Psoriasis
Chronic immune-mediated inflammatory skin disease affecting ~2–3% of the UK population. Characterised by well-demarcated, erythematous plaques with silvery scale, typically on extensor surfaces and scalp. Driven by Th17/IL-23 pathway. Associated with psoriatic arthritis (up to 30%), cardiovascular disease, metabolic syndrome, and depression.
Key Facts
Prevalence: ~2–3% of UK population; equal sex distribution; bimodal onset (16–22 and 55–60 years) Chronic plaque psoriasis: most common type (~90%); well-demarcated erythematous plaques with silvery scale on extensor surfaces Auspitz sign: punctate bleeding on removal of scale (exposure of dermal papillae) Koebner phenomenon: new lesions at sites of skin trauma Nail changes: pitting, onycholysis, oil drop sign, subungual hyperkeratosis (~50% of patients) Psoriatic arthritis: develops in up to 30%; screen with PEST questionnaire Th17/IL-23 axis: central to pathogenesis; targeted by biologics (secukinumab, ixekizumab, guselkumab) NICE CG153: psoriasis assessment and management; biologics via NICE TA pathway
Overview
Key Facts
Psoriasis is a systemic inflammatory disease, not just a skin condition. Cardiovascular risk is independently increased and should be actively managed. Biologic therapies have transformed outcomes for severe disease.
Epidemiology
- UK prevalence: 2–3% (~1.8 million people)
- Bimodal onset: type I (16–22 years, HLA-Cw6+, family history) and type II (55–60 years)
- 30% have first-degree relative with psoriasis
- Increased cardiovascular mortality: severe psoriasis shortens life expectancy by ~5 years
Aetiology
- Genetic: HLA-Cw6 (strongest association), multiple susceptibility loci (PSORS1-9)
- Environmental triggers: streptococcal pharyngitis (guttate), stress, drugs (lithium, beta-blockers, antimalarials, NSAIDs, ACEi withdrawal of steroids), alcohol, smoking, trauma (Koebner)
Pathophysiology
- Dendritic cell activation → IL-23 production → Th17 cell differentiation → IL-17A, IL-22 production
- Keratinocyte hyperproliferation: cell cycle reduced from 28 days to 3–4 days → accumulation of immature keratinocytes → silvery scale
- Angiogenesis: dilated tortuous capillaries in dermal papillae
- TNF-alpha also contributes: targeted by anti-TNF biologics
Clinical Presentation
Chronic Plaque Psoriasis (~90%)
- Well-demarcated, erythematous plaques with silvery-white scale
- Symmetrical; extensor surfaces (elbows, knees), scalp, sacrum, umbilicus
- Pruritus in ~70%
Guttate Psoriasis
- Small (<1cm) drop-like papules over trunk and proximal limbs
- Often triggered by streptococcal pharyngitis (2–4 weeks prior)
- Common in children/young adults; may be first presentation
Other Types
- Flexural (inverse): smooth, glazed erythema in flexures; minimal scale
- Pustular: localised (palmoplantar) or generalised (von Zumbusch — emergency)
- Erythrodermic: >90% BSA; risk of hypothermia, cardiac failure — EMERGENCY
Nail Psoriasis (~50%)
- Pitting, onycholysis, oil drop sign, subungual hyperkeratosis
Red Flags
- Generalised pustular psoriasis (systemic illness, fever)
- Erythrodermic psoriasis (hypothermia, high-output cardiac failure)
- Rapid worsening after systemic steroid withdrawal
Differential Diagnosis
| Diagnosis | Key Features | Investigation |
|---|---|---|
| Eczema | Flexural, poorly demarcated, personal/family atopy | Clinical |
| Tinea corporis | Annular, asymmetric, leading scaly edge | Skin scraping, KOH |
| Pityriasis rosea | Herald patch, Christmas tree distribution, self-limiting | Clinical |
| Lichen planus | Purple, polygonal, pruritic papules; Wickham's striae | Biopsy |
| Secondary syphilis | Palms/soles rash, condylomata lata, sexual history | Syphilis serology |
| Mycosis fungoides (CTCL) | Patches/plaques, bathing trunk distribution | Skin biopsy |
Diagnosis / Investigation
Clinical Diagnosis
- Usually clinical; no investigations needed for typical plaque psoriasis
Severity Assessment
- BSA, PASI, DLQI: required for biologic eligibility (PASI ≥10 and DLQI ≥10)
- PEST questionnaire: screen for psoriatic arthritis
Pre-Treatment Bloods (if systemic therapy)
- FBC, U&Es, LFTs: baseline before methotrexate/ciclosporin
- Hepatitis B/C, HIV: before biologics
- TB screening (IGRA): before anti-TNF biologics
- Lipid profile, HbA1c, BP: cardiovascular risk assessment
Special Tests
- Skin biopsy: if diagnostic uncertainty — regular acanthosis, Munro microabscesses, parakeratosis, dilated capillaries
- Throat swab/ASO titre: if guttate (streptococcal trigger)
- Joint imaging: if psoriatic arthritis suspected (X-ray: pencil-in-cup, periostitis)
Management
Topical (Mild-Moderate)
- Vitamin D analogues: calcipotriol (Dovonex) OD-BD; combined with betamethasone (Dovobet/Enstilar)
- Topical corticosteroids: potent (betamethasone valerate 0.1%) for body; moderate for face/flexures
- Coal tar preparations: for chronic stable plaques; messy but effective
- Dithranol: short-contact therapy in specialist settings
- Emollients: adjunctive; descale before active treatment
Phototherapy (Moderate)
- Narrowband UVB: first-line for moderate-extensive disease; 2–3× weekly for 6–8 weeks
- PUVA: psoralen + UVA — more effective but higher skin cancer risk; limited courses
Systemic (Moderate-Severe)
- Methotrexate: 7.5–25mg weekly (PO or SC) + folic acid 5mg weekly (not same day); monitor FBC, LFTs
- Ciclosporin: 2.5–5mg/kg/day; rapid onset; limit to 1–2 years (nephrotoxicity, hypertension)
- Acitretin: 25–50mg OD; retinoid; teratogenic — women must avoid pregnancy for 3 years after stopping
- Apremilast: PDE4 inhibitor; 30mg BD; oral; fewer monitoring requirements
Biologics (Severe — NICE TA)
- Anti-TNF: adalimumab 40mg alternate weeks, etanercept 50mg weekly
- Anti-IL-17: secukinumab 300mg monthly, ixekizumab, bimekizumab
- Anti-IL-23: guselkumab 100mg every 8 weeks, risankizumab
- Anti-IL-12/23: ustekinumab 45mg every 12 weeks
- Entry criteria: PASI ≥10 AND DLQI ≥10, failed standard systemic therapy
Referral Criteria
- Dermatology: moderate-severe psoriasis, diagnostic uncertainty, biologic consideration
- Rheumatology: suspected psoriatic arthritis
- Urgent: generalised pustular or erythrodermic psoriasis
Prognosis
- Chronic condition: no cure; management aims for control
- Guttate psoriasis: ~60% resolve spontaneously; ~30% develop chronic plaque psoriasis
- Biologics: PASI 90 achieved in 60–80% with modern anti-IL-17/IL-23 agents
- Cardiovascular risk: severe psoriasis independently increases CV mortality; manage risk factors actively
- Quality of life: DLQI improvement is a key treatment target
Other Relevant Information
Psoriasis Treatment Ladder
| Step | Treatment |
|---|---|
| 1 | Emollients + topical vitamin D/steroid |
| 2 | Phototherapy (NB-UVB) |
| 3 | Standard systemic (MTX, ciclosporin, acitretin) |
| 4 | Biologics (anti-TNF, anti-IL-17, anti-IL-23) |
PASI Score
| Score | Severity |
|---|---|
| <5 | Mild |
| 5–10 | Moderate |
| >10 | Severe |
| PASI 75 response | 75% improvement from baseline (treatment target) |