• Psoriasis = Chronic inflammatory skin disease • Characterized by red, well-demarcated plaques with silver scale • Variable severity: mild to severe forms • Prevalence : ~2% in the UK; peak onset 16–22 (early onset) & 55–60 (late onset) INTRODUCTION PSORIASIS
Epidemiology Psychological Comorbidities 01 02 03 depression, anxiety, impaired body image - psoriatic arthritis, metabolic syndrome, increased CV risk - Chronic, stigmatizing disease → affects quality of life, employment, relationships Epidemiology and Impact PSORIASIS ~2% of the UK population
Aetiology & Pathophysiology 02
Genetics • Polygenic inheritance : multiple susceptibility loci (PSORS1 is the main) • Twin studies : ~73% concordance in monozygotic twins vs. ~20% in dizygotic Environmental • Infections (especially streptococcal for guttate psoriasis) • Certain medications (beta-blockers, lithium, antimalarials) • Stress, smoking, obesity Genetic & Environmental Factors A B PSORIASIS
Variants PSORIASIS Chronic Plaque Psoriasis (psoriasis vulgaris) – 90% of cases Chronic Guttate Erythrodermic PSORIASIS Inverse/flexural Pustural acute onset, small ‘rain-drop’ lesions in skin folds, shiny, less scaling involves >90% BSA, systemic symptoms, emergency generalized or palmoplantar
Chronic Plaque Psoriasis • Well-demarcated, erythematous plaques with silvery scale • Common sites: extensor surfaces (knees, elbows), scalp, lower back • Köbner phenomenon: new plaques at areas of trauma
Guttate and Flexural Psoriasis • Guttate : triggered by strep infections, primarily in children/young adults • Often self-resolving but can evolve into chronic plaque • Flexural (Inverse): older adults, obese patients, minimal scale in folds
Pustular & Erythrodermic Psoriasis • Pustular • Palmoplantar or generalized (von Zumbusch ) • Precipitated by withdrawal of systemic steroids • Erythrodermic • Rare, severe, entire body involvement • Fever, malaise, hemodynamic instability
Nail Psoriasis • Affects ~50% of patients • Pitting , onycholysis, subungual hyperkeratosis, discoloration • Topical treatments often ineffective ; systemic or biologics might help
Assessment & Investigations 04
01 PASI (Psoriasis Area and Severity Index) 02 DLQI (Dermatology Life Quality Index) 03 PEST (Psoriasis Epidemiology Screening Tool) for psoriatic arthritis Assessing Severity & Impact PSORIASIS
Psoriatic Arthritis • Up to 40% with psoriasis may have joint involvement • Ask about joint pain, stiffness, enthesitis • Refer to rheumatology if suspicion • Use PEST or other validated tool
Investigations Clinical diagnosis primarily Screening obesity, metabolic syndrome, depression Biopsy if atypical presentation Blood tests monitoring for comorbidities (lipids, glucose, LFTs if on systemic therapy) 1 4 2 3 PSORIASIS
Topical therapy • First-line for mild disease or localized plaques • Agents : • Vitamin D analogues (calcipotriol) • Potent topical steroids • Coal tar, tazarotene, dithranol (less commonly used now) • Important : watch skin atrophy with long-term steroids
Phototherapy • Narrowband UVB = first choice for moderate-severe psoriasis not controlled by topicals • PUVA (psoralen + UVA) = second-line; watch cumulative dose → skin cancer risk • Typically for widespread or guttate psoriasis
Systemic Therapy • Methotrexate • First-line for moderate-severe psoriasis (PASI >10, DLQI >10) • Weekly dosing, monitor LFTs, FBC, hepatic fibrosis risk • Ciclosporin • Rapid onset, short-term use, monitor renal function, BP • Acitretin • Useful for pustular variants, teratogenic (3-year wait after stopping in women) • Mucocutaneous side effects (dryness, cheilitis)
NICE Key Points on Biologics PSORIASIS • Usually used last-line unless the patient has severe, recalcitrant disease or cannot tolerate non-biologics • Baseline screening for TB, hepatitis • Must consider long-term safety → register patients in BADBIR (British Association of Dermatologists Biological Interventions Register)
Summary of Key Messages • Psoriasis = chronic , systemic inflammatory disease • Variety of clinical patterns → can overlap • NICE : stepped approach from topical to phototherapy to systemic • Monitor for psoriatic arthritis & comorbidities (CV, metabolic, psychological) • Holistic management improves outcomes & quality of life
1. NICE Clinical Guideline CG153 – Psoriasis: assessment and management. National Institute for Health and Care Excellence (2012; last updated 2017). Available at: www.nice.org.uk/guidance/cg153 2. NICE Technology Appraisals – Various TAs on Biological Therapies for Psoriasis. E.g. TA442, TA511, TA521, TA574, etc. Available at: www.nice.org.uk/guidance/conditions-and-diseases/skin-conditions 3. British Association of Dermatologists (BAD) – Guidelines for biologic therapy for psoriasis (including regular updates). Available at: www.bad.org.uk/healthcare-professionals/clinical-standards/clinical-guidelines 4. BNF & BNF for Children – Prescribing guidance on topical and systemic therapies. Available via the NICE BNF portal at: bnf.nice.org.uk 5. Griffiths CEM, Barker JN . Pathogenesis and clinical features of psoriasis. Lancet. 2007; 370(9583): 263–271. 6. Nestle FO, Kaplan DH, Barker J . Psoriasis. N Engl J Med. 2009; 361(5): 496–509. (Seminal paper on immunopathogenesis.) 7. Smith CH, Jabbar-Lopez ZK, Yiu ZZN, et al. British Association of Dermatologists guidelines for biologic therapy for psoriasis 2020: a rapid update. Br J Dermatol. 2020; 183(4): 628–637. 8. Coates LC, Tillett W, Chandler D, et al. Psoriatic arthritis: update on pathophysiology and management. BMJ. 2023; 381: e072286. 9. BADBIR – British Association of Dermatologists Biologic Interventions Register. Available at: www.badbir.org REFERENCES