Electrocardiogram Findings in Patients with Alopecia Areata.

INTRODUCTION: While autoimmune comorbidities are common in alopecia areata, little is known about comorbid cardiovascular disease. The purpose of this study was to evaluate the incidence of bradyarrhythmia in patients with alopecia areata.
METHODS: Retrospective review of electrocardiograms of 124 patients with [Formula: see text] 50% scalp hair loss (severe alopecia areata) was conducted and compared to National Health and Nutrition Examination Survey (NHANES) data.
RESULTS: The prevalence of bradycardia in females with alopecia areata was 24.3% (95% CI, 14.5-34.1%) and in those age 40 years or older was 40.8% (95% CI, 22.2-53.5%) compared to 19.5% in the NHANES III population. The prevalence of bradycardia in males with alopecia areata was 36.0% (95% CI, 22.7-49.3%) and in those age 40 years or older was 50.0% (95% CI, 21.7-78.3%) compared to 26.9% in the NHANES III population.
CONCLUSION: The potential association between bradycardia and alopecia areata merits further investigation.

Key Summary Points

Introduction

Alopecia areata (AA) is an autoimmune disease characterized by non-scarring hair loss. Comorbid cardiovascular disease in patients with autoimmune disorders is an area of active investigation. In AA patients, higher levels of cardiac troponin I have been documented [1]. One recent study suggests AA patients are at an increased risk of acute myocardial infarction [2], while another study found elevated inflammatory and cardiovascular/atherosclerosis-related biomarkers in AA patients [3]. Previous work has not suggested a connection between AA and arrhythmias. We sought to quantify the prevalence of sinus bradycardia in AA patients.

Methods

This retrospective study involved AA patients who underwent stringent screening protocols, including electrocardiogram (ECG), for therapeutic clinical trials between October 2015 and January 2020 at two institutions with approval from both Yale institutional review board (HIC# 2000026876) and UCI institutional review board (HS# 2016-3076). Screening data included patients’ age, gender, severity of scalp hair loss [assessed by Severity of Alopecia Tool (SALT) score = % scalp hair loss], ECG findings, comorbidities, current medications, body mass index (BMI), and laboratory values. Bradycardia was defined as a heart rate 60 beats per minute (bpm). Findings were compared to ECG heart rate data from males and females in the general population (NHANES III 1988–1994) [4].

Statistical Analysis

Summary statistics were calculated as mean (standard deviation (SD)) for continuous variables and counts (%) for categorical variables. Two-sample Welch’s t-test was used to compare mean differences of continuous variables between patients with bradycardia and patients without bradycardia, while the chi-square test was used for assessing the association of bradycardia with categorical variables. Analyses were performed using the statistical software SAS version 9.4 (Cary, NC). A two-sided p-value < 0.05 was considered statistically significant.

Results

A total of 124 patients were included (Table 1). All patients had AA with SALT score 50 (i.e., 50% or more scalp hair loss). Of this cohort, 74 were female (59.7%). The mean (SD) age for all patients was 36.4 (15.4). The mean (SD) age for the NHANES III population was 57.0 (12.7), with all patients age 40 or older.

Table 1

Summary statistics of patient variables at the screening visit

	ECG HR ≥ 60(n = 88)	Bradycardia(ECG HR < 60)(n = 36)	Total(n = 124)	p value
Age (years)	34.8 (15.81)	40.3 (13.75)	36.4 (15.39)	0.07
SALT score at screen	84.6 (20.01)	82.4 (21.70)	83.9 (20.45)	0.58
Years since diagnosis	11.4 (9.53)	11.4 (9.75)	11.4 (9.56)	0.98
Duration of current episode of severe AA (years)	3.5 (4.03)	4.5 (4.00)	3.8 (4.03)	0.21
Systolic blood pressure	123 (12.32)	123 (15.15)	123 (13.15)	0.91
Diastolic blood pressure	78 (10.10)	79(10.71)	78 (10.24)	0.98
ECG heart rate	71 (9.66)	54 (4.91)	66 (11.57)	< 0.001
TSH (μIU/mL)	1.85 (0.94)	1.76 (1.07)	1.83 (0.98)	0.68
Height (cm)	163.5 (20.00)	169.8 (9.27)	165.3 (17.77)	0.021
Weight (kg)	81.0 (30.17)	73.3 (15.86)	78.8 (27.01)	0.07
Body mass index	26.9 (5.79)	25.3 (4.23)	26.5 (5.42)	0.09
Hemoglobin (g/dL)	14.13 (1.29)	14.16 (1.36)	14.14 (1.31)	0.91
Sex
Female	56 (63.64%)	18 (50.00%)	74 (59.68%)	0.16
Male	32 (36.36%)	18 (50.00%)	50 (40.32%)
Hypothyroidism
Yes	13 (15.12%)	6 (17.14%)	19 (15.70%)	0.78
No	73 (84.88%)	29 (82.86%)	102 (84.30%)
Levothyroxine
Yes	10 (11.76%)	5 (13.89%)	15 (12.40%)	0.77
No	75 (88.24%)	31 (86.11%)	106 (87.60%)
Beta blocker
Yes	4 (4.65%)	0 (0.00%)	4 (3.28%)	0.32
No	82 (95.35%)	36 (100.00%)	118 (96.72%)
Calcium channel blocker
Yes	2 (2.33%)	0 (0.00%)	2 (1.64%)	1.00
No	84 (97.67%)	36 (100.00%)	120 (98.36%)
Electrolytes normal
Yes	74 (86.05%)	30 (83.33%)	104 (85.25%)	0.70
No	12 (13.95%)	6 (16.67%)	18 (14.75%)
History of cardiovascular diseasea
Yes	7(8.14%)	2 (5.56%)	9 (7.38%)	1.00
No	79 (91.86%)	34 (94.44%)	113 (92.62%)

Data are presented as mean (SD), n (%)

AA alopecia areata, ECG electrocardiogram, HR heart rate, SALT Severity of Alopecia Tool, TSH thyroid-stimulating hormone

aCardiovascular disease included any of the following: hypertension, prior myocardial infarction, previous diagnosis of coronary artery disease, hyperlipidemia, or cardiac conduction abnormalities

The prevalence of sinus bradycardia in our cohort was 29.0% compared to 22.9% in the NHANES III population. The prevalence of bradycardia in females with AA was 24.3% (95% CI, 14.5–34.1%) and in those age 40 years or older was 40.8% (95% CI, 22.2–53.5%), compared to 19.5% in the NHANES III population. The prevalence of bradycardia in males with AA was 36.0% (95% CI, 22.7–49.3%) and in those age 40 years or older was 50.0% (95% CI, 21.7–78.3%), compared to 26.9% in the NHANES III population. In our cohort of patients with bradycardia, the mean (SD) HR was 53.6 bpm (4.91), and there was a trend toward higher mean age in those with bradycardia (40.3 vs. 34.8 years old; p = 0.07).

No association was found between bradycardia and blood pressure (p = 0.91), bradycardia and history of cardiovascular disease (p = 1.00), and bradycardia and hypothyroidism (p = 0.78). TSH values were similar in the two groups (1.76 vs. 1.85, p = 0.68) (Table 1). While BMI was slightly lower among bradycardic patients (25.29 vs. 26.93), this was not statistically significant (p = 0.09). No bradycardic patients were taking beta blockers or calcium channel blockers. Bradycardia was not associated with electrolyte abnormalities (p = 0.70) or anemia (p = 0.91).

Other ECG abnormalities were seen in 33 patients (37.5%) without bradycardia and 11 patients (30.6%) with bradycardia and included: early repolarization, ectopic premature complexes, incomplete right bundle branch block, intraventricular conduction delay, left axis devation, left ventricular hypertrophy, non-specific T-wave abnormality, premature atrial contractions, right atrial enlargement, right and left ventricular hypertrophy, sinus arrhythmia, short PR interval, ST elevation, right ventricular conduction delay, and premature ventricular contractions.

Discussion

Our data suggest there is an increased prevalence of sinus bradycardia in AA patients, reaching significance in female patients. This observation emerged from the relatively large number of patients with AA at our centers participating in therapeutic clinical trials. The fact that vital signs are rarely performed (and ECGs never) as part of routine dermatologic care may explain why this potentially novel finding has escaped notice.

Whereas sinus bradycardia suggests cardiovascular health in the general population, the clinical implications of this finding in AA patients is unknown and the mechanism underlying this association unclear. The lifetime prevalence of AA is 2% in the US population, and autoimmune and inflammatory comorbid diseases are common in patients with AA. Thyroid disorders including subclinical hypothyroidism, Graves’ disease, and Hashimoto’s are particularly common. While hypothyroidism may cause bradycardia, there was no association between a history of hypothyroidism and the presence of bradycardia in our cohort; furthermore, all patients in our cohort who had a diagnosis of hypothyroidism were adequately treated with thyroid replacement therapy and had normal TSH values at the time ECGs were performed. A common cause of slower HR is physical conditioning. While activity patterns of the AA cohort were not queried, BMI did not significantly differ between those with and without bradycardia, making differences in physical conditioning an unlikely explanation. Furthermore, in our experience AA patients do not differ significantly from the general population in terms of lifestyle, further arguing that fitness is unlikely to account for the differences between the AA cohort and the NHANES population.

There are a few possible mechanisms by which sinus bradycardia  could manifest in AA. Heart rate is determined by two factors—intrinsic sinus node function and autonomic activity. Inflammatory processes would be expected to increase sympathetic activity and decrease vagal activity, leading to increases in heart rate through autonomic influence on the sinus node; thus, autonomic influences would not explain our finding. Ischemia can lead to bradycardia, but we noted no ECG findings or symptoms suggestive of coronary artery disease in our patients.

Another explanation for sinus bradycardia in patients with AA could be fibrosis. Primary sinus node dysfunction is often caused by fibrosis, and, interestingly, cardiac remodeling and fibrosis have been found in murine models of AA, although conduction system or sinus node disease has not specifically been reported in these models [5, 6]. Higher levels of cardiac troponin I have been documented in patients with AA [1], and, in a murine model, an autoimmune response to cardiac troponin I induces cardiac inflammation and fibrosis [7, 8]. It is also possible that genes involved in development of sinus node fibrosis overlap with those that determine AA [9, 10].

Study Limitations

Our data were limited by a relatively small cohort of AA patients in a clinical trial setting with more females (59.7%), and the mean age of our cohort was 20 years younger than NHANES III, which collected ECG data only in patients age 40 and older. To our knowledge, there are no publicly available  ECG data in populations of similar age to our AA cohort. Lastly,  cardiac magnetic resonance imaging (MRI) was not performed as part of this study.

Conclusion

In summary, our data suggest there is increased prevalence of sinus bradycardia in AA patients. Further investigation of the prevalence and mechanism of bradycardia in AA patients is warranted.

Why carry out this study?

While autoimmune comorbidities are common in alopecia areata (AA), little is known about comorbid cardiovascular disease.

The purpose of this study was to evaluate the incidence of bradycardia in patients with AA.

What was learned from the study?

Our data suggest there is increased prevalence of sinus bradycardia in AA patients.

Further investigation of the prevalence of bradycardia and its relationship to cardiovascular disease in AA patients is warranted.