S Torabi1, M Mozdourian2, R Rezazadeh2, A Payandeh3, S Badiee4, E Darchini-Maragheh1. 1. Cutaneous Leishmaniasis Research Center, Mashhad University of Medical Sciences, Mashhad, Iran. 2. Lung Diseases Research Center, Mashhad University of Medical Sciences, Mashhad, Iran. 3. Community Nursing Research Center, Zahedan University of Medical Sciences, Zahedan, Iran. 4. Department of complementary and Chinese medicine, School of Persian complementary medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Nothing to disclose.To the Editor,The ongoing outbreak of COVID‐19 has posed significant threats to international health. The first biologic step of potential infectivity of COVID‐19 is the priming of the spike proteins by transmembrane protease, serine 2 (TMPRSS2). TMPRSS2 cleave angiotensin converting enzyme 2 for augmented viral entry and thus is regarded as essential for viral spread and pathogenesis in the infected hosts.
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Androgen receptor activity is considered as a requirement for the transcription of the TMPRSS2 gene and no other regulatory element of the TMPRSS2 promoter has been described in human to date.
Thus, this led us to hypothesize that variations in the androgen receptor gene may predispose male COVID‐19 patients to increased disease severity.Through a prospective study, 116 hospitalized patients due to severe COVID‐19 infection (confirmed with viral nucleic acid testing) were involved in the study. Lung high‐resolution computed tomography (HRCT) findings as well as laboratory data, and disease outcome including discharge, intensive care unit (ICU) care, intubation and death, were recorded for each patient. hyper‐androgenic skin manifestations including androgenetic alopecia (AGA), acne severity, seborrheic dermatitis and hirsutism were examined by a dermatologist. Severity of AGA was assessed using Hamilton scale and Ludwig scale for male and female patients, respectively. Patients with immunosuppressive conditions and anti‐androgenic medication were excluded. Analyses were carried out by Statistical Package for Social Sciences computer software (SPSS version 16, Chicago, IL, USA).Totally, 118 confirmed COVID‐19 patients including 61 men (51.7%) and 57 women (48.3%) with mean age of 60.45 ± 15.99 (ranging 18–100) years were investigated. All the patients were symptomatic. Triad of dyspnoea, cough and fatigue were the most common symptoms that were recorded in 100 (84.7%), 78 (66.1%) and 57 (48.3%) patients, respectively. Twenty‐nine patients (24.4%) had all the symptoms of the triad (Table 1).
Table 1
Demographic characteristics, clinical history, symptoms and signs of 118 patients admitted to hospitals with confirmed COVID‐19 infection
Demographic characteristics, clinical history, symptoms and signs of 118 patients admitted to hospitals with confirmed COVID‐19 infectionResults (Mean ± SD)N (%)Results (Mean ± SD)N (%)Results (Mean ± SD)N (%)Results (Mean ± SD)N (%)Percutaneous O2 saturation (%)˃90Chest HRCT showed abnormalities in 115 patients (97.4%) whom all of them had more than one involved lobe. Lesions were inclined to distribute in the lower lobes. Right inferior (92.3%) and right middle lobes (61.0%) were the most and the least affected lobes, respectively. Combination of ground glass opacification and consolidation which was presented in 65 patients (55.1%) was the most involved pattern.Androgenetic alopecia was present in 45 men out of 61 (73.7%) including 13 (28.8%) severe AGA (Hamilton scale >5), 22 (48.8%), moderate AGA (Hamilton scale 3–4) and 10 (22.2%) mild AGA (Hamilton scale 1–2). In total, 32 women out of 57 (56.1%) had AGA including 2 (6.2%) severe AGA (Ludwig score advanced and frontal), 14 (43.7%) moderate AGA (Ludwig score 2–3) and 16 (50.0%) mild AGA (Ludwig score 1). Both the mortality rate and AGA severity were significantly higher in patients over 60 years old (P = 0.003 and 0.020, respectively). AGA was significantly higher in men than women (P = 0.045). AGA severity did not show any significant correlation with HRCT severity, neither with patients’ ICU care, intubation and expire in both genders. Similarly, other hyper‐androgenic manifestations did not significantly correlate with disease outcome and HRCT severity (Table 2).
Table 2
Lung HRCT findings vs. hyper‐androgenic finding in 118 patients admitted to hospitals with confirmed COVID‐19 infection
HRCT findings
N (%)
Hyper‐androgenic findings
N (%)
Number of involved lobes (˃5%)
Both genders (N = 118)
0
3 (2.5%)
History of acne
18 (15.3%)
1
0 (0.0%)
2
16 (13.6%)
Current acne
7 (5.9%)
3
21 (17.8%)
Mild
3 (2.5%)
4
31 (26.3%)
Moderate
4 (3.4%)
5
47 (39.8)
Severe
0 (0.0%)
Lobe of lesion distribution (˃5%)
History of greasy skin
38 (32.2%)
Left upper lobe
90 (76.2%)
Left lower lobe
105 (8.9%)
Right upper lobe
78 (66.1%)
Current greasy skin
23 (19.5%)
Right middle lobe
72 (61.0%)
Right lower lobe
109 (92.3%)
History of seborrheic dermatitis
20 (16.9%)
Bilateral upper lobes
70 (59.3%)
Bilateral lower lobes
99 (83.9%)
Pattern of the lesion
Current seborrheic dermatitis
6 (5.1%)
Ground glass opacification
30 (25.4%)
Male (N = 61)
Consolidation
2 (1.7%)
Androgenic alopecia
(Hamilton‐Norwood scale)
45 (73.7%)
Crazy paving
1 (0.8%)
Mild
10 (22.2%)
Ground glass and Consolidation
65 (55.1%)
Moderate
22 (48.8%)
All the three patterns
20 (16.9%)
Severe
13 (28.8%)
Excess hair
24 (39.3%)
Face
21 (87.5%)
Ear
23 (95.8%)
Chest
6 (25.0%)
Pleural effusion
21 (17.8%)
Pre‐puberty
0 (0.0%)
Pericardial effusion
1 (0.8%)
Female (N = 57)
Cavitation
0 (0.0%)
Androgenic alopecia
(Ludwig scale)
32 (56.1%)
Mild
16 (50.0%)
Moderate
14 (43.7%)
Severe
2 (6.2%)
History of infertility
2 (3.5%)
Dysmenorrhea
11 (19.3%)
History of hirsutism
15 (26.3%)
Current hirsutism
19 (33.3%)
Face
17 (89.4%)
Nipple
9 (47.3%)
Lung HRCT findings vs. hyper‐androgenic finding in 118 patients admitted to hospitals with confirmed COVID‐19 infectionAndrogenic alopecia(Hamilton‐Norwood scale)45 (73.7%)Androgenic alopecia(Ludwig scale)Among disease outcomes, ICU care, intubation and death were recorded in 48 patients (40.7%), 16 (13.6%) and 22 (18.6%) patients, respectively. Mortality rate was 18.0% among males (11 patients) and 19.3% among women (11 patients). No significant difference was observed between the two genders in terms of disease outcome.The precise prevalence of AGA among healthy Iranian population is unknown; however, based on literature, prevalence of age‐matched AGA in a similar white population is estimated 31–53% in men and up to 38% in women.
Our results indicated substantial proportion of AGA in hospitalized COVID‐19 patients considering estimated age‐matched AGA in healthy population. Moreover, hyper‐androgenic phenotypes have been recently observed by some authors to have correlation with severe forms of COVID‐19.
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However, the results of this study revealed that AGA as well as other skin hyper‐androgenic manifestations are not related risk of severe COVID‐19 infection. Additional large‐scale prospective studies are recommended.
Funding source
The study was financially supported by the Vice Chancellor for Research, Mashhad University of Medical Sciences, Mashhad, Iran.
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