Alopecia areata (overview) L63.8

Author: Prof. Dr. med. Peter Altmeyer

Co-Autor: Dr. med. Antje Polensky

All authors of this article

Last updated on: 05.02.2024

Dieser Artikel auf Deutsch

Synonym(s)

alopecia areata; Area Celsi; Circular hair loss; Hair Loss; Pélade

History
This section has been translated automatically.

Celsus, 30-60 AD; Sauvages, 1706

Definition
This section has been translated automatically.

Mostly reversible, sudden onset, asymptomatic, circular hair loss of varying severity and unknown cause (autoimmunological factors are discussed), histomorphologically based on anagen effluvium. Rare are foudroyant courses with complete baldness ("balding overnight").

The severity of alopecia areata can be classified with the SALT score. This is calculated from the extent and degree of hair loss on the scalp and can also be used to monitor therapy.

Classification
This section has been translated automatically.

A distinction is made between:

Occurrence/Epidemiology
This section has been translated automatically.

Incidence unclear; concerns about 1% of the dermatological patients. The lifetime risk for the occurrence of alopecia areata is 1.7%. The prevalence is given as 0.1-0.2%. There is no clear sex preference.

Etiopathogenesis
This section has been translated automatically.

Discussed are:

  • Infectious allergic triggering!
  • Genetic predisposition (e.g. gene locus TRAF1/C5); in trisomy 21/(Down syndrome, alopecia areata occurs with an above-average frequency of 10% of cases.
  • Autoimmunological factors (frequent comorbidity with thyroid diseases, around 20% of patients show an increase in anti-TPO antibodies or anti-TG antibodies)
  • AA and celiac disease: A correlation between AA and celiac disease (CD) was first shown in 1995 (Corazza GR et al. 1995) and confirmed in subsequent studies, with prevalence estimates ranging from 1:85 to 1:116 (Mascart-Lemone F et al. 1995; Hallaji Z et al. 2011). A higher prevalence of alopecia areata and Vitiliga was found in patients with dermatitis herpetiformis compared to the general population. An increased prevalence of anti-gliadin antibodies is also associated with severe AA (alopecia universalis) (Mokhtari F et al. 2016). Ertekin et al. found that 41.7% of pediatric AA patients tested positive for IgA anti-tG antibodies. These patients showed total villous atrophy (Marsh type-IIIc) on intestinal biopsy (Ertekin V et al. 2014). Hair growth was restored when gluten was eliminated. These findings imply CD screening for pediatric AA patients. Note: However, a later study (2016) found no significant difference in serologic CD markers between case and control groups (p=0.35), indicating the need for alternative CD detection methods (Mokhtari F et al. 2016). SUMMARY: Despite limited evidence, a GFD trial is recommended for refractory AA cases (Muddasani S et al. 2021/Rusk AM et al. 2021).
  • AA and vitamin D: AA patients often have lower serum vitamin D levels than control groups. The prevalence of vitamin D deficiency is also higher. The authors therefore recommend checking vitamin D levels in patients with circular hair loss.

  • AA and atopic diathesis (familial occurrence in 10-25% of cases, frequent concordant occurrence in monozygotic twins and associations with various HLA markers: DR-4, DR-5, DR-6, DR-7, DR-11, DQ3, DQB-1)
  • AA and psychological factors (possible; scientific evidence lacking)
  • AA and environmental factors (e.g. toxins) are discussed, sustainable evidence is lacking

Immunology: Affected hair follicles lose their "immune privilege" (hair follicles are protected from attacks by the immune system due to a lack of MHC and ICAM-1 expression) and, in contrast to healthy hair follicles, express more surface molecules of the MHC and ICAM class. This enables the presentation of hair follicle antigens. The detection of these autoantigens and the detection of CD4 and CD8 lymphocytes suggests a T-cell-mediated autoimmune pathogenesis. However, CD8 T cells appear to play a central role in the pathogenesis: depletion of CD8 cells leads to hair growth. The Janus kinase (JAK) signaling pathway appears to play an important role in this process. JAK inhibitors (ruxolitinib) have been used successfully in some patients. Further molecular biological findings such as increased expression of cytokines (IL-1 beta, IL-2 and interferon gamma) in lesional scalp still need to be evaluated. The initiators of this process are unknown.

Manifestation
This section has been translated automatically.

Frequency peaks in the 2nd and 3rd decade of life. According to statistics, only about 6% of patients are older than 60 years. The youngest patient described was 2 months old.

No clear sex preference, although female predominance is noted in some collectives (m:w=3:7).

Familial clustering detectable (about 25-30% of patients; association with trisomy 21 and variations in the TRAF1 gene - Redler S et al. 2010).

Localization
This section has been translated automatically.

In most cases the capillitium is affected (about 70%).

Other sites are:

  • eyebrows and eyelashes (1,5%)
  • Whiskers (1.5%)
  • underarm and pubescent hair
  • Rarely extremities or trunk hairs.

Clinical features
This section has been translated automatically.

Clinical course:

  • The clinical picture can be extraordinarily variable. The disease usually begins with a single focus of complete health, so to speak "overnight". Local symptoms are absent.
  • Typically, there are circular, centrifugally spreading, possibly confluent, non-inflammatory, rather pale bald patches (no erythema formation in the affected areas).
  • In the active marginal area, tufts of hair can be painlessly pulled out as telogenic or dystrophic hairs (see hair cycle below).
  • In the active marginal area, pathological stubby hairs are produced (exclamation mark hairs, cadaver hairs - see fig. below).
  • Follicles always remain visibly intact (important differentiation from scarring alopecias, in which the follicles are destroyed).
  • After weeks to months, hair growth starts again; frequently, regrowing hairs are depigmented. The temporal course of a.a. is mostly chronic, accompanied by relapses and remissions. Relapses can lead to extensive infestation or even universal baldness within a few days.
  • A striking observation is that in mottled gray patients, the gray hairs are initially spared. In the case of massive hair loss, this can lead to "greying overnight".

There are 4 degrees of severity:

  • Grade 1: Single foci or multiple foci, < 30% of the capillitium.
  • Grade 2: Multiple foci > 30% of the capillitium
  • Grade 3: Alopecia of the entire capillitium (alopecia areata totalis)
  • Grade 4: Alopecia of the entire integument (alopecia areata universalis).

Prognostically unfavourable sign with regard to the progression of the foci: exclamation mark hairs or comma hairs as well as cadaveric hairs in the form of comedone-like "points noirs".

Histology
This section has been translated automatically.

Dense, lymphocytic perifollicular infiltrate with focal follicular infiltration: Only hair follicles of the anagen phase are affected. Pathology: Damage of the follicle by the infiltrate; interruption of the anagen phase; dystrophy of the hair shaft with resulting breakage, incomplete keratinization (exclamation mark hair) or loss. Reduction to a miniature follicle; cyclic renewal of the hair follicle (catagen/telogen) is maintained, while the infiltrate recedes. The new anagen phase leads either to a new infiltrate attack or spontaneous hair growth.

Differential diagnosis
This section has been translated automatically.

Therapy
This section has been translated automatically.

Therapy trials should have proven their effectiveness in controlled studies. They should continue to achieve a cosmetically satisfactory result and have no serious or lasting side effects.

General therapy
This section has been translated automatically.

In mild forms, the external therapy options can be exhausted; in rapidly progressive forms, internal therapy can be used directly.

Resistance to therapy: In case of alopecia that cannot be influenced therapeutically, a wig should be prescribed. In extensive cases of alopecia areata this should of course be done at the start of therapy.

External therapy
This section has been translated automatically.

Glucocorticoids, topical: Brush single foci 2 times/day, e.g. prednicarbate (Dermatop solution), mometasone furoate (e.g. Ecural solution), triamcinolone acetonide (e.g. Volon A tincture). Treat up to about 1 cm into the healthy-appearing area. Therapy results are unsatisfactory.

Alternative: Intrafocal, strictly intracutaneous injections (use of a dermojet) of triamcinolone crystal suspension (e.g. Volon A 10 diluted 1:3 with LA such as mepivacaine), are therapy of choice for treatment of single foci. Caveat. Injections in the temporal and anterior parietal region, risk of crystals spreading into the retinal arteries with subsequent blindness. Hair regrowth approx. 4-6 weeks after start of treatment. Long-term success is questionable.

Alternative: Calcineurin inhibitors: In studies Pimecrolimus (e.g. Elidel) was applied 2 times/day to the lesional areas. Good results are explicitly described in alopecia areata in the context of the atopic group of forms. Currently, calcineurin antagonists are only approved for the treatment of atopic eczema, so that their use in alopecia areata is off-label. Strictest indication because of unclear long-term side effects!

Alternative: Dithranol: Also described is the production of toxic contact ec zema by dithranol, initially 0.05%, in increasing concentration. Daily applications. Education about dithranol therapy required (see also under psoriasis vulgaris).

Alternative: benzyl nicotinate: hyperemization with 2% benzyl nicotinate or other substances stimulating blood circulation (e.g. head tincture hyperemizing, Rubriment). Application of the essences on the hairless areas. After introduction, the patient can perform this treatment independently, if necessary.

Imiquimod (Aldara 5% cream): Casuistry reports good results (off-label use).

Other:

  • External treatments with minoxidil (e.g., Regaine), tretinoin (e.g., Cordes VAS cream, Pigmanorm cream), or ciclosporin A may be tried.
  • Barrón-Hernández YL et al. 2017 reported good results for alopecia areata in the eyebrow and eyelid areas using the locally applicable prostaglandin derivative bimatoprost, which has a primary ophthalmologic indication (elevated intraocular pressure). A known "side effect" of this preparation is eyelash growth and increased eyelash pigmentation (see below eyelash lengthening by prostaglandin analogues).
  • Thymuskin is reported to have shown a beneficial effect on hair growth in small study cohorts.

Radiation therapy
This section has been translated automatically.

PUVA therapy locally ( PUVA bath therapy or PUVA cream therapy). Application of methoxaline is also possible in form of a PUVA-turban. Determination of the MPD to determine the initial UVA dose then slow increase of the UVA dose. Informing the patient about increased light sensitivity in the treated areas.

Recommendation: PUVA therapy 3-4 times/week. If resistance to therapy can be proven after 20-30 treatments: discontinue therapy. Proof of effectiveness from placebo-controlled studies is missing. According to our own experience, successes are verifiable, but unfortunately there is a high recurrence rate and no long-term success!

Internal therapy
This section has been translated automatically.

Glucocorticoids, systemic (numerous publications): In rapidly progressive forms, trial with methylprednisolone (e.g. Urbason), initially 20-60 mg p.o., after 2-3 weeks reduction below the Cushing's threshold. Duration of therapy: 6-8 weeks. Only morbostatic effect is to be expected, the regrown hair falls out again after discontinuation of therapy, hair is only retained in 20% of cases.

Alternative: Glucocorticoid pulse therapy: In a randomized placebo-controlled study, significant improvements were demonstrated with glucocorticoid pulse therapy (prednisolone 200 mg p.o. once a week for 3 months). An alternative pulse therapy was indicated with 5mg/kgKG p.o. every 4 weeks (repeat 9-12 times).

Alternative: Dapsone (e.g. Dapsone-Fatol): 100 mg/day p.o. for months is also said to have a favorable effect on the course of the disease in adults. The effect is controversial.

Alternative: Ciclosporin A (e.g. Sandimmun, Optoral): High doses (4-6mg/kgKG/day) may be effective in combination with glucocorticoids (prednisolone 4-5mg/p.o. /day); due to the known side effects of Ciclosporin A, treatment is only justifiable in individual cases. High recurrence rate after discontinuation of therapy.

Alternative: Ciclosporin A - low dose application: Low dose application (50-100 mg p.o./day) is currently undergoing clinical trials (with good success - personal experience).

Alternative: Methotrexate: 10-15mg p.o./week if necessary in combination with glucocorticoids (prednisolone 10-20mg p.o./day).

Alternative: In severe alopecia areata, the oral, selective Janus kinase inhibitor baricitinib (Olumiant®) can be used in accordance with the EMA. This has been approved for severe alopecia areata since 01.08.2022 (FDA and EMA). Opportunistic infections must be considered as side effects.

A JAK inhibitor has been approved on the market in Germany since November 2023. The European Commission has approved ritlecitinib (Litfulo®) for the treatment of severe alopecia areata in adults and adolescents aged 12 years and older. Ritlecitinib selectively inhibits Janus kinase 3 (JAK3) and tyrosine kinase. However, German health insurance companies do not cover the costs of this approved preparation: § 34 SGB V excludes the assumption of costs for drugs to improve hair growth.

The JAK inhibitors ruxolitinib (which has been successfully used in some patients) and tofacitinib (used at a dosage of 2x10mg/day/Jabbari et al. 2018; this therapy resulted in >50% regrowth in around 66% of patients) are classified as experimental. Both JAK inhibitors cause significant side effects with prolonged administration. They are not approved for this indication in the EU.

Supportive: Zinc hydrogenaspartate (e.g. Unizink 100®) 2 times/day 50 mg p.o. or zinc sulphate (e.g. Solvezink®) 2 times/day 200 mg p.o. for at least 6-8 weeks. In addition, biotin (vitamin H), e.g. Bio-H-Tin® 1 tbl. p.o. once a day for at least 6-8 weeks, improves hair and nail quality and reduces effluvium. These therapeutic approaches are controversially discussed.

Progression/forecast
This section has been translated automatically.

  • The prognosis depends on the extent, the number of bald patches, the duration (long clinical course means poor prognosis with regard to healing) as well as on the clinical types (the ophiasis type has a particularly poor prognosis for healing). Other prognostic factors are: first manifestation in childhood before puberty, familial occurrence, associated autoimmune diseases, existence of atopic dermatitis, nail involvement and alopecia areata totalis/ universalis.
  • As a rule of thumb, within the first 6 months, 30% of alopecia areata patients show regrowth or complete healing. Within one year it is 50%, after 5 years 75%.
  • Spontaneous regrowth usually occurs in the center of the bald spot and spreads to the periphery. Often thin, completely white downy hairs appear first, which are gradually replaced by longer often still unpigmented hairs. Only later does the hair begin to color normally. In older patients, the lesional hairs may remain white for a long time.

Tables
This section has been translated automatically.

Possible forms of treatment of alopecia areata depending on the degree of the disease

Therapy

disease severity

External

Hyperemic substances

Grade 1

vitamin A acid

Grade 1

Glucocorticoid tinctures or solutions

Grade 1

Diphenylcyclopropenone

grades 1-2

Dithranol

grades 1-3

PUVA local

grades 1-3

UV irradiation (SUP)

grades 1-4

Internal

Zinc

grades 1-4

Biotin (vitamin H)

grades 1-4

PUVA systemic

grades 2-4

Glucocorticoids

grades 3-4

Dapsone

grades 2-4

Note(s)
This section has been translated automatically.

The immunotherapy with diphenylcyclopropenone (alternatively: dibutyl squarate), formerly listed as standard therapy for alopecia areata, is obsolete today because of its side effects. It is only listed here for historical reasons:

Diphenylcyclopropenone (DPCP): Immunotherapy with contact allergens for severe, refractory forms of alopecia areata. Currently the most effective treatment modality. Caution. There are no commercial preparations (no drug in the sense of the law), the treating physician bears the full responsibility for the therapy and its NW! Single half-sided application of a 2% DPCP solution to the head to produce contact sensitization: 2-7 days of (desirable) burning and itching, eczema reaction. Next application of a highly diluted DPCP solution (0.001%) 14 days after sensitization, then 1 time/week. Slow increase of concentration. Titration to a dosage (individually very different) that causes an inflammatory reaction with redness and itching the next day and heals with scaling. Treatment 1 time/week initially for 6-12 months, possibly for years. Onset of action after approx. 10 applications. Accompanying therapy with steroid-free creams (e.g. Dermatop base cream etc.). Textile sun protection! In a larger study (142 patients) a "complete response" was observed in about 40% of the cases, a "partial response" in 15%, a "minimal response" in 20% and "no response" in about 30%.

Alternative: Square acid dibutyl ester (SADBE): Alternative to treatment with DPCP, see above.

Literature
This section has been translated automatically.

  1. Barrón-Hernández YL et al. (2017) Bimatoprost for the treatment of eyelash, eyebrow and scalp alopecia. Expert Opin Investig Drugs 26:515-522.
  2. Camacho FM et al. (1999) Zinc aspartate, biotin, and clobetasol propionate in the treatment of alopecia areata in childhood. Pediatr Dermatol 16: 336-338
  3. Celsus AC (50-60 AD) De medicina. Liber VI, Caput IV, De areis
  4. Corazza GR et al. (1995) Celiac disease and alopecia areata: report of a new association. Gastroenterology 109:1333-1337.
  5. Ertekin V et al. (2014) Screening of celiac disease in children with alopecia areata. Indian J Dermatol 59:317.
  6. Hallaji Z et al. (2011) Prevalence of anti-gliadin antibody in patients with alopecia areata: a case-control study. Tehran-Univ-Med-J 68:738-742.
  7. Haneke E (2013) Diseases of the nails. Dermatology 64: 519-532
  8. Harrison S et al. (2003) Optimal management of hair loss (alopecia) in children. Am J Clin Dermatol 4: 757-770
  9. Jabbari A et al. (2018) An Open-Label Pilot Study to Evaluate the Efficacy of Tofacitinib in Moderate toSevere Patch-Type Alopecia Areata, Totalis, and Universalis. J Invest Dermatol doi:10.1016/j.jid.2018.01.032.
  10. King B et al. (2023) Integrated safety analysis of baricitinib in adults with severe alopecia areata from two randomized clinical trials. Br J Dermatol 188:218-227
  11. Kolde G et al. (2007) Successful treatment of alopecia areata with efalizumab. JDDG 9: 834
  12. Lutz G (2015) Thyroid diseases in alopecia areata - a critical review. JDDG 13 (Suppl 1) 18
  13. Mascart-Lemone F et al. (1995) Serology of coeliac disease: early diagnosis and therapeutic impact. Acta Gastroenterol Belg 58:388-96.
  14. Mokhtari F et al. (2016) The frequency distribution of celiac autoantibodies in alopecia areata. Int J Prev Med 7:109.
  15. Muddasani S et al. (2012) Screening of celiac disease in children with alopecia areata. Indian J Dermatol 59:317.
  16. Ohlmeier MC et al. (2012) Topical immunotherapy with diphenylcyclopropenone of patients with alopecia areata - a large retrospective study on 142 patients with a self-controlled design. JEADV 26: 503-507
  17. Rusk AM et al. (2021) Gluten and skin disease beyond dermatitis herpetiformis: a review. Int J Dermatol 60:281-288.
  18. Safavi KH et al. (1989) Incidence of alopecia areata in Olmsted County, Minnessota, 1975 through 1989. Mayo Clin Proc 70: 628-633
  19. Wiseman MC et al. (2001) Predictive model for immunotherapy of alopecia areata with diphencyprone. Arch Dermatol 137: 1063-1068
  20. Xing L et al. (2014) Alopecia areata is driven by cytotoxic T lymphocytes and is reversed by JAK inhibition. Nat Med 20:1043-1049
  21. https://www.ema.europa.eu/en/medicines/human/EPAR/olumiant
  22. https://www.ema.europa.eu/en/medicines/human/EPAR/litfulo
  23. https://www.mdedge.com/dermatology/article/265433/hair-nails/european-commission-grants-approval-ritlecitinib-severe

Disclaimer

Please ask your physician for a reliable diagnosis. This website is only meant as a reference.

Authors

Last updated on: 05.02.2024