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Clinical, Cosmetic and Investigational Dermatology logoLink to Clinical, Cosmetic and Investigational Dermatology
. 2021 Aug 3;14:971–980. doi: 10.2147/CCID.S322963

Location, Spreading and Oral Corticosteroids are Associated with Insomnia in Vitiligo Patients: A Case–Control Study

Jia-Wei Liu 1, Yan Tan 1, Tian Chen 1, Wei Liu 1, Yue-Tong Qian 1, Dong-Lai Ma 1,
PMCID: PMC8349229  PMID: 34377005

Abstract

Background

Vitiligo can cause disfiguration, impair the social function of the patients and induce physiological burdens. However, limited research about the health-related quality of life has been conducted in vitiligo patients’ sleeping conditions.

Objective

To evaluate the prevalence, severity, and risk factors of insomnia in vitiligo patients.

Methods

This case–control study was performed in March 2021. An online survey questionnaire including baseline information and the sleep-related instrument was sent to 762 vitiligo patients. The vitiligo-related evaluation was conducted by online video interview. According to whether having insomnia or not, patients were grouped and compared their clinical and demographic characteristics. The logistic regression model was conducted to analyze the risk factors for insomnia.

Results

A total of 409 patients were included. About 49.9% of patients (204/409) experienced insomnia. About 55.9% (114/204) of the insomnia in vitiligo patients was adjustment sleep disorder caused by vitiligo. Development, aggravation, or recurrence of vitiligo were deemed as the first reason for insomnia in 71.1% of the sample (81/114). There were significant differences in age (32.1±4.1 vs 27.9±4.2 years, P < 0.001), the percentage of female (62.8% vs 49.3%, P=0.006) and working in the urban areas (77.0% vs 66.3%, P = 0.017), vitiligo in face and neck (67.2% vs 48.8%, P < 0.001), progression in vitiligo (65.7% vs 49.3%, P=0.001), oral corticosteroids (25.0% vs 16.6%, P=0.036) and depression (5.4% vs 0.5%, P = 0.003) between groups. After adjusting for gender, age and comorbidity, the multivariate logistic regression revealed that vitiligo in face and neck (OR=2.62; P=0.032), progression in vitiligo (OR=2.50; P=0.002), and oral corticosteroids (OR=2.71; P=0.021) remained risk factors for insomnia in vitiligo patients.

Conclusion

Insomnia is prevalent in vitiligo patients. Dermatologists should identify this condition carefully, especially humanistic factors in social life, and perform individualized “non-drug” treatment.

Keywords: vitiligo, sleep disorder, insomnia, risk factors, insomnia severity index, psychodermatology

Introduction

Insomnia is becoming a more prominent public health problem in recent society and causes a social-economic burden.1 The annual prevalence of insomnia disorder ranges from 12% to 20% in the adult population.1 The onset of insomnia is often triggered by a specific life event, including losing a job or getting a disease, resulting in impairment of daytime function and distressful emotion.2

Vitiligo is the most common depigmentation dermatosis, affecting 0.5% to 2.0% of the global population.3 The disease can cause disfiguration, impair the social function of the patients and induce physiological burdens. The autoimmune hypothesis is widely accepted as the etiopathogenesis of vitiligo.4 Vitiligo is associated with various autoimmune diseases, such as autoimmune thyroid disease, alopecia areata, and type 1 diabetes mellitus.5 Moreover, physiological disorders show a higher prevalence in vitiligo patients compared with normal population, including depression, stress, and insomnia.6,7 In the meantime, various autoimmune diseases are associated with sleep disorders.8 Patients with sleep disorders may suffer the potential risk for vitiligo.9 Therefore, a bidirectional relationship exists between vitiligo and sleep disorders. The onset of vitiligo may be a causal trigger of sleeping disorders, while sleeping disorder may also induce or further aggravate vitiligo. Limited research about the health-related quality of life has been conducted in the sleeping condition of vitiligo patients. In this study, We conducted a telemedicine survey on insomnia in vitiligo patients through mobile phones. The study aims to evaluate the prevalence, severity, and risk factors of insomnia in vitiligo patients.

Methods

Patients

This case–control study was performed in March 2021. The study’s research protocol was reviewed and approved by the Ethics Committee of the author’s affiliation (Ethical No: S-K1587) following the Declaration of Helsinki. All participants were informed about the purpose and used tools of this research, and patients’ written consents were obtained.

A total of 762 vitiligo patients who were under the follow-up by Prof. Ma were randomly picked from a pool of 3000 follow-up patients. Patients were excluded if he or she: (1) was under 18-year-old, (2) was not willing to participate in this study, (3) did not respond to the questionnaire before the deadline, (4) did not provide valid data, (5) was not willing to participate the online video interview, (6) did not understand the questions in the lists due to cognitive impairment or failure to recall the sleep-related details during the onset of vitiligo, (7) had significant stressors or adverse life events such as bankruptcy, death of close relatives and severe earthquake, (8) had other categories of sleep disorders, such as obstructive sleep apnea syndrome, narcolepsy-cataplexy syndrome, circadian rhythm sleep disorders (eg, jet lag, shift work disorder, etc.), and parasomnias (eg, partial arousal disorders, REM behavior disorder, etc.). Finally, a total of 409 patients were included in this study. Demographic data and baseline information are detailed in Table 1.

Table 1.

Basic Information of the Included Patients

Clinical Parameters Values
Age (Years, Mean±SD) 30.0±4.5
Gender (Female, n [%]) 229 (56.0)
Education (≥Bachelor, n [%]) 215 (52.6)
Workplace (Urban, n [%]) 293 (71.6)
Smoking (n [%]) 40 (9.8)
Alcohol (n [%]) 74 (18.1)
Duration of vitiligo(≥3 years, n [%]) 199(48.7)
Area of vitiligo (VASI≥6%, n [%]) 34 (8.3)
Exposure area (Face and neck, n [%]) 237 (57.9)
Insomnia (n [%]) 204(49.9)
Progress of vitiligo
Progression 235(57.5)
Stability/Regression 174(42.5)
Treatments
Oral glucocorticoid 85 (20.8)
Glycyrrhiza 266 (65.0)
External ointment 319 (78.0)
Masking agent 29 (7.1)
Psoralen 33 (8.1)
Phototherapy 135 (33.0)
Comorbidity
Hypertension (n, %) 7 (1.7)
Cardiac diseases (n, %) 4 (1.0)
Diabetes mellitus (n, %) 4 (1.0)
Hyperthyroidism (n, %) 31 (7.6)
Depression (n, %) 12 (2.9)

Procedure

We designed an online survey questionnaire that included the baseline information and a 45-item sleep-related instrument. The questionnaire was sent to the vitiligo patients through a social network application (WeChat). All the enrolled patients were invited to have an online video interview about the assessment of involved area and spreading of vitiligo lesion, using the instrument of Vitiligo Disease Activity (VIDA) and Vitiligo Area Scoring Index (VASI). The flow chart of this study is shown in Figure 1.

Figure 1.

Figure 1

The flow chart of this study.

Instruments

Vitiligo-Related Evaluation

VIDA score was used to evaluate vitiligo activity by online video interview. It is a six-point scale based on the patient’s report about disease activity. VIDA score was graded as follows: disease progression (expansion of existing lesions or appearance of new lesions) in 6 weeks or less, +4; disease progression in 6 weeks to 3 months, +3; disease progression in 3–6 months, +2; disease progression in 6–12 months, +1; stable for 1 year or more, +0; stable with spontaneous repigmentation for 1 year or more, −1.10

Involved area of vitiligo was assessed by VASI on the online video interview. VASI = ∑ [HAND UNITS] × [RESIDUAL DEPIGMENTATION].11

Insomnia-Related Evaluation

The sleep-related instrument mainly included five parts: 1. The insomnia diagnosis, 2. The Insomnia Severity Index, 3. The specific insomnia type, 4. Instruments and history requisition to exclude other sleep disorders, 5. Specific disturbance factors.

Among various sleep disorders, only insomnia was investigated in the present study. Insomnia was diagnosed according to the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-V). Patients were asked about their forepassed sleep condition, including whether they are satisfied, whether they felt having trouble sleeping associated with impairment to daytime functioning or well-being, whether sleep inadequacy occurred three or more nights per week, and whether the sleep disturbance was associated with vitiligo.

Patients who reported inadequate sleep would fill the Insomnia Severity Index (ISI), a brief, reliable, validated self-reporting instrument that yields a quantitative index of perceived insomnia severity. The indicator is composed of 7 items. Sleep disturbance severity, sleep dissatisfaction, and the degree of daytime functional impairment, impairment perception and distress, and distress related to the sleeping problem were assessed. A final score higher than 8 is identified as having insomnia. A higher score means more severe insomnia.12

Besides, structured questions were asked to confirm the specific insomnia type: difficulty initiating sleep, difficulty in maintaining sleep, early morning wake up, or nonrestorative sleep.

Other sleep disorders such as obstructive sleep apnea, restless leg, circadian rhythm sleep disorders, narcolepsy, and parasomnias were ruled out by relative screening instruments (International restless legs scale, StopBANG sleep apnea questionnaire) and history inquiry (Did you fall asleep in the daytime at the “wrong occasion” and “wrong location?”; Did you have recurrent severe nightmares or dream walk?).

The following 8 subtypes of insomnia are recognized by ICSD-2.13

Adjustment insomnia. This refers to insomnia that is triggered or aggravated by an identifiable stressor (vitiligo in the present study).

Psychophysiological insomnia. This insomnia subtype is characterized by heightened arousal and learned sleep-preventing associations such as trying too hard to fall asleep or excessive worrying about sleep.

Insomnia due to mental disorder. This subtype can be diagnosed when patients having a definitive diagnosed mental disorder and insomnia constitute an unusually predominant portion of symptoms in the underlying mental disorder or when insomnia warrants independent, clinical attention.

Inadequate sleep hygiene. This type of insomnia is caused by habitual activities that result in poor sleep, including excessive daytime napping, caffeine or alcohol intake before bedtime, excessively stimulating activities close to bedtime, etc.

Idiopathic insomnia. This is a form of chronic insomnia that started in infancy or childhood, has no identifiable precipitant, and is chronic and relentless, with no periods of sustained remission. An imbalance in the neurological/neurochemical sleep/wake system has been postulated.

Insomnia due to a medical condition. This is involved when a condition such as asthma or chronic heart failure can lead to insomnia.

Insomnia due to drugs or substances. This indicates that insomnia is based on the use of or withdrawal from prescription or recreational drugs, or it may be caused by food items or toxins such as carbon monoxide poisoning.

Physiological (organic) insomnia, unspecified. This is the category to use when insomnia does not fit into any of the insomnias mentioned before or when there is insufficiency of evidence to classify the patient into any of the above disorders.

Statistical Analysis

Data were analyzed using SPSS version 22 (IBM Corp., Armonk, NY, USA). Continuous variables were demonstrated as mean ± standard deviation (SD) and ordinal variables as proportions. Student’s t-test was performed to test the differences between groups in continuous variables, while Fisher exact test or Pearson chi-square test in ordinal variables. The Pearson correlation coefficient (coefficient, r) or Spearman’s rank correlation (coefficient, rho) was performed to determine the correlation between ISI score and VASI and between ISI score and VIDA score controlling the parameters with a correlation value of more than 0.5. The univariate logistic regression analysis was used to investigate the risk factors by calculating the odds ratio (OR) and 95% confidence interval (CI). The significant variables in the univariate logistic regression were included in multivariate analysis after adjusting the confounding factors. The cut-off points of the power analysis and statistical significance were p-value≤0.8 and 0.05, respectively.

Result

About 56.0% of the included patients were women, and the mean (±SD) age of the sample was 30.0 (±4.5) years. Table 1 shows their clinical and demographic characteristics. About 49.9% of patients (204/409) had an inadequate sleep, and 8.3% (17/204) used sleeping pills regularly.

The prevalence of difficulty in falling asleep, difficulty in staying asleep, non-restorative sleep, and too early awakening that occurred 3 days per week was 65.2%, 63.2%, 47.5%, and 37.2%, respectively.

Subtypes of Insomnia

About 87.3% of the sample (178/204) was deemed primary insomnias, while 12.7% was secondary insomnias. About 55.9% (114/204) of insomnia in vitiligo was adjustment sleep disorder as the first reason, followed by psychophysiological insomnia (13.7%, 28/204) and insomnia (8.3%, 17/204) due to mental disorder. Specific makeup is shown in Table 2.

Table 2.

Incidence of Subtypes of Insomnia

Insomnias Number and Percentage of Patients (n [%])
Primary insomnias
Adjustment sleep disorder 114 (55.9)
Psychophysiological insomnia 28 (13.7)
Insomnia due to mental disorder 17 (8.3)
Inadequate sleep hygiene 13(6.4)
Idiopathic insomnia 6 (2.9)
Total percentage 178 (87.3)
Secondary insomnias
Insomnia due to medical condition 14 (6.9)
Insomnia due to drug or substance 5 (2.5)
Physiological (organic) insomnia 4 (2.0)
Others (such as lactation, ambient noise) 3 (1.5)
Total percentage 26 (12.7)

Specific Analysis for the Vitiligo-Related Insomnia

Several factors can result in sleep disturbance in insomnia in vitiligo patients. The specific order of precedence of the results in response to “please list the factors discounting your sleep quality” was shown in Table 3.

Table 3.

Specific Analysis for the Vitiligo-Related Insomnia (Adjustment Sleep Disorder)

Factors Number and Percentage of Patients (n [%]) Examples
Development, aggravation, or recurrence of vitiligo 81 (71.1) Concern about the development, aggravation or reoccur of vitiligo, which may result in constant nightmares
Appearance 77 (67.5) Physiologically devastating of disfigurement caused by vitiligo which makes them have a singular appearance
Working/campus life 55 (48.2) Experienced discriminative or unpleasant event due to vitiligo in working or campus life
Fertility problems 54 (47.4) Concern about the inheritance tendency of vitiligo, hesitate about childbearing
Non-working/ recreational activities 45 (39.5) Feel embarrassed when changing clothes or expose affected body areas during non-working activities
Financial burden 42 (36.8) Medical expenses including medicines, camouflage cosmetics, and traffic expenses, etc
Side effects from vitiligo-related drugs 32 (28.1) Worry about other side-effect caused by steroid such as weight gain, or acne eruption;
Marital relationship or other intimate relationship 31 (27.2) Vitiligo affect intimate relationship, such as discounted sexual intercourse in marriage bonds, loss of confidence in front of their children

Among the vitiligo patients with the adjustment sleep disorder, development, aggravation, or recurrence of vitiligo was deemed as the first reasons for primary insomnia in 71.1% of the sample (81/114), followed by appearance (67.5%, 77/114) and working/campus life (48.2%, 55/114).

Comparisons Between Insomnia Patients and Non-Insomnia Patients with Vitiligo

There were significant differences in age (32.1±4.1 vs 27.9±4.2 years, P < 0.001), the percentage of female (62.8% vs 49.3%, P = 0.006) and working in the urban areas (77.0% vs 66.3%, P = 0.017), vitiligo in face and neck (67.2% vs 48.8%, P < 0.001), progression in vitiligo (65.7% vs 49.3%, P = 0.001), oral corticosteroids (25.0% vs 16.6%, P = 0.036) and depression (5.4% vs 0.5%, P = 0.003) between groups (Table 4).

Table 4.

Comparisons Between Insomnia Patients and Non-Insomnia Patients in Vitiligo

Clinical Parameters Insomnia Patients (n=204) Non-Insomnia Patients (n=205) P value
Age (Years) 32.1±4.1 27.9±4.2 <0.001*
Gender (Female, n [%]) 128 (62.8) 101 (49.3) 0.006*
Education (≥Bachelor, n [%]) 97 (47.5) 118 (57.6) 0.851
Workplace (Urban, n [%]) 157 (77.0) 136 (66.3) 0.017*
Smoking (n [%]) 24 (11.8) 16 (7.8) 0.120
Alcohol (n [%]) 42 (20.6) 32 (15.6) 0.191
Duration of vitiligo (≥3 years, n [%]) 101(49.5) 98(47.8) 0.806
Area of vitiligo (VASI≥6% , n [%]) 19 (9.3) 15(7.3) 0.581
Exposure area (Face and neck, n [%]) 137 (67.2) 100 (48.8) <0.001*
Progress of vitiligo
Progression 134(65.7) 101(49.3) 0.001*
Stability/Regression 70(34.3) 104(50.7)
Treatments
Oral corticosteroids 51 (25.0) 34 (16.6) 0.036*
Glycyrrhiza 136 (66.7) 130 (63.4) 0.558
Topical steroid/calcineurin ointment 153 (75.0) 166 (81.0) 0.181
Camouflage agent 14 (6.9) 15 (7.3) 0.858
Psoralen 17 (8.3) 16 (7.8) 0.844
Phototherapy 71 (34.8) 64 (31.2) 0.441
Comorbidity
Hypertension (n, %) 2 (1.0) 5 (2.4) 0.255
Cardiac diseases (n, %) 3 (1.5) 1 (0.5) 0.313
Diabetes mellitus (n, %) 2 (1.0) 2 (1.0) 0.996
Hyperthyroidism (n, %) 14 (6.9) 17 (8.3) 0.585
Depression (n, %) 11 (5.4) 1 (0.5) 0.003*

Note: *Means significantly different between groups.

Risk Analysis for Insomnia Patients in Vitiligo

The univariable logistic regression demonstrated that age ≥30 years (OR=1.85; 95% CI:1.19–2.73; P=0.006), female (OR=1.52; 95% CI:1.00–2.31; P=0.048), vitiligo in face and neck (OR=2.32; 95% CI:1.76–2.87; P=0.012), progression in vitiligo (OR=2.10; 95% CI:1.23–2.92; P=0.023), oral corticosteroids (OR=2.41; 95% CI:1.65–3.03; P=0.013) and depression (OR=2.52; 95% CI:1.92–2.93; P=0.001) were risk factors for insomnia patients in vitiligo.

After adjusting for gender, age and comorbidity, the multivariate logistic regression revealed that vitiligo in face and neck (OR=2.62; 95% CI:2.03–3.17; P=0.032), progression in vitiligo (OR=2.50; 95% CI:1.62–3.31; P=0.002), and oral corticosteroids (OR=2.71; 95% CI:2.11–3.19; P=0.021) remained risk factors for insomnia patients in vitiligo (Table 5).

Table 5.

Analysis of Risk Factors for Vitiligo Patients with Insomnia

Variables Univariate Multivariate
OR (95% CI) P value OR# (95% CI) P value
Age (years)≥30 1.85(1.19–2.73) 0.006*
Female 1.52(1.00–2.31) 0.048*
Vitiligo in face and neck 2.32(1.76–2.87) 0.012* 2.62(2.03–3.17) 0.032*
Progression in vitiligo 2.10(1.23–2.92) 0.023* 2.50(1.62–3.31) 0.002*
Oral corticosteroids 2.41(1.65–3.03) 0.013* 2.71(2.11–3.19) 0.021*
Depression 2.52(1.92–2.93) 0.001*

Notes: *Indicates statistical significance; #adjusted for age, gender and comorbidity; Odds ratios, as well as 95% CIs, were shown.

Abbreviations: OR, odds ratio; CI, confidence interval.

Correlations Analysis

There was no significant correlation between ISI score and VASI (r=0.502, R2=0.25, P=0.32). But a significant correlation was identified between ISI score and VIDA score (rho=0.620, R2=0.38, P<0.01).

Discussion

Various studies have evaluated the association between sleep problems and dermatoses, such as atopic dermatitis and psoriasis.14–16 These disorders are closely related to either apparent symptoms such as itch and pain,17 or multiple comorbidities including obesity, metabolic syndrome, hypertension, diabetes, cardiovascular events, asthma, and psychiatric disorders, which can all affect the course of sleep.14,18 However, little attention has been paid to the relationship between vitiligo and inadequate sleep. As the most common depigmentation dermatosis, vitiligo causes disfiguration to impair the patients’ physiological well-being and results in negative emotions such as anxiety and depression, which may interfere with sleep.19 The present findings demonstrated that up to 49.9% of vitiligo patients (204/409) had inadequate sleep. 55.9% of the vitiligo patients with insomnia reported the adjustment sleep disorder resulting from the vitiligo. Therefore, vitiligo-induced insomnia is prevalent. After adjusting for gender, age and comorbidity, the multivariate logistic regression revealed that vitiligo in the face and neck (OR=2.62), progression in vitiligo (OR=2.50), and oral corticosteroids (OR=2.71) were the risk factors for insomnia in vitiligo patients.

To the best of our knowledge, how and why failing to sleep well in patients with vitiligo has never been conducted in a previous study. In 2008, Mouzas et al investigated the relationship between vitiligo and sleep disorders.20 However, this study focused specifically on parasomnias. Its findings showed that patients suffering from vitiligo reported a significantly higher occurrence of sleepwalking, nocturnal enuresis, night illusions, sleep terrors, and nightmares than that of the control group before the occurrence of the disease. The authors assumed that association might exist between parasomnias in early life and subsequent onset of vitiligo, and neural mechanisms involving monoaminergic systems (especially the serotoninergic one) might potentially play an important role in the pathological mechanism of vitiligo. In the present study, we ranked the main subtypes of insomnia in vitiligo patients and analyzed its causes. Among the vitiligo patients with insomnia, development, aggravation, or recurrence of vitiligo was deemed the first reason for primary insomnia, followed by appearance and working/campus life. These figures further supported the onset of vitiligo as a psychological stressor that resulted in insomnia. Besides, a percentage ranging from 36.8% to 47.4% reported the concern about the medical cost of treating this disease, limitation in recreational activities due to significant stigma and concern about the inheritance of vitiligo. Despite a lower incidence of reporting side effects from vitiligo-related drugs and marital relationships or other intimate relationships than other reasons, it is not rare. It remains to be paid attention to from dermatologists. Collectively, vitiligo is frequently associated with social stigma and stressors. As a chronic illness lasting several decades and even throughout an entire lifetime, the stress may accumulate and result in insomnia, finally compromising the normal circadian rhythms. Vandeputte et al revealed that patients with chronic sleep disorders are prone to depression.21 Numerous studies have demonstrated the depression adversely affecting the quality of life of patients with vitiligo.22–24 Given this, there is a vicious circle between vitiligo and depression. However, in such a pathological process, inadequate sleep is seemingly intermediate between vitiligo and depression. Of note, the difference between adjustment sleep disorder and psychophysiological insomnia should be clarified. The former has definite stressor, and the latter is a type of conditioned or learned insomnia that involves either the conditioning of sleep-preventing habits in which repeated impairing of sleeplessness and situational, temporal, or behavioral stimuli normally associated with sleep leads to conditional arousal that impairs sleep, or somatized tension believed to result from the internalization of psychological conflicts and excessive worrying about sleep, which are incompatible with sleep.25,26 Simply, both adjustment sleep disorder and psychophysiological insomnia appear to result from psychological factors. However, the former lies in vitiligo’s stress, but the latter is caused by excessive concentration on sleep problems. In comparison with the rest of insomnia such as those due to mental disorder (eg, bipolar disorder), inadequate sleep hygiene (eg, coffee or tea), with a lower incidence, the present figure strongly indicated that adjustment sleep disorder and psychophysiological insomnia, especially for the former one, vitiligo-induced insomnia, is a prevalent problem among patients with vitiligo.

Significant differences in age, the percentage of females working in the urban areas, vitiligo in face and neck, progression in vitiligo, oral corticosteroids, and depression between the two groups were found in the present findings. Moreno et al demonstrated female gender had a higher prevalence of sleep disorders.27 Sidani et al indicated gender differences in insomnia could be associated with women’s stress, expression of somatic symptoms, and interest in maintaining their health to meet multiple role demands.28 These elements, either isolated or combined, can compromise sleep quality. Besides, an experimental study demonstrated that sleep regulation in female mice was dementedly affected by hormonal variations associated with the estrous cycle caused by sex hormone.29 Nam et al found a significant association between sleep duration and menstrual cycle in female adolescents.30 This may help explain why female vitiligo patients reported insomnia more frequently. In this study, the vitiligo patients with insomnia were older in age compared to those without insomnia. This is consistent with previous studies.31,32 After adjusting for gender, age, and comorbidity, the multivariate logistic regression revealed that vitiligo in the face and neck and vitiligo progression were risk factors for insomnia in vitiligo patients. Even though vitiligo does not cause systemic symptoms, the effect vitiligo has on quality of life is similar to other skin diseases, such as psoriasis and atopic dermatitis.4 Its impact on quality of life is mainly associated with negative psychological influence, for example, reduced self-esteem, increased embarrassment. These elements negatively affect social or sexual relations, resulting in vitiligo-related isolation, discrimination, social stigma, and even suicidal ideation.33–36 These feelings, which become a barrier for campus life, seeking a job, and even marriage directly or indirectly, would constantly exist in patients with vitiligo and thus impaired sleep quality. As for oral corticosteroids, previous studies have demonstrated steroids reduced REM sleep and tended to enhance intermittent wakefulness.37,38 This may be related to the effect of corticosteroids on the function of pituitary-adrenal and pituitary-thyroid. Moreover, administration of oral steroids is usually associated with rapid disease progression in clinical practice.39 The disease exacerbation may cause physiological stress and subsequently result in insomnia.

The present study has demonstrated that insomnia was a prevalent condition in our sample. Seemingly, this sleep problem affected their quality of life by a psychopathological condition such as depression and stress. Therefore, it may be significant for dermatologists to have general identification of these conditions in vitiligo patients, both psychological and physical, and offer individualized therapy. Not only routine treatment but also the evaluation for the psychiatric status of patients with vitiligo, especially women and the elderly, should be considered. Besides, the interaction between the patient and the dermatologists is also crucial. In some cases with severe sleep problems, the psychiatrist–patients communication may be more significant. Papadopoulos et al demonstrated that effective counseling could contribute to improving self-esteem and quality of life in vitiligo patients and may even positively influence the course of this chronic condition.40 Till now, no relevant study has been conducted between insomnia treatment and vitiligo disease control. However, theoretically, improved sleep quality may have a positive influence on the disease course. Moreover, in patients with other comorbidities such as heart diseases treated with beta-blockers, treatment of insomnia can also ease the physiological burden, deactivate the hypothalamus-pituitary-adrenergic axis, decrease the excitability of the sympathetic nervous system, and result in better control of skin dermatosis and systemic disorders. From the psychological effect on sleep disorders, the patients’ quality of life can be significantly improved. Of note, different patients with vitiligo have specific worries about this disease and problems. Dermatologists should identify them carefully, especially humanistic factors in social life, and perform individualized “non-drug” treatment.

There are several limitations in this research. First, only insomnia was investigated. However, in addition to insomnia, the international classification of sleep disorders lists another seven categories of sleep disorders, such as obstructive sleep apnoea syndrome, narcolepsy-cataplexy syndrome, etc. Second, the evaluating method for a sleep disorder was subjective instead of objective methods such as polysomnography (PSG). This may not benefit the reliable conclusions. The detailed information about insomnia may be easily affected by the patient’s psychological factors such as cognitive processes and recall bias. A discrepancy between subjective reporting and objective assessments about the disrupted sleep exists. Especially considering the disease, with a course of a long slow continuous progress, parts of included patients with vitiligo failed to report the actual situation of insomnia when they just had the vitiligo. Thirdly, image clarity was limited by mobile phone camera resolution. Diminution of accuracy in VASI evaluation may exist during online interview. Last, the subtypes and reasons for insomnia in vitiligo patients in the present Tables 2 and 3 may not list the whole picture. We could neglect insidious ones behind this chronic disorder with complex psychological activities. These limitations open the door for the further study.

Conclusion

Vitiligo can cause disfiguration, impair the social function of the patients and induce physiological burdens. The present findings revealed that vitiligo in face and neck, progression in vitiligo, and oral corticosteroids were risk factors for insomnia in vitiligo patients. Therefore, insomnia is prevalent in vitiligo patients. Dermatologists should identify this condition carefully, especially humanistic factors in social life, and perform individualized “non-drug” treatment.

Acknowledgment

We would like to thank all patients involved in this study. The patients in this manuscript have given written informed consent to publication of their case details.

Funding Statement

The article had no funding source.

Disclosure

All authors report no conflict of interest.

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