Literature DB >> 27541601

Socioeconomic and sociocultural determinants of psychological distress and quality of life among patients with psoriasis in a selected multi-ethnic Malaysian population.

Zhenli Kwan1,2, Yii Bonn Bong3, Leng Leng Tan1, Shu Xian Lim1, Adrian Sze Wai Yong1, Chin Chwen Ch'ng1, Maw Pin Tan4, Suganthi Thevarajah5, Rokiah Ismail6.   

Abstract

Patients with psoriasis may have increased risk of psychological comorbidities. This cross-sectional study aimed at determining associations between sociocultural and socioeconomic factors with the Depression Anxiety Stress Scale (DASS) scores and the Dermatology Life Quality Index (DLQI) scores. Adult patients with psoriasis were recruited from a Dermatology outpatient clinic via convenience sampling. Interviews were conducted regarding socio-demographic factors and willing subjects were requested to complete the DASS and DLQI questionnaires. The Pearson χ2 test, Fisher's exact test and multivariate logistic regression were used for statistical analysis to determine independent predictors of depression, anxiety, stress and severe impairment of quality of life. Unadjusted analysis revealed that depression was associated with Indian ethnicity (p = .041) and severe impairment of quality of life was associated with Indian ethnicity (p = .032), higher education (p = .013), higher income (p = .042), and employment status (p = .014). Multivariate analysis revealed that Indian ethnicity was a predictor of depression (p = .024). For stress, tertiary level of education (p = .020) was an independent risk factor while a higher monthly income was a protective factor (p = .042). The ethnic Indians and Malays were significantly more likely than the ethnic Chinese to suffer reduced quality of life (p = .001 and p = .006 respectively) and subjects with tertiary education were more likely to have severe impairment of quality of life (p = .002). Our study was unique in determining sociocultural influences on psychological complications of psoriasis in a South East Asian population. This has provided invaluable insight into factors predictive of adverse effects of psoriasis on psychological distress and quality of life in our patient population. Future studies should devise interventions to specifically target at risk groups in the development of strategies to reduce morbidity associated with psoriasis.

Entities:  

Keywords:  Psoriasis; culture; psychology; quality of life; socioeconomic factors

Mesh:

Year:  2016        PMID: 27541601     DOI: 10.1080/13548506.2016.1220603

Source DB:  PubMed          Journal:  Psychol Health Med        ISSN: 1354-8506            Impact factor:   2.423


  10 in total

1.  Depression and anxiety among patients with psoriasis: A correlation with quality of life and associated factors.

Authors:  Raishan S Bakar; Sharifah Z S Jaapar; Afiq F Azmi; Yeoh C Aun
Journal:  J Taibah Univ Med Sci       Date:  2021-03-16

2.  Prevalence and Odds of Anxiety Disorders and Anxiety Symptoms in Children and Adults with Psoriasis: Systematic Review and Meta-analysis.

Authors:  Isabelle Jalenques; Fabien Bourlot; Elisa Martinez; Bruno Pereira; Michel D'Incan; Sophie Lauron; Fabien Rondepierre
Journal:  Acta Derm Venereol       Date:  2022-08-26       Impact factor: 3.875

Review 3.  Epidemiology of Psoriasis and Comorbid Diseases: A Narrative Review.

Authors:  Jin Bu; Ruilian Ding; Liangjia Zhou; Xiangming Chen; Erxia Shen
Journal:  Front Immunol       Date:  2022-06-10       Impact factor: 8.786

Review 4.  Dermatology: how to manage psoriasis and recognize differences in pathophysiology and presentation in patients with skin of colour.

Authors:  Yuliya Lytvyn; Muskaan Sachdeva; Asfandyar Mufti; Jensen Yeung
Journal:  Drugs Context       Date:  2022-05-31

5.  Electronic cigarette use and psychological distress in the Native Hawaiian and Pacific Islander adults compared with other racial/ethnic groups: Data from the National Health Interview Survey, 2014.

Authors:  Marie-R Narcisse; Page Dobbs; Christopher R Long; Rachel S Purvis; Kim S Kimminau; Pearl A McElfish
Journal:  J Community Psychol       Date:  2019-09-19

6.  Patient-Reported Disease Severity and Quality of Life Among Arabic Psoriatic Patients: A Cross-Sectional Survey.

Authors:  Moetaza Soliman
Journal:  Clin Cosmet Investig Dermatol       Date:  2020-08-25

7.  Psychosomatic Syndromes and Symptom Severity in Chronic Psoriasis.

Authors:  Annamaria Petito; Angela Piazzoli; Mario Altamura; Antonello Bellomo; Francesco Bernardini; Laura Scarponi; Piero Porcelli
Journal:  Clin Neuropsychiatry       Date:  2020-08

8.  Deucravacitinib in Moderate to Severe Psoriasis: Clinical and Quality-of-Life Outcomes in a Phase 2 Trial.

Authors:  Diamant Thaçi; Bruce Strober; Kenneth B Gordon; Peter Foley; Melinda Gooderham; Akimichi Morita; Kim A Papp; Lluís Puig; M Alan Menter; Matthew J Colombo; Yedid Elbez; Renata M Kisa; June Ye; Andrew A Napoli; Lan Wei; Subhashis Banerjee; Joseph F Merola; Alice B Gottlieb
Journal:  Dermatol Ther (Heidelb)       Date:  2022-01-13

9.  Acceptance of Illness, Satisfaction with Life, Sense of Stigmatization, and Quality of Life among People with Psoriasis: A Cross-Sectional Study.

Authors:  Beata Kowalewska; Mateusz Cybulski; Barbara Jankowiak; Elżbieta Krajewska-Kułak
Journal:  Dermatol Ther (Heidelb)       Date:  2020-03-19

Review 10.  The psychosocial adaptation of patients with skin disease: a scoping review.

Authors:  Xiu-Jie Zhang; Ai-Ping Wang; Tie-Ying Shi; Jun Zhang; Hui Xu; Da-Qiu Wang; Li Feng
Journal:  BMC Public Health       Date:  2019-10-29       Impact factor: 3.295

  10 in total

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