Alopecia Areata
Alopecia Areata
Alopecia Areata
Corresponding author:
Dr. Amer Omer Bin Al-Zou
Associate Professor, Dermatology,
Faculty of Medicine, University of Aden, Yemen.
Mobile: +967 736 361 344
Email: amer_zou2009@yahoo.com
Abstract
Objective: The aim of the study was to describe the Family history was positive among 9.9% of
demographic and clinical characteristics of alopecia patients and the most of alopecia areata patterns
areata and to determine the associated diseases were patchy with (83.3%).
among patients.
Also, multiple patches were the most common type
Materials and method: This is a retrospective study (60.0%) followed by single patches (33.3%).
of all patients who presented with alopecia areata
and who were seen in our two private dermatology Pitting was the most common presenting nail chang-
clinics in Aden. The patients’ charts retrieved ob- es, being found in (11.6%) patients. Atopic derma-
tained the study data. The data was analyzed using titis (4.4%), hypothyroid (2.8%), were the most
SPSS version 17. common comorbidities. The most site involvement
was the scalp (89.2%). The mean disease duration
The relationships between study variables and sex at the time of presentation for all patients was 3.7
were examined using Pearson’s Chi-square Test. months.
Significance was considered at P value ≤ 0.05.
Conclusion: This study highlights the importance of
Results: The total patients were 264 (females 61.7% further studies in this field.
and males 38.3%).
Key words: Alopecia areata, clinical characteristics,
The mean age of patients was 18 years. The rela- associated diseases, Aden
tion between age and means of gender were statis-
tically highly significant (p = 0.000).
WORLD FAMILY MEDICINE/MIDDLE EAST JOURNAL OF FAMILY MEDICINE VOLUME 19 ISSUE 7 JULY 2021
70 M I D D L E E A S T J O U R N A L O F FA M I LY M E D I C I N E • V O LU M E 7 , I S S U E 1 0
P O P U L AT I O N A N D CO M M U N I T Y S T U D I E S
Results
A total of 264 alopecia areata patients were included during the study period; out of them 163 (61.7%) were females
and 101 (38.3%) were males, with a female to male ratio of 1.6:1. The mean age of females was 15.8 years (SD = ±11.6
years) and the age ranged between 1 year to 58 years, while the mean age of males was 21.4 years (SD = ±12.1 years)
and the age ranged between 1 year to 60 years.
The mean age of all patients was 18 years (SD = ±12.1 years) and the age ranged from 1 year to 60 years. The relation
between means showed statistically highly significant (p = 0.000).
* SD = Standard deviation
P = 0.000
Table 2 shows the age group 1 – 10 years represented 97 (36.7%) cases, followed by the age group 11 – 20 years with
64 (24.1%) cases, the age group 21 – 30 years with 63 (23.9%), and the age group 31 – 40 years with 30 (11.4%).
The age group 41 – 50 years were 8 (3.2%) patients and the age group ≥ 51 years were 2 (0.8%). It is also, noted that
in male patients the peak age of onset was in the ages 21-30 years with 35 (13.3%).
Ninety (96%) of the cases occurred in the age of 40 years and less than 40 years.
The difference between values of gender related to age groups is statistically significant (p = 0.003), (Table 2).
Also, Table 2 reveals that in 26 (9.9%) patients, their families had a history of the disease. They were 15 (5.7%) females
and 11 (4.2%) males, (p-value > 0.05).
WORLD FAMILY MEDICINE/MIDDLE EAST JOURNAL OF FAMILY MEDICINE VOLUME 19 ISSUE 7 JULY 2021
M I D D L E E A S T J O U R N A L O F FA M I LY M E D I C I N E • V O LU M E 7 , I S S U E 1 0 71
P O P U L AT I O N A N D CO M M U N I T Y S T U D I E S
Most alopecia areata patterns were patchy with 220 (83.3%) followed by patchy + ophiasis with 27 (10.2%), alopecia
universalis 8 (3%), alopecia totalis 7 (2.7%) and alopecia ophiasis 2 (0.8%), (p-value > 0.05); see images 1 and 2.
Table 2 also illustrates the number of patches. Multiple patches were the most common type 161 (61.0%) followed by
single patches 88 (33.3%), see images 3 and 4.
Pitting was the most common presenting nail changes, being found in 30 (11.6%) patients followed by trachyonychia in
6 (2.4%) patients and were more common in male patients 5 (2.0%) cases.
We found 3 (1.2%) cases of leuconychia and 2 (0.8%) cases of Beau’s line and both nail changes were in female
patients.
The difference between values of gender related to nail changes is statistically not significant (p > 0.05), as shown in
Table 2.
Table 2: Distribution of demographic and clinical characteristics related to sex of the study patients (n=264)
WORLD FAMILY MEDICINE/MIDDLE EAST JOURNAL OF FAMILY MEDICINE VOLUME 19 ISSUE 7 JULY 2021
72 M I D D L E E A S T J O U R N A L O F FA M I LY M E D I C I N E • V O LU M E 7 , I S S U E 1 0
P O P U L AT I O N A N D CO M M U N I T Y S T U D I E S
Associated diseases were found in 27 (10.8%) patients. Atopic dermatitis 11 (4.4%), Hypothyroid 7(2.8%), were the
most common comorbidities, followed by vitiligo in 4 (1.6%) patients, hyperthyroidism and diabetes mellitus each were
found in 2 (0.8%) patients. Down syndrome was found in 1 (0.4%) patient, as shown in Table 3.
Also, Table 3 reveals the most site involvement is the scalp 237 (89.2%) followed by a few percentages of different sites:
universalis 8 (3.2%), scalp + eye brows 6 (2.4%), scalp + barbae + moustache 6 (2.4%), scalp + barbae 5 (2.0%) and
scalp + eye brows + moustache 2 (0.8%).
Table 3: Frequency of associated diseases and site involvement of patients with alopecia areata (n=264)
Table 4 shows the mean disease duration at the time of presentation for all patients was 3.7 months (for females was
3.7 and for males was 3.9 months).
* SD = Standard deviation
P > 0.05
WORLD FAMILY MEDICINE/MIDDLE EAST JOURNAL OF FAMILY MEDICINE VOLUME 19 ISSUE 7 JULY 2021
M I D D L E E A S T J O U R N A L O F FA M I LY M E D I C I N E • V O LU M E 7 , I S S U E 1 0 73
P O P U L AT I O N A N D CO M M U N I T Y S T U D I E S
Image 3: Multiple patches alopecia areata Image 4: Single patch alopecia areata
WORLD FAMILY MEDICINE/MIDDLE EAST JOURNAL OF FAMILY MEDICINE VOLUME 19 ISSUE 7 JULY 2021
74 M I D D L E E A S T J O U R N A L O F FA M I LY M E D I C I N E • V O LU M E 7 , I S S U E 1 0
P O P U L AT I O N A N D CO M M U N I T Y S T U D I E S
WORLD FAMILY MEDICINE/MIDDLE EAST JOURNAL OF FAMILY MEDICINE VOLUME 19 ISSUE 7 JULY 2021
M I D D L E E A S T J O U R N A L O F FA M I LY M E D I C I N E • V O LU M E 7 , I S S U E 1 0 75
P O P U L AT I O N A N D CO M M U N I T Y S T U D I E S
The frequency of these concurrent diseases varies dermatitis, hypothyroid, vitiligo, hyperthyroidism, diabetes
between geographically separate populations, which mellitus and Down syndrome. This study highlights the
may suggest genetic variability within these different importance of further studies in this field.
populations [34].
References
Severe alopecia areata might be accompanied by nail
changes [20].
1. Gilhar A, Etzioni A, Paus R. Alopecia Areata. New
England Journal of Medicine. 2012; 366: 1515-1525.
Atopic diseases, such as sinusitis, asthma, rhinitis, and
2. Healy E, Rogers S. PUVA treatment for alopecia areata-
especially atopic dermatitis, are also more common than
does it work? A retrospective review of 102 cases. Br J
expected in populations with alopecia areata, and are
Dermatol. 1993; 129(1):42-4.
associated with early-onset and more severe forms of hair
3. Goh C, Finkel M, Christos PJ, Sinha AA. Profile
loss [33].
of 513 patients with alopecia areata: associations of
disease subtypes with atopy, autoimmune disease and
In a Korean population, atopic dermatitis was significantly
positive family history. J Eur Acad Dermatol Venereol.
more common in patients with early-onset alopecia areata,
2006;20:1055-1060
whereas thyroid disease (hyperthyroidism, hypothyroidism,
4. Tosti A, Whiting D, Iorizzo M, et al. The role of scalp
goiter and thyroiditis) was the most common in late-onset
dermoscopy in the diagnosis of alopecia areata incognita.
disease [35]; similar findings were reported by Ranawaka
J Am Acad Dermatol.
[31] from Sri Lanka.
2008;59:64-67
5. Alkhalifah A, Alsantali A, Wang E, McElwee KJ,
In a review of 17 studies, investigators found higher
Shapiro J. Alopecia areata update: part I. Clinical picture,
odds of atopic dermatitis in patients with alopecia totalis
histopathology, and pathogenesis. J Am Acad Dermatol
or alopecia universalis compared to those with patchy
2010;62:177-188
alopecia areata [36].
6. McMichael AJ. The genetic epidemiol autoimmune
pathogenesis alopecia areata. J Eur. Acad. Dermatol.
In our study, we found the most site involvement is the
Venereol. 1997; 9:36-43.
scalp 237 (89.2%). Alsaiari et al [29] reported that the
7. McDonagh AJ, Tazi-Ahnini R. Epidemiology and
scalp was found to be the most commonly affected site
genetics of alopecia areata. Clin. Exp. Dermatol. 2002;
(82.4%).
27:405-409.
8. Tosti A, Bellavista S, Iorizzo M. Alopecia areata: A long
Previous studies reported that the scalp is the most
term follow-up study of 191 patients. J Am Acad Dermatol.
common site of involvement, with or without involvement
2006; 55: 438-41.
of other body sites (such as the eyebrows, eyelashes, and
9. Amin SS, Sachdeva S. Alopecia areata: a review. J
beard) [21,25].
Dermatol Dermatol Sur. 2013; 17: 37–45.
10. Mounsey AL, Reed SW. Diagnosing and treating hair
Alopecia totalis and universalis occurred in 7.3% of AA
loss. Am Fam Physician. 2009;80:356–362.
cases and always occurred before the age of 30 years
11. Miteva M, Villasante A. Epidemiology and burden of
[21].
alopecia areata: a systematic review, Clinical, Cosmetic
and Investigational Dermatology. 2015; 8: 397–403.
In our study, we found the mean disease duration at the
12. Lundin M, Chawa S, Sachdev A, et al. Gender
time of presentation for all patients was 3.7 months (for
differences in alopecia areata. Journal of Drugs in
females was 3.7 and for males was 3.9 months).
Dermatolology. 2014; 13(1): 409–413.
Alsaiari et al [29] reported in their study from Najran in
13. Kavak A, Yeşildal N, Parlak AH, Gökdemir G, Aydoğan
Saudi Arabia that the duration of the disease was found
I, Anul H, et al. Alopecia areata in Turkey: demographic
to be extremely variable and the majority of the patients
and clinical features. J Eur Acad Dermatol Venereol.
(67.6%) suffered from alopecia for more than 1 year.
2008; 22(8):977–981.
14. Ranawaka RR. An observational study of alopecia
Conclusion areata in Sri Lankan adult patients. Ceylon Med J. 2014;
59:128–131. [PubMe
AA is a form of alopecia caused by autoimmune attack 15. Sharma VK, Dawn G, Kumar B. Profile of alopecia
of the hair follicles and sometimes the nail. We observed areata in Northern India. Int J Dermatol. 1996;35(1):22–
female predominance for AA and the mean age of onset of 27
AA was 18 years and the most cases occurring in the age 16. Yang S, Yang J, Liu JB, et al. The genetic epidemiology
≤ 40 years. In male patients, the peak age of onset was of alopecia areata in China. Br J Dermatol. 2004;151(1):16–
in the ages 21-30 years with 35 (13.3%). Family history 23.
of alopecia areata was positive among 9.9% of patients 17. Alshahrani AA, Al-Tuwaijri R, Abuoliat ZA, Alyabsi M,
and most AA patterns were patchy with multiple patches. AlJasser MI, et al. Dermatology Research and Practice.
Nail changes, were found in (11.6%) patients and most 2020; 4 pages. Available at: https://doi.org/10.1155/2020
site involvement was the scalp (89.2%). Several comorbid /7194270
diseases were found among our patients including atopic
WORLD FAMILY MEDICINE/MIDDLE EAST JOURNAL OF FAMILY MEDICINE VOLUME 19 ISSUE 7 JULY 2021
76 M I D D L E E A S T J O U R N A L O F FA M I LY M E D I C I N E • V O LU M E 7 , I S S U E 1 0
P O P U L AT I O N A N D CO M M U N I T Y S T U D I E S
WORLD FAMILY MEDICINE/MIDDLE EAST JOURNAL OF FAMILY MEDICINE VOLUME 19 ISSUE 7 JULY 2021
M I D D L E E A S T J O U R N A L O F FA M I LY M E D I C I N E • V O LU M E 7 , I S S U E 1 0 77