Eleftheriadou, Viktoria
- Contact Information
Biography
Dr Viktoria Eleftheriadou is a Consultant Dermatologist and the Lead for the Vitiligo Clinical And Research Centre (Vitiligo CARE) for adult and paediatric patients at Walsall Healthcare & The Royal Wolverhampton NHS Trusts. Vitiligo CARE is a unique, national vitiligo research centre and centre of excellence in the heart of Midlands, where both research trials on innovative treatments for vitiligo is being conducted and treatments recommended by the BAD offered to patients under one roof. The centre offers opportunities to ...
Biography
Dr Viktoria Eleftheriadou is a Consultant Dermatologist and the Lead for the Vitiligo Clinical And Research Centre (Vitiligo CARE) for adult and paediatric patients at Walsall Healthcare & The Royal Wolverhampton NHS Trusts. Vitiligo CARE is a unique, national vitiligo research centre and centre of excellence in the heart of Midlands, where both research trials on innovative treatments for vitiligo is being conducted and treatments recommended by the BAD offered to patients under one roof. The centre offers opportunities to Dermatology Specialty Trainees, nurses and other healthcare professionals to get involved in national and international research projects and will increase participation in NIHR portfolio. Viktoria’s research interests include pigmentary disorders, eczema, vitiligo, phototherapy, evidence-based dermatology, trials methodology, outcome measures and qualitative research. She completed her PhD at the Centre of Evidence Based Dermatology, University of Nottingham, which was NIHR funded and was awarded in 2013. Dr Eleftheriadou holds the following relevant roles: • Honorary Associate Professor with Institute of Applied Health Research of the University of Birmingham. • Section Editor for the British Journal of Dermatology, one of the top 3 Dermatology journals in the world. • Lead author for British Association of Dermatologists (BAD) guidelines for the management of vitiligo (2021). She has presented her work at national and international conferences and received invitations from the American Academy of Dermatology (AAD) and the European Academy of Dermatology and Venereology (EADV) to present her work at AAD and EADV Annual meetings. She frequently delivers lectures to Consultant Dermatologists, Associate Specialists in Dermatology and GPs. Currently, she is working on several national and international projects including an international observational study and registry for vitiligo patients (adults and children) (VIRTUAL-GLOBAL) and an international consensus on the definitions of the severity and relapses in vitiligo (INTERCEPT project). She is also the UK Chief Investigator for several trials and studies.
- Fields of Specialization
- Dermatology
- Degrees
- MD, MRCP(UK), SCE(Derm), PhD
- Departments
- Dermatology
- ORCID
- 0000-0001-5776-1466
- Position / Title
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Consultant Dermatologist and Associate Professor
- Current research programs / themes
- Pigmentary disorders, vitiligo, paediatric dermatology, general dermatology, eczema, alopecia, JAK inhibitors
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Estimating the burden of vitiligo : a systematic review and modelling studyAkl, Jennifer; Lee, Solam; Ju, Hyun Jeong; Parisi, Rosa; Kim, Ji Yoon; Jeon, Jae Joon; Heo, Yeon-Woo; Eleftheriadou, Viktoria; Hamzavi, Iltefat; Griffiths, Christopher E M; et al. (Elsevier, 2024-06)Background: Vitiligo is a chronic autoimmune disease characterised by depigmented skin patches, which can pose substantial psychosocial challenges particularly in individuals with dark skin tones. Despite its impact on quality of life, there is an absence of standardised global epidemiological data. We sought to address this gap with the present study. Methods: In this study we did a systematic review and modelling analysis to estimate the global, regional, and national prevalence and incidence of vitiligo. We did a comprehensive search of nine digital libraries (PubMed, Embase, Web of Science, Scientific Electronic Library Online, KCI Korean Journal Database, Russian Science Citation Index, Western Pacific Region Index Medicus, Informit, and Health Research and Development Information Network) from inception up to May 25, 2023. We included cross-sectional or cohort studies reporting the incidence rate or prevalence of vitiligo, or data from which incidence rate or prevalence could be calculated, in the general population of a country or area of a country. Summary estimate data were extracted. A main outcome was to estimate the worldwide, regional, and country-specific lifetime prevalence of vitiligo diagnosed by physicians or dermatologists among the general population and in adults and children (as per age groups defined in included studies). We used a Bayesian hierarchical linear mixed model to estimate prevalence, and calculated number of affected individuals using the UN population structure in 2022. In estimating lifetime prevalence, studies reporting point or period prevalence were excluded. Our other main outcome was to estimate incidence rates of vitiligo, but due to a small number of studies, the data on incidence were presented in a descriptive summary. This study was registered on PROSPERO, CRD42023390433. Findings: Our search identified 22 192 records, of which 90 studies met our inclusion criteria. Of these studies, six focused on the incidence of vitiligo, 79 reported on the prevalence of vitiligo, and five provided data on both incidence and prevalence. 71 studies reported on lifetime prevalence. In the most recent years studied, incidence rates in the general population ranged from 24·7 cases (95% CI 24·3-25·2) per 100 000 person-years in South Korea in 2019, to 61·0 cases (60·6-61·4) in the USA in 2017. In individual studies, incidence rates showed an increasing trend over the periods studied. The global lifetime prevalence of vitiligo diagnosed by a physician or dermatologist was estimated at 0·36% (95% credible interval [CrI] 0·24-0·54) in the general population (28·5 million people [95% CrI 18·9-42·6]), 0·67% (0·43-1·07) in the adult population (37·1 million adults [23·9-58·9]), and 0·24% (0·16-0·37) in the child population (5·8 million children [3·8-8·9]). Vitiligo prevalence was higher in adults than in children across all regions. Central Europe and south Asia reported the highest prevalence (0·52% [0·28-1·07] and 0·52% [0·33-0·82], respectively, in the general population). Interpretation: This study highlights the need for standardised epidemiological data collection globally to inform public health policies and improve vitiligo diagnosis and management. Emphasis on the impact on individuals with darker skin tones is crucial to reducing stigma and improving quality of life. Furthermore, our study highlights the need to conduct more research in regions and populations that have been historically under-represented, to effectively address the worldwide burden of vitiligo.
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Assessing and managing mental health of people with vitiligo : UK-wide consultation exerciseBarlow, Richard; Ahmed, Alia; Fellows, Jodie; Goulding, Jon; Handley, Kelly; Schneider, Alex; Thompson, Andrew; Valente, Marie; Waters, Cerith; Eleftheriadou, Viktoria; et al. (Oxford University Press, 2023-12-19)No abstract available
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Risk of melanoma and nonmelanoma skin cancer in people with vitiligo : United Kingdom population-based cohort studyFerguson, John; Eleftheriadou, Viktoria; Nesnas, John; Eleftheriadou, Viktoria; Dermatology; Medical and Dental; Guys Hospital; Walsall Healthcare NHS Trust; Pfizer (Elsevier, 2023-11)Although genetic studies have found an inverse relationship between vitiligo and skin cancer, epidemiological evidence is conflicting. We investigated the risk of skin cancer in adults with vitiligo using United Kingdom electronic primary care records from the Optimum Patient Care Research Database 2010-2020. Vitiligo cases were age, sex, and general practitioner practice matched to population controls without vitiligo. Incidence of melanoma, nonmelanoma skin cancers (squamous cell carcinoma and basal cell carcinoma), and actinic keratoses was compared between vitiligo cases and controls using Cox regression. A total of 15,156 vitiligo cases were matched to 60,615 controls. Vitiligo was associated with a 38% reduced risk of new-onset skin cancer (adjusted hazard ratio [aHR] = 0.62, 95% confidence interval [CI] = 0.52-0.75, P < 0.001) and skin cancer subtypes; melanoma (aHR = 0.39, 95% CI = 0.23-0.65, P < 0.001), squamous cell carcinoma (aHR = 0.67, 95% CI = 0.49-0.90, P < 0.01), basal cell carcinoma (aHR = 0.65, 95% CI = 0.51-0.83, P < 0.001). There was no significant association for actinic keratosis (aHR = 0.88, 95% CI = 0.77-1.01). People with vitiligo have a markedly reduced incidence of melanoma and nonmelanoma skin cancer. Given concerns that some treatments, such as phototherapy, may increase skin cancer risk, this finding provides reassurance to people with vitiligo and clinicians managing the condition.
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Facial involvement is reflective of patients' global perception of vitiligo extentMerhi, Samar; Salameh, Pascale; Abboud, Mounya; Seneschal, Julien; Eleftheriadou, Viktoria; Pane, Isabelle; Tran, Viet-Thi; Shourick, Jason; Ezzedine, Khaled; Eleftheriadou, Viktoria; et al. (Oxford University Press, 2023-07)Background: The involvement of visible areas in vitiligo has been found to be correlated with increased psychiatric morbidity. Although multiple tools have been developed to assess vitiligo, no cutoff for improvement or worsening of vitiligo from a patient's perspective has been established. Objectives: To determine the minimal clinically important difference (MCID) of the Self-Assessment Vitiligo Extent Score (SA-VES) in patients with vitiligo and to evaluate, from the patient's perspective, the importance of the change in the involvement of visible areas (face and hands) in patients' overall perception of disease worsening or improving. Methods: This was a cross-sectional study in the context of the ComPaRe e-cohort. Adult patients with vitiligo were invited to answer online questionnaires. They completed the SA-VES twice, 1 year apart. In addition, patients answered a 5-point Likert anchor question aimed at assessing their perception of the evolution of the extent of their vitiligo. The MCID was calculated using distribution- and anchor-based approaches. Using ordinal logistic regression, the change of vitiliginous lesions on the face or hands was compared to the overall extent of vitiligo (patches on all body areas). Results: In total, 244 patients with vitiligo were included in the analyses; 20 (8%) were found to have an improvement in their vitiligo. The MCID in worsened patients was equal to a 1.3% body surface area [95% confidence interval (CI) 1.01-1.43] increase in the SA-VES. For participants with improved vitiligo, the MCID was equal to a decrease in total SA-VES of 1.3% (95% CI 0.867-1.697). Patients' perceptions of change in their vitiligo was increased sevenfold when it affected the face vs. the rest of the body. Conclusions: Changes in the facial SA-VES were highly correlated with patients' impressions of the extent of vitiligo.
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The mental health associations of vitiligo : UK population-based cohort studyThompson, Andrew R.; Eleftheriadou, Viktoria; Nesnas, John; Eleftheriadou, Viktoria; Dermatology; Medical and Dental; Cardiff University; Walsall Healthcare NHS Trust; Pfizer Ltd (Cambridge University Press, 2022-10)Background: Vitiligo is an acquired, autoimmune depigmenting skin disorder that may affect psychological well-being. Aims: To determine the risk and impact of psychological comorbidity in people with new-onset vitiligo. Method: We conducted a retrospective observational study, using UK general practice data (2004-2020). Adults diagnosed with vitiligo (n = 7224) were matched 1:4 with controls (n = 28 880). Associations within 2 years of diagnosis were assessed for psychological conditions: recurrent depressive disorder (RDD), depressive episodes, non-phobia-related anxiety disorder, social phobia, adjustment disorder, substance misuse, self-harm and suicide attempts. Healthcare utilisation, time off work and unemployment within 1 year were compared in those with and without a mental health condition at vitiligo diagnosis. Results: At diagnosis, people with vitiligo had a similar prevalence of mental health conditions as controls, except for anxiety disorder (cases 7.9%, controls 7.0%; P = 0.014). Incident RDD and anxiety disorder were more common in people with vitiligo (RDD: adjusted hazard ratio (aHR) 1.25, 95% CI 1.01-1.55; anxiety disorder: aHR 1.23, 95% CI 1.00-1.51). Risk was highest in Black and minority ethnic individuals (RDD: aHR 1.72, 95% CI 1.06-2.79; depressive episodes: aHR 1.56, 95% CI 1.03-2.37). No association was found with other mental health conditions. People with vitiligo and psychological comorbidity had more primary care encounters, more time off work and higher unemployment. Conclusions: People with vitiligo have a higher incidence of RDD and anxiety disorder than controls, and this risk increase may be greatest in Black and minority ethnic populations.
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Prescribing and using vitiligo treatments : lessons from a nested process evaluation within the HI-Light vitiligo randomized controlled trialLeighton, Paul; Chalmers, Joanne R; Batchelor, Jonathan M; Rogers, Andy; Akram, Perways; Haines, Rachel H; Meakin, Garry D; White, Jennifer; Ravenscroft, Jane C; Sach, Tracey H; et al. (Oxford University Press, 2022-05-30)Background: The HI-Light Trial demonstrated that for active, limited vitiligo, combination treatment with potent topical corticosteroid (TCS) and handheld narrowband ultraviolet B offers a better treatment response than potent TCS alone. However, it is unclear how to implement these findings. Aim: We sought to answer three questions: (i) Can combination treatment be used safely and effectively by people with vitiligo?; (ii) Should combination treatment be made available as routine clinical care?; and (iii) Can combination treatment be integrated within current healthcare provision? Methods: This was a mixed-methods process evaluation, including semi-structured interviews with a purposive sample of trial participants, structured interviews with commissioners, and an online survey and focus groups with trial staff. Transcripts were coded by framework analysis, with thematic development by multiple researchers. Results: Participants found individual treatments easy to use, but the combination treatment was complicated and required nurse support. Both participants and site investigators felt that combination treatment should be made available, although commissioners were less certain. There was support for the development of services offering combination treatment, although this might not be prioritized above treatment for other conditions. A 'mixed economy' model was suggested, involving patients purchasing their own devices, although concerns regarding the safe use of treatments mean that training, monitoring and ongoing support are essential. The need for medical physics support may mean that a regional service is more practical. Conclusion: Combination treatment should be made available for people seeking treatment for vitiligo, but services require partnership with medical physics and ongoing training and support for patients.