Abstact
Background
Coronavirus disease (COVID-19) currently named SARS-CoV-2 is a contagious disease caused by a coronavirus; incompatible data are present on the possible relationship among COVID-19 vaccines and hair loss.
Aims
The objective of the current study was to assess dermoscopically the prevalence of hair loss among an Egyptian population following COVID-19 vaccination.
Methods
A total of 2000 participants were enrolled in this cross-sectional study. Adult males and females who received one of recognized COVID-19 vaccine were included, irrespective of the status of previous COVID-19 infection. Those who were aged less than 18 years or above 60 years were excluded. Furthermore, subjects self-reporting hair loss were assessed by dermoscopy.
Results
Among the studied cases, n = 478 (23.9%) complained of hair loss following vaccination. The majority of cases noticed their hair loss during the first 2 months post-vaccination (n = 215 after the first month and n = 158 after the 2nd month respectively).
Conclusion
We reported prevalence of post-vaccination hair fall that was confirmed by trichoscopy and which affected approximately one quarter of participants who received COVID-19 vaccines. Other factors, such as stress and infection, cannot be excluded and remain to be further investigated by larger multicenter studies.
Keywords: Alopecia, Telogen effluvium, Trichoscopy
Background
A number of skin conditions and reactions have been reported after COVID-19 vaccinations. A number of skin local reactions such as swelling, induration, redness, and pruritis as well as injection site pain and tenderness were among the commonly observed following vaccinations. Other reported manifestations included acute type I hypersensitivity reactions such as angioedema, urticaria, and anaphylaxis as well as delayed type IV hypersensitivity reactions and autoimmune-mediated cutaneous lesions such as vasculitis [1].
Hair loss accompanying (COVID-19) infection as well as its various vaccine strains has been of much concern. No clear understanding of the mechanism behind vaccine-related hair loss had been explained; however, a number of factors were hypothesized [2]. COVID-19-infected individuals had been more prone to microthrombi formation that caused compromise of the vascular circulation within scalp hair follicles [2].
Dermoscopy is a tool that is able to magnify anatomic and morphologic structures not clear enough to the naked eyes. Within hair follicles, dermoscopy allows better visualization of perifollicular and inter follicular patterns as well as alteration in hair shaft thickness and density.
Trichoscopy utilizes dermoscope for diagnosing and assessing hair disorders and was first used as a term in 2006. The hand-held, in-office easy to use tool allows for rapid non-invasive assessment of inflammatory hair disorders [3].
The objective of the current study was to assess dermoscopically the prevalence of hair loss among an Egyptian population following COVID-19 vaccination.
Methods
This was a multicenter, cross-sectional study conducted from January 2022 till January of 2023. A total 2030 participants attending dermatology clinics at university as well as ministry of health hospitals were included in the study after their consenting. Adult males and females who received one of recognized COVID-19 vaccine were included, irrespective of the status of previous COVID-19 infection. Those who were aged less than 20 years or above 60 years were excluded. Out of the 2030 participants who were primarily included, 30 subjects were later excluded leaving 2000 participants for data analysis. Exclusions were for lack of evident COVID-19 vaccination certification or for failure to show up following agreement to participate.
All participants were subjected to
Data collection using a questionnaire covering the following characteristics: age, gender, hair fall before and after COVID-19 vaccines, type of vaccine, previous history of COVID-19 infection, and preexisting conditions that might be related to hair fall. A pilot study was conducted on 20 volunteers to ensure clarity and convenience of the questions and to estimate the time needed to fill the questionnaire. No identifier or sensitive data were collected. Those complaining of hair loss were subjected to complete general and local hair examination using trichoscopy to confirm hair loss. Dermoscopic evaluation (DermLite DL4) and imaging were reproduced at baseline, 3 months, and 6 months for follow-up.
The study was conducted in accordance with the Declaration of Helsinki and upon approval by the Local Ethical Committee—Al Azhar University N: 000084. Statistical analysis using continuous variables was presented as mean ± SD (standard deviation) for parametric data and median (min–max) for non-parametric data. Qualitative data were described using number and percent. Association between categorical variables was tested using chi-square test. For all statistical tests, p-value > 0.05 was considered not significant and p-value < 0.05 was considered significant. All data were analyzed using IBM SPSS Statistics for Windows, Version 26, and Microsoft Excel 365.
Results
The mean age of studied population was 30.77(± 7.54 SD) with range 21–54 years. No age significance was demonstrated between males and females p = 0.74. Among the studied cases, there were 524 who received Astra Zeneca vaccine; of whom 248 cases (47.3%) were females and 276 cases (52.7%) were males. Of the 32 cases who received Johnson and Johnson vaccine, 8 cases (25.0%) were females and 24 cases (75.0%) were males. Sixty-eight (68) subjects reported receiving Pfizer-BioNTech COVID-19 vaccine and twelve (12) received Moderna COVID-19 vaccine. Among all participants, 23.8% (n = 476) received Sinopharm vaccine and among them 200 were males and 276 were females. Sinovac and Sputnik vaccines were administered by 416 and 380 cases respectively. Of all 2000 cases reported in this study, 92 confirmed vaccination with Sputnik Light vaccine, among which 13 were females and 79 were males. Among included subjects, 98% (n = 1960) were not diagnosed with COVID-19, while only 40 cases (2%) reported positive infection with COVID-19.
Among the studied cases, n = 478 (23.9%) complained of hair loss following vaccination. The majority of cases noticed their hair loss during the first 2 months post-vaccination (n = 215 after the first month and n = 158 after the 2nd month respectively) (Tables 1 and 2). Of the 478 cases complaining of hair loss, 389 of them presented with acute onset telogen effluvium (TE), 13 reported acute exacerbations of their androgenetic alopecia, 40 presented with new onset alopecia areata, and 20 experienced recurrences in preciously treated alopecia areata (Tables 2, 3, 4, and 5).
Table 1.
Vaccine | Study group (n = 2000) | P-value | ||
---|---|---|---|---|
Number | Female | Male | ||
AstraZeneca | n = 524 | 248 (47.3%) | 276 (52.7%) | |
Johnson and Johnson | n = 32 | 8 (25%) | 24 (75%) | |
Moderna | n = 12 | 1 (8.3%) | 11 (91.7%) | |
Pfizer | n = 68 | 12 (17.6%) | 56 (82.4%) | X2 = 96.11 |
Sinopharm | n = 476 | 200 (42%) | 276 (58%) | P-value < 0.001 |
Sinovac | n = 416 | 144 (34.6%) | 272 (65.4%) | |
Sputnik | n = 380 | 208 (54.7%) | 172 (45.3%) | |
Sputnik light | n = 92 | 13 (14.1%) | 79 (85.9%) |
X2: chi-square test. P-value < 0.05 is considered significant
Table 2.
Vaccine | Hair loss | Study group (n = 2000) | P-value | |
---|---|---|---|---|
Frequency | Percent | |||
AstraZeneca n = 524 |
No | 360 | 68.7% | |
Yes | 164 | 31.3% | ||
Johnson and Johnson n = 32 |
No | 28 | 87.5% | |
Yes | 4 | 12.5% | ||
Moderna n = 12 |
No | 10 | 83.3% | |
Yes | 2 | 16.7% | ||
Pfizer n = 68 |
No | 56 | 82.4% | |
Yes | 12 | 17.6% | X2 = 28.42 | |
Sinopharm n = 476 |
No | 360 | 75.6% | P < 0.001 |
Yes | 116 | 24.4% | ||
Sinovac n = 416 |
No | 324 | 77.9% | |
Yes | 92 | 22.1% | ||
Sputnik n = 380 |
No | 312 | 82.1% | |
Yes | 68 | 17.9% | ||
Sputnik light n = 92 |
No | 72 | 78.3% | |
Yes | 20 | 21.7% |
X2: chi-square test. P-value < 0.05 is considered significant
Table 3.
Hair loss | Study group (n = 2000) | |
---|---|---|
Frequency | Percent | |
1st month | 215 | 45.0% |
2nd month | 158 | 33.1% |
3rd month | 45 | 9.4% |
4th month | 36 | 7.5% |
5th month | 24 | 5.0% |
Total | 478 | 100% |
Table 4.
Vaccine type |
Study group (n = 478) |
1st month |
2nd month |
3rd month |
4th month |
5th month |
---|---|---|---|---|---|---|
AstraZeneca | n = 164 | 64 | 72 | 16 | 8 | 4 |
39.0% | 43.9% | 9.8% | 4.9% | 2.4% | ||
Johnson and Johnson | n = 4 | 0 | 4 | 0 | 0 | 0 |
0.0% | 100% | 0.0% | 0.0% | 0.0% | ||
Moderna | n = 2 | 0 | 2 | 0 | 0 | 0 |
0.0% | 100% | 0.0% | 0.0% | 0.0% | ||
Pfizer | n = 12 | 8 | 0 | 0 | 4 | 0 |
66.7% | 0.0% | 0.0% | 33.3% | 0.0% | ||
Sinopharm | n = 116 | 35 | 48 | 13 | 12 | 8 |
30.2% | 41.4% | 11.2% | 10.3% | 6.9% | ||
Sinovac | n = 92 | 32 | 32 | 8 | 8 | 12 |
34.8% | 34.8% | 8.7% | 8.7% | 13.0% | ||
Sputnik | n = 68 | 56 | 0 | 8 | 4 | 0 |
82.4% | 0.0% | 11.8% | 5.9% | 0.0% | ||
Sputnik light | n = 20 | 20 | 0 | 0 | 0 | 0 |
100% | 0.0% | 0.0% | 0.0% | 0.0% | ||
Chi-square test | X2 = 137.4, P-value < 0.001 |
X2: chi-square test. P-value < 0.05 is considered significant
Table 5.
Vaccine | Study group (n = 478) | ||||
---|---|---|---|---|---|
Acute TE | Exacerbated AGA | New onset A.A | Overlap AGA and TE | Recurrent A.A | |
Astrazeneca n = 164 |
139 (84.8%) |
1 (0.6%) |
12 (7.3%) |
8 (4.9%) |
4 (2.4%) |
Johnson and Johnson n = 4 |
4 (100%) |
0 | 0 | 0 | 0 |
Moderna n = 2 |
2 (100%) |
0 | 0 | 0 | 0 |
Pfizer n = 12 |
4 (33.3%) |
0 |
4 (33.3%) |
4 (33.3%) |
0 |
Sinopharm n = 116 |
96 (82.8%) |
4 (3.4%) |
8 (6.9%) |
0 |
8 (6.9%) |
Sinovac n = 92 |
72 (78.3%) |
4 (4.3%) |
12 (13.0%) |
0 |
4 (4.3%) |
Sputnik n = 68 |
52 (76.5%) |
4 (5.9%) |
4 (5.9%) |
4 (5.9%) |
4 (5.9%) |
Sputnik light n = 20 |
20 (100.0%) |
0 | 0 | 0 | 0 |
Total | 389 | 13 | 40 | 16 | 20 |
Chi-square test | X2 = 74.7, P-value < 0.001 |
TE telogen effluvium, AGA androgentic alopecia, A.A alopecia areata
X2: chi-square test. P-value < 0.05 is considered significant
Significant associations between TE after COVID-19 vaccination and dose number exist (p < 0.05). Three hundred forty people (17%) reported TE after the first dose, while 138 (6.9%) reported TE after the second dose. Increased risk of TE is also noted across vaccine types with similar rates (84.8, 82.8, and 33.3% for Oxford/AstraZeneca, Sinopharm, and Pfizer-BioNTech vaccines, respectively). 98.7% of participants with post-vaccination hair loss reported recovery in hair growth or cessation of hair shedding by the 6th month (Tables 4 and 5 and Figs. 1, 2, and 3).
Discussion
Telogen effluvium–associated hair loss can last up to 6 months after proper treatment as well as removal of any triggering factors. Persistence of TE for more than 6 months implies chronicity of the condition and can be more challenging to treat. In this study, we found that approximately 23.9% of patients had diffuse hair loss for 6 months (acute TE) with the majority commencing 1 month post-vaccination (45.8%) and 33.2% after the second month.
Survey participants who received one or more vaccines against COVID-19 also had a statistically significant increase in TE. Cutaneous reactions after COVID-19 vaccination have been widely reported [4]. Local injection site reactions, urticarial eruptions, and morbilliform eruptions have been reported, but delayed; large local reactions are the most common cutaneous reactions [5].
Hair lost post COVID-19 vaccination was not widely discussed in the literature; however, a study from Poland demonstrated that only 2.2% of those vaccinated complained of acute hair loss of which 46.4% and 53.6% having hair loss after the first and second doses, respectively [6]. Another study from Saudi Arabia demonstrated hair loss after COVID vaccine to be as high as 63.2% with the majority after the first dose (55.8%) and 44.2% after the second dose [7]. Another study that assessed the prevalence of TE following COVID 19 vaccination demonstrated that out of 991 participants, 670 (67.6%) reported post-vaccination hair fall. The probable causes of post-vaccination hair fall were vaccine-related in 185 (27.6%) participants, other causes in 326 (48.7%) participants, and unclear in 326 (48.7%) participants [8].
The COVID-19 pandemic has increased the levels of anxiety and stress-related disorders among individuals which contributed to hair shedding and TE. Rates of acute hair shedding during the pandemic increased for which patients requested treatments to break such cycle. Interestingly, we found that only 24.4% of patients sought medical advice, similar to the rate of 18.9% reported by Turkmen et al. [9] and 22.9% reported by Alsalhi et al. [7].
Vaccines were identified to cross react with self-antigens leading to autoimmunity and to possibly trigger reactions in genetically susceptible individuals. It is possible that the messenger RNA SARS-CoV-2 Moderna and Pfizer vaccines can trigger a T cell–mediated immune response with the downstream effects of alopecia [10].
Alopecia areata (AA), characterized by patchy hair loss from the scalp, is an autoimmune condition precipitated by loss of immune privilege in the hair bulge leading to concentrates of natural killer (NK) cells within hair follicles [11, 12]. In the present study, new onset AA and recurrent AA were among the reported hair loss features among participants.
Hair loss following SARS-CoV-2 vaccination is an increasingly reported phenomenon. Newer reports are emerging with different forms of alopecias following COVID-19 vaccination [1]. Essam et al. also reported recurrent AA after a long period of disease quiescence in a middle-aged woman following immunization with COVID-19 vaccine [13].
Induction and rapid expression of type 1 interferon (IFN) against viral vaccines to promote the release of anti-chemokines such as interleukin 12 and interleukin 23 had been implicated in the development of AA. Moreover; this exaggerated production of IFNs can contribute to suppressing immunity and further promoting the development of AA. These findings suggest a potential role of vaccines to trigger autoimmunity, as observed in patients vaccinated for hepatitis B and hepatitis A that showed a significantly higher prevalence of alopecia areata [12].
To our knowledge, the current study is considered the first study to report post-vaccination hair fall among the public in Egypt, and probably the largest with 2000 participants included. Additionally, previous reports were mainly case reports with no ability to calculate prevalence or just questionnaire-based cross-sectional studies with no trichosopic confirmation of the diagnosis. Nevertheless, a number of limitations should be acknowledged such as absence of lab investigations and relying on self-reporting of patients as well as failure of follow-up of the condition for longer durations.
Conclusion
In conclusion, we reported prevalence of post-vaccination hair fall that was confirmed by trichoscopy and which affected approximately one quarter of participants who received COVID-19 vaccines. Other factors, such as stress and infection, cannot be excluded and remain to be further investigated by larger multicenter studies.
Acknowledgements
Authors are grateful to all participants in the study.
Abbreviations
- COVID-19
Coronavirus disease (COVID-19)
- TE
Telogen effluvium
- AA
Alopecia areata
- NK cells
Natural killer cells
- IFN
Interferon
Author contribution
A.A, I.S, A.M, and M.E designed and performed the research. A.A, I.S, A.M, and M.E performed the work. A.A, I.S, A.M, and M.E analyzed and wrote the paper. All authors contributed equally in production of this work.
Funding
Open access funding provided by The Science, Technology & Innovation Funding Authority (STDF) in cooperation with The Egyptian Knowledge Bank (EKB).
Availability of data and material
The data that support the findings of this study are available from the corresponding author upon reasonable request.
Declarations
Ethics approval and consent to participate
This study protocol was reviewed and approved by ethics committee on human research by Al Azhar faculty of medicine IRB (00012367–19–07–012). All methods were performed in accordance with the relevant guidelines and regulations. Written informed consents were received from participants upon explanation of the study.
Consent for publication
Not applicable; the manuscript does not contain any individual personal data.
Competing interests
The authors have no conflicts of interest to declare.
Footnotes
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
References
- 1.Genco L, Cantelli M, Noto M, et al. Alopecia areata after COVID-19 vaccines. Skin Appendage Disord. 2023;9(2):141–143. doi: 10.1159/000528719. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Hernández Arroyo J, Izquierdo-Condoy JS, Ortiz-Prado E. A case series and literature review of telogen effluvium and alopecia universalis after the administration of a heterologous COVID-19 vaccine scheme. Vaccines (Basel) 2023;11(2):444. doi: 10.3390/vaccines11020444. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Ammar AM, Elshahid AR, Abdel-Dayem HA, et al. Dermoscopic evaluation of the efficacy of combination of topical spironolactone 5% and minoxidil 5% solutions in the treatment of androgenetic alopecia: a cross sectional-comparative study. J Cosmet Dermatol. 2022;21(11):5790–5799. doi: 10.1111/jocd.15328. [DOI] [PubMed] [Google Scholar]
- 4.Elsaie ML, Youssef EA, Nada HA. Herpes zoster might be an indicator for latent COVID 19 infection. Dermatol Ther. 2020;33(4):e13666. doi: 10.1111/dth.13666. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Elsaie ML, Nada HA. Herpes zoster (shingles) complicating the course of COVID19 infection. J Dermatolog Treat. 2022;33(2):1123–1125. doi: 10.1080/09546634.2020.1782823. [DOI] [PubMed] [Google Scholar]
- 6.Jęśkowiak I, Wiatrak B, Grosman-Dziewiszek P, et al. The incidence and severity of post-vaccination reactions after vaccination against COVID-19. Vaccines, NCBI. 2021;9(5):502. doi: 10.3390/vaccines9050502. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.AlSahli W, Almulhim Y, Issa NT. Cross-sectional study to determine the prevalence of telogen effluvium among patients experiencing COVID-19 infection or vaccination in Saudi Arabia and Arabic countries. European Journal of Molecular & Clinical Medicine. 2022;9(7):4663–4674. [Google Scholar]
- 8.Alharbi M. Telogen effluvium after COVID-19 vaccination among public in Saudi Arabia. J Family Med Prim Care. 2022;11(10):6056–6060. doi: 10.4103/jfmpc.jfmpc_377_22. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Turkmen D, Altunisik N, Sener S, Colak C. Evaluation of the effects of COVID-19 pandemic on hair diseases through a web-based questionnaire. Dermatol Ther. 2020;33(6):e13923. doi: 10.1111/dth.13923. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Tassone F, Cappilli S, Antonelli F, et al. Alopecia areata occurring after COVID-19 vaccination: a single-center, cross-sectional study. Vaccines. 2022;10(9):1467. doi: 10.3390/vaccines10091467. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Elsaie ML, Hasan MS. Successful treatment of long-standing alopecia totalis with intralesional methotrexate. J Cosmet Dermatol. 2022;21(2):855–856. doi: 10.1111/jocd.14117. [DOI] [PubMed] [Google Scholar]
- 12.Elshahid AR, Kadah AS, Hassan EA, Elsaie ML. Efficacy of Jessener solution versus intralesional steroid in treatment of alopecia areata. J Cosmet Dermatol. 2023;22(2):529–533. doi: 10.1111/jocd.15546. [DOI] [PubMed] [Google Scholar]
- 13.Essam R, Ehab R, Al-Razzaz R. Alopecia areata after ChAdOx1 nCoV-19 vaccine (Oxford/AstraZeneca): a potential triggering factor? J Cosmet Dermatol. 2021;20(12):3727–3729. doi: 10.1111/jocd.14459. [DOI] [PMC free article] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
The data that support the findings of this study are available from the corresponding author upon reasonable request.