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Mental Health Associations With Vitiligo

The Mental Health Associations With Vitiligo: a Population-based Cohort Study in the UK

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04953338
Enrollment
36104
Registered
2021-07-07
Start date
2021-06-18
Completion date
2022-10-21
Last updated
2025-12-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adjustment Disorders, Anxiety Disorders, Depressive Episode, Overdose, Parasuicide, Recurrent Depressive Disorder, Self-Harm, Deliberate, Social Phobia, Substance Abuse, Suicide, Attempted, Vitiligo

Brief summary

This cohort study is a large population-based study in the UK to determine the risks of comorbid mental health conditions (including depression, anxiety and other potential psychological complications of vitiligo) in adults with vitiligo compared to controls and to evaluate whether the relative risks may vary by different ethnicity.

Detailed description

This study has two primary outcomes 1) Prevalence and incidence of mental health condtions in people diagnosed with vitiligo compared to matched controls and 2) Primary care and secondary healthcare utilisation in patients diagnosed with vitiligo and having a prevalent depressive conditon compared to matched controls. In addition, the study examines risk of time off work and unemployment in people diagnosed with vitiligo compared to matched controls.

Interventions

OTHERExposure of mental health condtion of interest

Common mental health conditions consist of depressive episodes, recurrent depressive disorder and anxiety disorder.

Sponsors

Pfizer
CollaboratorINDUSTRY
Momentum Data
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* All eligible adults ≥18 (as at date of vitiligo diagnosis for cases or start of follow-up for controls) registered with GP practices contributing data to OPCRD between January 1, 2004 and December 31, 2020, were eligible for inclusion in the study.

Exclusion criteria

* People with less than 1 year of follow up available

Design outcomes

Primary

MeasureTime frameDescription
Number of Participants With Depressive EpisodesAt the time of diagnosis in all people diagnosed with vitiligo 2004-2020 inclusive. For matched controls, the date of diagnosis of their matched case.Prevalence of common mental health conditions (depressive episodes) in adult people diagnosed with vitiligo and matched controls without vitiligo.
Risk of Depressive Episodes Within Adult Patients With VitiligoWithin two years of vitiligo diagnosis. For matched controls, within two years of the date of diagnosis of their matched case.Adjusted hazard ratio calculated using Cox proportional hazards models
Number of Participants With Anxiety DisorderAt the time of diagnosis in all people diagnosed with vitiligo 2004-2020 inclusive. For matched controls, the date of diagnosis of their matched case.Prevalence of common mental health conditions (Anxiety Disorder) in adult people diagnosed with vitiligo and matched controls without vitiligo.
Number of Participants With Recurrent Depressive DisorderAt the time of diagnosis in all people diagnosed with vitiligo 2004-2020 inclusive. For matched controls, the date of diagnosis of their matched case.Prevalence of common mental health conditions (Recurrent Depressive Disorder) in adult people diagnosed with vitiligo and matched controls without vitiligo.
Risk of Anxiety Disorder Within Adult Patients With VitiligoWithin two years of vitiligo diagnosis. For matched controls, within two years of the date of diagnosis of their matched case.Adjusted hazard ratio calclulated using Cox Proportional hazard models
Risk of Recurrent Depressive Disorder Within Adult Patients With VitilgoWithin two years of vitiligo diagnosis. For matched controls, within two years of the date of diagnosis of their matched case.Adjusted hazard ratio calculated using Cox proportional hazards models. Adjusted for age, gender, ethnicity, social deprivation quintile, body mass index, smoking status, alcohol use and comorbidities (hypertension, hyperlipidaemia, type 2 diabetes, atrial fibrillation, angina, myocardial infarction, heart failure, stroke, chronic kidney disease stages 3-5, chronic obstructive pulmonary disease, asthma, chronic liver disease and dementia).

Countries

United Kingdom

Participant flow

Participants by arm

ArmCount
Cases
Patients with a confirmed diagnosis of Vitiligo within the study period will be included as cases for analysis.
7,224
Controls
The controls will be defined by matching cases with people who have never been diagnosed with vitiligo either prior to or during the study period, by age and sex, at General Practice level.
28,880
Total36,104

Baseline characteristics

CharacteristicCasesControlsTotal
Age, Continuous44 years44 years44 years
Age, Customized
Age group, years
18-29
1377 Participants5534 Participants6911 Participants
Age, Customized
Age group, years
30-39
1526 Participants6087 Participants7613 Participants
Age, Customized
Age group, years
40-49
1463 Participants5822 Participants7285 Participants
Age, Customized
Age group, years
50-59
1251 Participants5006 Participants6257 Participants
Age, Customized
Age group, years
60-69
918 Participants3647 Participants4565 Participants
Age, Customized
Age group, years
70-76
534 Participants2155 Participants2689 Participants
Age, Customized
Age group, years
80+
155 Participants629 Participants784 Participants
Alcohol use, Categorical
Alcoholism
116 Participants499 Participants615 Participants
Alcohol use, Categorical
Excess use
970 Participants3604 Participants4574 Participants
Alcohol use, Categorical
Non-drinker
2438 Participants8984 Participants11422 Participants
Alcohol use, Categorical
Not recorded
901 Participants4692 Participants5593 Participants
Alcohol use, Categorical
Safe use
2799 Participants11101 Participants13900 Participants
Body Mass Index, Categorical
18.5-24.9 Healthy weight
2129 Participants7544 Participants9673 Participants
Body Mass Index, Categorical
<18.5 Underweight
174 Participants670 Participants844 Participants
Body Mass Index, Categorical
25-29.9 Overweight
2282 Participants8511 Participants10793 Participants
Body Mass Index, Categorical
30-34.9 Class I obesity
1080 Participants4316 Participants5396 Participants
Body Mass Index, Categorical
35-39.9 Class II obesity
367 Participants1674 Participants2041 Participants
Body Mass Index, Categorical
>40 Class III obesity
211 Participants1013 Participants1224 Participants
Body Mass Index, Categorical
Not recorded
981 Participants5152 Participants6133 Participants
Race/Ethnicity, Customized
Asian or Asian British
1060 Participants3200 Participants4260 Participants
Race/Ethnicity, Customized
Black, African, Caribbean or Black British
170 Participants556 Participants726 Participants
Race/Ethnicity, Customized
Missing
1966 Participants8769 Participants10735 Participants
Race/Ethnicity, Customized
Mixed
66 Participants238 Participants304 Participants
Race/Ethnicity, Customized
Not stated
199 Participants949 Participants1148 Participants
Race/Ethnicity, Customized
Other
259 Participants1155 Participants1414 Participants
Race/Ethnicity, Customized
White
3504 Participants14013 Participants17517 Participants
Sex: Female, Male
Female
3828 Participants15304 Participants19132 Participants
Sex: Female, Male
Male
3396 Participants13576 Participants16972 Participants
Smoking Status, Categorical
Current smoker
1147 Participants5881 Participants7028 Participants
Smoking Status, Categorical
Ex-smoker
3521 Participants12862 Participants16383 Participants
Smoking Status, Categorical
Non-smoker
2357 Participants8629 Participants10986 Participants
Smoking Status, Categorical
Not recorded
169 Participants1431 Participants1600 Participants
Smoking Status, Categorical
Passive smoker
30 Participants77 Participants107 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 00 / 0
other
Total, other adverse events
0 / 00 / 0
serious
Total, serious adverse events
0 / 00 / 0

Outcome results

Primary

Number of Participants With Anxiety Disorder

Prevalence of common mental health conditions (Anxiety Disorder) in adult people diagnosed with vitiligo and matched controls without vitiligo.

Time frame: At the time of diagnosis in all people diagnosed with vitiligo 2004-2020 inclusive. For matched controls, the date of diagnosis of their matched case.

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
CasesNumber of Participants With Anxiety Disorder569 Participants
ControlsNumber of Participants With Anxiety Disorder2031 Participants
Primary

Number of Participants With Depressive Episodes

Prevalence of common mental health conditions (depressive episodes) in adult people diagnosed with vitiligo and matched controls without vitiligo.

Time frame: At the time of diagnosis in all people diagnosed with vitiligo 2004-2020 inclusive. For matched controls, the date of diagnosis of their matched case.

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
CasesNumber of Participants With Depressive Episodes1018 Participants
ControlsNumber of Participants With Depressive Episodes4007 Participants
Primary

Number of Participants With Recurrent Depressive Disorder

Prevalence of common mental health conditions (Recurrent Depressive Disorder) in adult people diagnosed with vitiligo and matched controls without vitiligo.

Time frame: At the time of diagnosis in all people diagnosed with vitiligo 2004-2020 inclusive. For matched controls, the date of diagnosis of their matched case.

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
CasesNumber of Participants With Recurrent Depressive Disorder1093 Participants
ControlsNumber of Participants With Recurrent Depressive Disorder4305 Participants
Primary

Risk of Anxiety Disorder Within Adult Patients With Vitiligo

Adjusted hazard ratio calclulated using Cox Proportional hazard models

Time frame: Within two years of vitiligo diagnosis. For matched controls, within two years of the date of diagnosis of their matched case.

Population: Patients with a pre-existing diagnosis of anxiety disorder were excluded from the analysis

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
CasesRisk of Anxiety Disorder Within Adult Patients With Vitiligo122 Participants
ControlsRisk of Anxiety Disorder Within Adult Patients With Vitiligo382 Participants
95% CI: [1.01, 1.51]
Primary

Risk of Depressive Episodes Within Adult Patients With Vitiligo

Adjusted hazard ratio calculated using Cox proportional hazards models

Time frame: Within two years of vitiligo diagnosis. For matched controls, within two years of the date of diagnosis of their matched case.

Population: Patients with a pre-existing diagnosis of depressive episodes were excluded from this analysis

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
CasesRisk of Depressive Episodes Within Adult Patients With Vitiligo157 Participants
ControlsRisk of Depressive Episodes Within Adult Patients With Vitiligo501 Participants
95% CI: [0.92, 1.32]
Primary

Risk of Recurrent Depressive Disorder Within Adult Patients With Vitilgo

Adjusted hazard ratio calculated using Cox proportional hazards models. Adjusted for age, gender, ethnicity, social deprivation quintile, body mass index, smoking status, alcohol use and comorbidities (hypertension, hyperlipidaemia, type 2 diabetes, atrial fibrillation, angina, myocardial infarction, heart failure, stroke, chronic kidney disease stages 3-5, chronic obstructive pulmonary disease, asthma, chronic liver disease and dementia).

Time frame: Within two years of vitiligo diagnosis. For matched controls, within two years of the date of diagnosis of their matched case.

Population: Patients with a pre-existing diagnosis of recurrent depressive disorder were excluded from the analysis

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
CasesRisk of Recurrent Depressive Disorder Within Adult Patients With Vitilgo113 Participants
ControlsRisk of Recurrent Depressive Disorder Within Adult Patients With Vitilgo312 Participants
95% CI: [1.01, 1.56]

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026