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Condition

Alopecia areata

An autoimmune condition where the immune system attacks growing hair follicles, causing round patches or total hair loss; three oral JAK inhibitors are approved for severe cases but hair usually goes again when treatment stops.

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Key takeaways

  • Follicles are attacked, not destroyed. Alopecia areata (AA) is non-scarring, so regrowth is possible, including spontaneous regrowth in milder disease. It is different from androgenetic alopecia and telogen effluvium and can coexist with them.
  • It is common and more often diagnosed in women. In a US claims study prevalence rose from 0.199% (2016) to 0.222% (2019), and roughly 5 to 10% of cases were total scalp or body hair loss (Mostaghimi 2023).
  • It travels with other autoimmune and mood conditions. A meta-analysis of 102 studies found raised odds of vitamin D deficiency, lupus (OR 5.5), vitiligo (OR 5.3), metabolic syndrome (OR 5.0) and Hashimoto thyroiditis (OR 4.3) (Ly 2023). A US cohort found more psychiatric (30.9% vs 26.8%) and autoimmune (16.1% vs 8.9%) conditions at diagnosis (Mostaghimi 2024). Thyroid disease is about 3.7 times more frequent in AA (Xin 2020); see thyroid and hair.
  • Oral JAK inhibitors are the first drugs proven to reverse severe AA. A 2026 meta-analysis of 12 trials (4,141 people) found the odds of reaching a scalp-hair score of SALT 10 or less at week 24 were 5.7 times higher than placebo, with no significant excess of serious adverse events (OR 1.04) but more adverse events overall (OR 1.60) (Morriss 2026).
  • Cochrane rates baricitinib alone as high-certainty. Among all AA treatments tested in 63 randomized studies (4,817 people), only baricitinib had high-certainty evidence of benefit (RR 7.54 for 75% or more regrowth in the short term). Most older treatments, including steroids, immunotherapy, minoxidil and cyclosporine, rest on very-low to low-certainty evidence (Mateos-Haro 2023).
  • They are for severe disease only, are prescription-only, and carry boxed warnings in the US covering serious infections, cancer, major cardiovascular events and blood clots.
  • Stopping usually means relapse. These drugs suppress AA; they do not cure it.
  • JAK inhibitors have no proven role in pattern hair loss (see JAK inhibitors and hair).

How it works

Growing follicles normally escape immune surveillance. In AA this breaks down, autoreactive T cells attack the bulb, and signalling through JAK enzymes sustains the attack. JAK inhibitors interrupt that signalling. Patchy AA shows as one or several round smooth patches; ophiasis is a band at the nape and sides; alopecia totalis is the whole scalp and alopecia universalis all body hair. Brows, lashes and nails can be involved. Severity is scored with SALT (0 = none, 100 = complete scalp loss); severe in trials means SALT 50 or more.

What the studies show

Drug Dose in trial Trial Key result
Baricitinib 2 or 4 mg once daily BRAVE-AA1/2, 1,200 adults with SALT 50+ SALT 20 or less at week 36: 38.8% and 35.9% (4 mg) vs 6.2% and 3.3% placebo (King 2022)
Ritlecitinib 50 mg once daily ALLEGRO 2b/3, 718 aged 12+, 24 weeks SALT 20 or less: 23% vs 2% placebo (King 2023)
Deuruxolitinib 8 or 12 mg twice daily THRIVE-AA1, adults, 24 weeks SALT 20 or less: 29.6% (8 mg) and 41.5% (12 mg) vs 0.8% placebo (King 2024)
Deuruxolitinib 8 or 12 mg twice daily THRIVE-AA2, 517 adults, 24 weeks 33.0% and 38.3% vs 0.8% placebo (Tsianakas 2026)

The US approved deuruxolitinib at 8 mg twice daily. In the ritlecitinib extension, 65.1% of observed patients had SALT 20 or less at 3 years (47.1% by the more cautious last-observation method) (Senna 2026). All pivotal trials were industry-funded and there are no head-to-head comparisons, so cross-trial comparisons are unreliable. Approval status differs by region (baricitinib and ritlecitinib are approved in the US, EU and UK; deuruxolitinib in the US and, from 2026, the UK; NHS access varies) and all three are prescription-only.

Other treatments:

  • Topical or injected corticosteroids are the usual first step for limited patches. The German guideline gives topical corticosteroids its main topical recommendation and offers JAK inhibitors to adults, with other options for children and teens (Blume-Peytavi 2026).
  • Topical minoxidil had RR 2.31 versus placebo in two small studies, with very-low-certainty evidence (Mateos-Haro 2023).
  • Microneedling and PRP have small, low-quality AA data. Camouflage options include wigs, brow tattooing and scalp micropigmentation, and counselling helps.

Side effects and safety

Oral JAK inhibitors are linked to serious infections, shingles, blood clots, cardiovascular events, cancer and lab changes in lipids and creatine kinase (Morriss 2026). Common effects include headache and acne. Screening, vaccination and monitoring belong to the prescriber, and pregnancy is a concern with JAK inhibitors generally.

Hair type notes

  • Any hair type can be affected; patches are easiest to spot in short or straight hair, and tight styles over a patch can add traction injury (traction alopecia).
  • AA scalps are usually normal-looking and not scaly. Flaking or scarring points to other diagnoses such as tinea capitis or lichen planopilaris.
  • Only some JAK inhibitors are licensed for ages 12 and up.
  • No good evidence shows that stress alone, diet or supplements cause or cure AA.

Bottom line

See a doctor for any sudden patch, scarring, pain or rapid loss; blood tests for thyroid and vitamin D are commonly done. Mild patchy AA often regrows, and corticosteroids are the usual first step. For severe or long-lasting loss, a dermatologist can discuss JAK inhibitors, their monitoring, cost and the relapse risk. Support for mood matters too. Discuss with a doctor.

Studies 12

Mostaghimi A et al. Trends in prevalence and incidence of alopecia areata, alopecia totalis, and alopecia universalis among adults and children in a US employer-sponsored insured population. JAMA Dermatol. 2023

Design
cohort
Who
US employer-insured adults and children

Tested: claims-data analysis

Result: Prevalence rose from 0.199% (2016) to 0.222% (2019); about 5-10% had totalis or universalis; higher in women and adults.

Read the study ↗

Ly S et al. Comorbid conditions associated with alopecia areata: systematic review and meta-analysis. Am J Clin Dermatol. 2023

Design
meta analysis
People
680,823
Who
people with alopecia areata (102 studies)

Tested: comorbidity analysis

Result: Raised odds of vitamin D deficiency, lupus (OR 5.5), vitiligo (OR 5.3), metabolic syndrome (OR 5.0) and Hashimoto thyroiditis (OR 4.3).

Read the study ↗

Mostaghimi A et al. Immune-mediated and psychiatric comorbidities among patients newly diagnosed with alopecia areata. JAMA Dermatol. 2024

Design
cohort
Who
US patients newly diagnosed with alopecia areata

Tested: comorbidity comparison with controls

Result: More psychiatric (30.9% vs 26.8%) and autoimmune (16.1% vs 8.9%) conditions at diagnosis, and higher risk of new ones afterward.

Read the study ↗

Xin. Increased incidence of thyroid disease in alopecia areata: SR and MA. 2020

Design
meta analysis
People
7,517
Who
2,850 alopecia areata cases and 4,667 controls (17 studies)

Result: Thyroid disease more prevalent in alopecia areata (OR 3.66).

Read the study ↗

Morriss S et al. Efficacy and safety of oral Janus kinase inhibitors in adults and adolescents with alopecia areata: systematic review and meta-analysis of RCTs. Am J Clin Dermatol. 2026

Design
meta analysis
People
4,141
Duration
24 weeks
Who
adults and adolescents with alopecia areata (12 RCTs)

Tested: oral JAK inhibitors vs placebo

Result: Odds of SALT 10 or less were 5.7 times higher than placebo; serious adverse events not significantly raised (OR 1.04), all adverse events more common (OR 1.60).

Read the study ↗

Mateos-Haro M et al. Treatments for alopecia areata: a network meta-analysis. Cochrane Database Syst Rev. 2023

Design
systematic review
People
4,817
Who
people with alopecia areata (63 RCTs)

Tested: all studied treatments

Result: Baricitinib was the only treatment with high-certainty evidence of benefit; for oral prednisolone or cyclosporine versus placebo the evidence was very uncertain.

Read the study ↗
Show 6 more studies

King B et al. Two phase 3 trials of baricitinib for alopecia areata. N Engl J Med. 2022

Design
rct
People
1,200
Duration
36 weeks
Who
adults with severe alopecia areata (654 and 546 in two trials)

Tested: baricitinib 2 mg or 4 mg daily vs placebo

Result: At least 80% scalp hair at week 36: 38.8% (4 mg), 22.8% (2 mg), 6.2% (placebo) in trial 1; 35.9%, 19.4%, 3.3% in trial 2.

Read the study ↗

King B et al. Efficacy and safety of ritlecitinib in adults and adolescents with alopecia areata: a randomised, double-blind, multicentre, phase 2b-3 trial. Lancet. 2023

Design
rct
People
718
Duration
24 weeks
Who
people aged 12 and older with at least 50% scalp hair loss

Tested: ritlecitinib 10, 30 or 50 mg daily, with or without a 200 mg loading dose, vs placebo

Result: At least 80% scalp hair at week 24 in 23% on 50 mg vs 2% on placebo, and 31% with the loading dose; Pfizer-funded.

Read the study ↗

King B et al. Efficacy and safety of deuruxolitinib in adults with severe alopecia areata: THRIVE-AA1 phase 3 randomized, controlled trial. J Am Acad Dermatol. 2024

Design
rct
Duration
24 weeks
Who
adults aged 18 to 65 with at least 50% hair loss

Tested: deuruxolitinib 8 mg or 12 mg twice daily vs placebo

Result: At least 80% scalp hair in 29.6% (8 mg), 41.5% (12 mg) and 0.8% (placebo); Sun-funded.

Read the study ↗

Tsianakas A et al. Deuruxolitinib in severe alopecia areata: THRIVE-AA2 phase 3 trial. J Am Acad Dermatol. 2026

Design
rct
People
517
Duration
24 weeks
Who
adults with severe alopecia areata

Tested: deuruxolitinib 8 mg or 12 mg twice daily vs placebo

Result: At least 80% scalp hair at week 24 in 33.0% (8 mg), 38.3% (12 mg) and 0.8% (placebo).

Read the study ↗

Senna M et al. Long-term efficacy and safety of ritlecitinib in alopecia areata: 3-year results. Am J Clin Dermatol. 2026

Design
cohort
People
191
Duration
3 years
Who
people with alopecia areata in an open-label extension

Tested: ritlecitinib 50 mg daily

Result: At least 80% scalp hair at 3 years in 65.1% observed (47.1% with missing data carried forward); 88 to 90% of year-1 responders kept it.

Read the study ↗

Blume-Peytavi U et al. S3 guideline diagnostics and therapy in alopecia areata, part 2. J Dtsch Dermatol Ges. 2026

Design
guideline
Who
people with alopecia areata

Tested: treatment recommendations

Result: Topical corticosteroids have the main topical recommendation; JAK inhibitors are recommended for adults, with other options for children and teens.

Read the study ↗