中后基线(T1)、3个月(T2)和6个月(T3)收集数据,采用交叉滞后面板模型来检验变量之间的倒数关系。结果交叉滞后面板分析显示:T1抑郁症状正预测T2孤独(β = - 0.226, P < 0.001)和抑郁症状(β = - 0.256, P < 0.001);T2抑郁症状负预测T3社会参与(β = - 0.098, P = 0.027);T2孤独正预测T3抑郁症状(β = 0.171, P = 0.006);T2社会参与负预测T3孤独(β = - 0.174, P = 0.001)。中介分析显示T2孤独感介导T1社会参与对T3抑郁症状的影响(间接效应= - 0.037,95% CI[- 0.082, - 0.010])。结论脑卒中幸存者抑郁症状、孤独感和社会参与之间存在交变滞后效应,孤独感可能在社会参与与随后的抑郁症状之间起中介作用。这些发现提出了针对特定阶段干预措施的假设,这些假设应该在未来的研究中得到检验。
{"title":"The association among social participation, loneliness and depression in stroke survivors: A longitudinal cross-lagged panel analysis","authors":"Liping Sun , Yuexia Liao , Zhi'e Gu , Xiaojuan Wan , Ningning Liu","doi":"10.1016/j.jpsychores.2026.112553","DOIUrl":"10.1016/j.jpsychores.2026.112553","url":null,"abstract":"<div><h3>Objective</h3><div>To examine longitudinal associations among depressive symptoms, loneliness, and social participation in stroke survivors, and the temporal role of loneliness between social participation and depressive symptoms.</div></div><div><h3>Methods</h3><div>277 stroke survivors were conveniently sampled from two tertiary hospitals in Yangzhou, China. Depressive symptoms, loneliness, and social participation were assessed using the Patient Health Questionnaire-9, UCLA Loneliness Scale, and Utrecht Scale for Evaluation of Rehabilitation-Participation, respectively. Data were collected at baseline (T1), 3 months (T2), and 6 months (T3) post-stroke, with a cross-lagged panel model used to examine the reciprocal relationships among variables.</div></div><div><h3>Results</h3><div>Cross-lagged panel analysis revealed: T1 depressive symptoms positively predicted T2 loneliness (<em>β</em> = 0.133, <em>P</em> = 0.046);T1 social participation negatively predicted T2 loneliness (<em>β</em> = −0.226, <em>P</em> < 0.001) and depressive symptoms (<em>β</em> = −0.256, <em>P</em> < 0.001);T2 depressive symptoms negatively predicted T3 social participation (<em>β</em> = −0.098, <em>P</em> = 0.027);T2 loneliness positively predicted T3 depressive symptoms (<em>β</em> = 0.171, <em>P</em> = 0.006);T2 social participation negatively predicted T3 loneliness (<em>β</em> = −0.174, <em>P</em> = 0.001). Mediation analysis showed T2 loneliness mediated T1 social participation's effect on T3 depressive symptoms (indirect effect = −0.037, 95% <em>CI</em> [−0.082, −0.010]).</div></div><div><h3>Conclusion</h3><div>Alternating cross-lagged effects were observed among depressive symptoms, loneliness, and social participation in stroke survivors, with loneliness potentially acting as a mediator between social participation and subsequent depressive symptoms. These findings suggest hypotheses for phase-specific interventions, which should be tested in future studies.</div></div>","PeriodicalId":50074,"journal":{"name":"Journal of Psychosomatic Research","volume":"203 ","pages":"Article 112553"},"PeriodicalIF":3.3,"publicationDate":"2026-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146015598","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-21DOI: 10.1016/j.jpsychores.2026.112552
Svetlana Blitshteyn , Blair P. Grubb
{"title":"Distress in postural orthostatic tachycardia syndrome (POTS) is largely driven by ineffective healthcare, not patients' attitudes","authors":"Svetlana Blitshteyn , Blair P. Grubb","doi":"10.1016/j.jpsychores.2026.112552","DOIUrl":"10.1016/j.jpsychores.2026.112552","url":null,"abstract":"","PeriodicalId":50074,"journal":{"name":"Journal of Psychosomatic Research","volume":"203 ","pages":"Article 112552"},"PeriodicalIF":3.3,"publicationDate":"2026-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146025727","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Advances in breast cancer treatment have improved survival, making Quality of Life (QOL) a critical endpoint. This study examines longitudinal QOL in Indian breast cancer survivors using the Functional Assessment of Cancer Therapy for Breast (FACT-B) questionnaire.
Methods
A longitudinal cohort study followed 338 women with curable breast cancer, assessing QOL at baseline (before treatment), 3 months, 6 months, 12 months, and 24 months post-treatment. The FACT-B provided total and subscale scores (Physical, Social, Emotional, Functional, and Breast-specific well-being).
Results
Of 338 patients, 63 (18.64%) completed all assessments up to 24 months, and 68 (20.12%) completed up to 12 months. QOL decreased significantly at 3 months post-treatment (mean 74.98 vs. 85.6 at baseline, p < 0.001), remained below baseline at 6 months (79.34, p < 0.001), returned to baseline by 12 months (87.94, p = 0.147), and improved significantly by 24 months (110.92, p < 0.001). Physical and Functional well-being showed early declines, Social and Emotional well-being remained stable or improved, and Breast-specific well-being remained low, reflecting body image concerns.
Conclusion
The U-shaped QOL trajectory highlights the need for interventions at 3–6 months post-treatment, particularly for body image and physical function. These findings provide a foundation for targeted supportive care in Indian breast cancer survivors.
{"title":"Quality of life trajectory in breast cancer survivors: A longitudinal, two-year post treatment follow-up study","authors":"Aashruti Pathania , SreeRekha KR , K. Ramdas , Ankita Chakrawal , Manoj Pandey","doi":"10.1016/j.jpsychores.2026.112551","DOIUrl":"10.1016/j.jpsychores.2026.112551","url":null,"abstract":"<div><h3>Background</h3><div>Advances in breast cancer treatment have improved survival, making Quality of Life (QOL) a critical endpoint. This study examines longitudinal QOL in Indian breast cancer survivors using the Functional Assessment of Cancer Therapy for Breast (FACT-B) questionnaire.</div></div><div><h3>Methods</h3><div>A longitudinal cohort study followed 338 women with curable breast cancer, assessing QOL at baseline (before treatment), 3 months, 6 months, 12 months, and 24 months post-treatment. The FACT-B provided total and subscale scores (Physical, Social, Emotional, Functional, and Breast-specific well-being).</div></div><div><h3>Results</h3><div>Of 338 patients, 63 (18.64%) completed all assessments up to 24 months, and 68 (20.12%) completed up to 12 months. QOL decreased significantly at 3 months post-treatment (mean 74.98 vs. 85.6 at baseline, <em>p</em> < 0.001), remained below baseline at 6 months (79.34, p < 0.001), returned to baseline by 12 months (87.94, <em>p</em> = 0.147), and improved significantly by 24 months (110.92, p < 0.001). Physical and Functional well-being showed early declines, Social and Emotional well-being remained stable or improved, and Breast-specific well-being remained low, reflecting body image concerns.</div></div><div><h3>Conclusion</h3><div>The U-shaped QOL trajectory highlights the need for interventions at 3–6 months post-treatment, particularly for body image and physical function. These findings provide a foundation for targeted supportive care in Indian breast cancer survivors.</div></div>","PeriodicalId":50074,"journal":{"name":"Journal of Psychosomatic Research","volume":"203 ","pages":"Article 112551"},"PeriodicalIF":3.3,"publicationDate":"2026-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146068365","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-20DOI: 10.1016/j.jpsychores.2026.112545
Oscar Royuela , Francesco Oliva , Joana Bucker , Cristina De Córdoba Gil , Marta Fontana-McNally , Daniela L. Gatto , Daniel Guinart , Hernando Knobel-Freud , Pablo Knobel , Walter Lupo , Cristina Macias , Mila Montero , Ana Moreno-Alcázar , Johannes Wolf , Frank Padberg , Benedikt L. Amann , Alicia Valiente-Gómez , Bridget Hogg
Background
People living with human immunodeficiency virus (HIV; PLWH) can perceive aspects of the disease as traumatic. Objectives: 1) This study examined the trauma profile and sociodemographic and clinical correlates of HIV-related trauma; 2) to compare the impact of a post-traumatic stress disorder (PTSD) on clinical variables and biological markers in PLWH with HIV-related trauma; 3) to investigate the factors associated with PTSD; 4) to examine the relationship between childhood maltreatment, dissociation, and psychopathology.
Methods
93 Hospital del Mar Barcelona outpatient adults living with HIV with HIV-related trauma were included in this cross-sectional study. Participants were assessed with validated scales for PTSD, trauma, psychopathology, quality of life, functionality, and HIV-related stigma. CD4/CD8 ratio was also collected. PLWH with and without PTSD were compared in terms of clinical and sociodemographic factors and a pathway analysis was conducted.
Results
PLWH with PTSD reported significantly more anxious, depressive, and general psychiatric symptoms, poorer health-related quality of life and more stigma related to HIV compared to those with trauma symptoms only (all p < 0.0024). Age (OR = 1.08, p = 0.045) and previous psychiatric disorder (OR = 15.57, p = 0.010) can predict a PTSD diagnosis. PLWH with PTSD showed stronger correlations between childhood maltreatment, dissociation, and psychiatric symptoms than those with trauma symptoms only.
Conclusions
PTSD is associated with more psychiatric symptoms, lower quality of life and increased HIV-related stigma. Dissociation and PTSD were identified as a potential mechanism linking childhood maltreatment and mental health outcomes, suggesting a target for intervention. These findings support the need for PTSD screening and trauma-focused treatments in HIV care settings.
人类免疫缺陷病毒(HIV; PLWH)感染者可以将该疾病的某些方面视为创伤性疾病。目的:1)本研究探讨了hiv相关创伤的创伤概况、社会人口学和临床相关因素;2)比较创伤后应激障碍(PTSD)对hiv相关创伤PLWH患者临床指标和生物学指标的影响;3)探讨PTSD的相关因素;4)研究童年虐待、精神分离和精神病理之间的关系。方法对巴塞罗那德尔玛医院门诊的93例HIV相关创伤患者进行了横断面研究。用PTSD、创伤、精神病理、生活质量、功能和hiv相关污名的有效量表对参与者进行评估。同时采集CD4/CD8比值。比较合并与不合并PTSD的PLWH患者的临床及社会人口学因素,并进行通路分析。结果与仅有创伤症状的患者相比,患有PTSD的splwh患者报告的焦虑、抑郁和一般精神症状明显更多,健康相关生活质量更差,与HIV相关的耻辱感更多(p < 0.0024)。年龄(OR = 1.08, p = 0.045)和既往精神障碍(OR = 15.57, p = 0.010)可以预测PTSD的诊断。与仅有创伤症状的患者相比,患有PTSD的PLWH在儿童期虐待、精神分离和精神症状之间表现出更强的相关性。结论sptsd患者存在较多的精神症状、较低的生活质量和hiv相关的耻辱感。分离和创伤后应激障碍被确定为联系儿童虐待和心理健康结果的潜在机制,提出了干预的目标。这些发现支持在HIV护理环境中进行创伤后应激障碍筛查和以创伤为重点的治疗的必要性。
{"title":"Stressful life events, PTSD symptoms and mental health in people living with HIV","authors":"Oscar Royuela , Francesco Oliva , Joana Bucker , Cristina De Córdoba Gil , Marta Fontana-McNally , Daniela L. Gatto , Daniel Guinart , Hernando Knobel-Freud , Pablo Knobel , Walter Lupo , Cristina Macias , Mila Montero , Ana Moreno-Alcázar , Johannes Wolf , Frank Padberg , Benedikt L. Amann , Alicia Valiente-Gómez , Bridget Hogg","doi":"10.1016/j.jpsychores.2026.112545","DOIUrl":"10.1016/j.jpsychores.2026.112545","url":null,"abstract":"<div><h3>Background</h3><div><strong>People living with human immunodeficiency virus (HIV; PLWH) can perceive aspects of the disease as traumatic. Objectives:</strong> 1) This study examined the trauma profile and sociodemographic and clinical correlates of HIV-related trauma; 2) to compare the impact of a post-traumatic stress disorder (PTSD) on clinical variables and biological markers in PLWH with HIV-related trauma; 3) to investigate the factors associated with PTSD; 4) to examine the relationship between childhood maltreatment, dissociation, and psychopathology.</div></div><div><h3>Methods</h3><div>93 Hospital del Mar Barcelona outpatient adults living with HIV with HIV-related trauma were included in this cross-sectional study. Participants were assessed with validated scales for PTSD, trauma, psychopathology, quality of life, functionality, and HIV-related stigma. CD4/CD8 ratio was also collected. PLWH with and without PTSD were compared in terms of clinical and sociodemographic factors and a pathway analysis was conducted.</div></div><div><h3>Results</h3><div>PLWH with PTSD reported significantly more anxious, depressive, and general psychiatric symptoms, poorer health-related quality of life and more stigma related to HIV compared to those with trauma symptoms only (all <em>p</em> < 0.0024). Age (OR = 1.08, <em>p</em> = 0.045) and previous psychiatric disorder (OR = 15.57, <em>p</em> = 0.010) can predict a PTSD diagnosis. PLWH with PTSD showed stronger correlations between childhood maltreatment, dissociation, and psychiatric symptoms than those with trauma symptoms only.</div></div><div><h3>Conclusions</h3><div>PTSD is associated with more psychiatric symptoms, lower quality of life and increased HIV-related stigma. Dissociation and PTSD were identified as a potential mechanism linking childhood maltreatment and mental health outcomes, suggesting a target for intervention. These findings support the need for PTSD screening and trauma-focused treatments in HIV care settings.</div></div>","PeriodicalId":50074,"journal":{"name":"Journal of Psychosomatic Research","volume":"204 ","pages":"Article 112545"},"PeriodicalIF":3.3,"publicationDate":"2026-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146193009","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-20DOI: 10.1016/j.jpsychores.2026.112550
Caoimhe Mcloughlin , Neil Ramsay , Lineke Tak , Alan Carson , Jon Stone
Background
Stigma in Functional Neurological Disorder has been consistently reported by patient organisations as one of their biggest challenges. We aimed to longitudinally evaluate different components of stigma, namely perceived, internalised (self) and anticipated stigma experienced by patients with FND, and to explore associated factors.
Methods
Participants were mainly recruited prospectively via outpatient clinics at two centres, shortly after communicating the diagnosis. Measures included: perceived, internalised and anticipated stigma, somatic symptom burden, quality of life, depression, anxiety, illness attribution, and experience of care.
Results
Ninety-six respondents completed the baseline survey, of which 80 completed the follow-up (mean duration 7 months). Perceived stigma (Stigma Scale for Chronic Illness-8, mean 21.2) scores were in the moderate range. Regarding internalised stigma, 32% agreed they had considered that FND was their fault. Anticipated stigma was experienced most from work, followed by healthcare, then friends and family. Participants held a balanced view of their condition as physical and psychological in contrast to their perception of others' understanding of FND as psychological – which in turn significantly related to higher stigma scores. Identifying as a man, being in a relationship, higher age and level of education were statistically significantly protective against stigma. At follow up, perceived, self, and anticipated stigma, somatic symptom burden, quality of life, anxiety and depression scores did not change significantly.
Conclusion
People with FND experience high levels of perceived, self and anticipated stigma, and have high rates of physical and psychological comorbidity, which, in this cohort, did not improve over time. Counter-stigma approaches need to consider these different sources of stigma, outside just healthcare professionals.
{"title":"Stigma in functional neurological disorder; a longitudinal study","authors":"Caoimhe Mcloughlin , Neil Ramsay , Lineke Tak , Alan Carson , Jon Stone","doi":"10.1016/j.jpsychores.2026.112550","DOIUrl":"10.1016/j.jpsychores.2026.112550","url":null,"abstract":"<div><h3>Background</h3><div>Stigma in Functional Neurological Disorder has been consistently reported by patient organisations as one of their biggest challenges. We aimed to longitudinally evaluate different components of stigma, namely perceived, internalised (self) and anticipated stigma experienced by patients with FND, and to explore associated factors.</div></div><div><h3>Methods</h3><div>Participants were mainly recruited prospectively via outpatient clinics at two centres, shortly after communicating the diagnosis. Measures included: perceived, internalised and anticipated stigma, somatic symptom burden, quality of life, depression, anxiety, illness attribution, and experience of care.</div></div><div><h3>Results</h3><div>Ninety-six respondents completed the baseline survey, of which 80 completed the follow-up (mean duration 7 months). Perceived stigma (Stigma Scale for Chronic Illness-8, mean 21.2) scores were in the moderate range. Regarding internalised stigma, 32% agreed they had considered that FND was their fault. Anticipated stigma was experienced most from work, followed by healthcare, then friends and family. Participants held a balanced view of their condition as physical and psychological in contrast to their perception of <em>others'</em> understanding of FND as psychological – which in turn significantly related to higher stigma scores. Identifying as a man, being in a relationship, higher age and level of education were statistically significantly protective against stigma. At follow up, perceived, self, and anticipated stigma, somatic symptom burden, quality of life, anxiety and depression scores did not change significantly.</div></div><div><h3>Conclusion</h3><div>People with FND experience high levels of perceived, self and anticipated stigma, and have high rates of physical and psychological comorbidity, which, in this cohort, did not improve over time. Counter-stigma approaches need to consider these different sources of stigma, outside just healthcare professionals.</div></div>","PeriodicalId":50074,"journal":{"name":"Journal of Psychosomatic Research","volume":"203 ","pages":"Article 112550"},"PeriodicalIF":3.3,"publicationDate":"2026-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146025728","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-20DOI: 10.1016/j.jpsychores.2026.112548
T C Olde Hartman, L M Tak, D J C Hanssen
Persistent somatic symptoms (PSS) are common in primary care and often associated with functional impairment, dissatisfaction with medical care, and high societal costs. In the Netherlands, a strong primary care system has provided fertile ground for the development of a comprehensive approach to PSS, including evidence-based guidelines, stepped care pathways, and national patient information resources. This Editorial describes how PSS care is organized in the Dutch health system, the evolution of terminology and clinical concepts, the role of coordinators of PSS care in primary, secondary, and tertiary care, and the integration of psychosomatic interventions within this care. We highlight system innovations such as Thuisarts.nl (i.e. GPinfo.nl), a national, evidence-based patient information platform aligned with Dutch general practice guidelines, national care standards and regional collaborative care networks, reflect on implementation challenges, and describe the Dutch approach. The Dutch experience illustrates that PSS care can be coherently organized when anchored in general practice and supported by national guidance, patient information, psychosomatic and allied interventions, and collaborative networks. Remaining challenges include embedding consultation skills in training, ensuring equitable access, measuring patient-valued outcomes, and aligning system incentives to sustain implementation.
{"title":"Persistent somatic symptoms in the Dutch healthcare system.","authors":"T C Olde Hartman, L M Tak, D J C Hanssen","doi":"10.1016/j.jpsychores.2026.112548","DOIUrl":"https://doi.org/10.1016/j.jpsychores.2026.112548","url":null,"abstract":"<p><p>Persistent somatic symptoms (PSS) are common in primary care and often associated with functional impairment, dissatisfaction with medical care, and high societal costs. In the Netherlands, a strong primary care system has provided fertile ground for the development of a comprehensive approach to PSS, including evidence-based guidelines, stepped care pathways, and national patient information resources. This Editorial describes how PSS care is organized in the Dutch health system, the evolution of terminology and clinical concepts, the role of coordinators of PSS care in primary, secondary, and tertiary care, and the integration of psychosomatic interventions within this care. We highlight system innovations such as Thuisarts.nl (i.e. GPinfo.nl), a national, evidence-based patient information platform aligned with Dutch general practice guidelines, national care standards and regional collaborative care networks, reflect on implementation challenges, and describe the Dutch approach. The Dutch experience illustrates that PSS care can be coherently organized when anchored in general practice and supported by national guidance, patient information, psychosomatic and allied interventions, and collaborative networks. Remaining challenges include embedding consultation skills in training, ensuring equitable access, measuring patient-valued outcomes, and aligning system incentives to sustain implementation.</p>","PeriodicalId":50074,"journal":{"name":"Journal of Psychosomatic Research","volume":" ","pages":"112548"},"PeriodicalIF":3.3,"publicationDate":"2026-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146047308","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}