Comparison of Topical Mometasone vs Topical Beclomethasone
Mometasone furoate is the superior choice over beclomethasone for inflammatory skin conditions, offering comparable or better efficacy with once-daily dosing, lower systemic absorption (0.7% bioavailability), and reduced risk of HPA axis suppression. 1, 2
Potency Classification
- Mometasone furoate 0.1% is classified as a medium-potency (Class IV) topical corticosteroid with strong anti-inflammatory activity 3, 1
- Mometasone is a synthetic 16-alpha-methyl analogue of beclomethasone, specifically engineered to enhance topical potency while minimizing systemic effects 2
- The vasoconstrictor assay demonstrates strong blanching effects, confirming high topical bioavailability of the active ingredient 4
Efficacy Comparison
Atopic Dermatitis & Eczema
- Mometasone 0.1% once daily produces equivalent results to betamethasone dipropionate 0.05% twice daily over 2-3 weeks 2
- In direct comparison, mometasone 0.1% once daily achieved 93.6% improvement versus betamethasone valerate 0.1% twice daily at 96.5% improvement after 21 days—clinically equivalent outcomes with half the application frequency 5
- Mometasone significantly outperforms lower-potency agents including hydrocortisone 1.0%, clobetasone 0.05%, and hydrocortisone butyrate 2
Psoriasis
- For plaque psoriasis, mometasone demonstrates superior efficacy compared to betamethasone valerate 0.1%, fluocinolone acetonide 0.025%, and triamcinolone acetonide 0.1% 2
- The psoriasis plaque test shows strong antipsoriatic effects with nearly identical reduction in mean infiltrate thickness compared to fatty cream formulations 4
- Mometasone is effective for scalp psoriasis when applied once daily for 2-8 weeks 2
Seborrheic Dermatitis
- Mometasone 0.1% proves more effective than ketoconazole 2.0% and hydrocortisone 1.0% in 4-6 week trials 2
Safety Profile
Systemic Absorption
- Mometasone has minimal percutaneous absorption at approximately 0.7% of applied dose entering circulation after 8 hours on normal skin without occlusion 1
- This represents approximately half the HPA axis suppression potential of betamethasone valerate 2, 6
Skin Atrophy Risk
- Mometasone and betamethasone-17-valerate decrease collagen synthesis to similar extents in human skin, indicating comparable atrophogenic potential within the same potency class 7
- The atrophogenic potential is low and no greater than other glucocorticoids in its class 2
Pediatric Considerations
- In pediatric patients ages 6-23 months with atopic dermatitis, approximately 29% showed adrenal suppression when mometasone was applied once daily over mean body surface area of 40% for 3 weeks 1
- Follow-up testing 2-4 weeks after stopping treatment showed recovery in most patients, with only 1 of 8 tested patients demonstrating persistent suppression 1
Dosing Advantages
- Mometasone requires only once-daily application versus twice-daily for most comparator steroids, improving adherence while maintaining equivalent efficacy 2, 5
- For maintenance therapy in eczema, mometasone applied twice weekly to previously affected areas for up to 36 weeks achieves 68% remission rate 3
- Alternate-day application maintains symptom control in psoriasis vulgaris patients 2
Formulation Options
- Available as 0.1% cream, ointment, and lotion formulations for different clinical scenarios 1, 2
- The light cream formulation (O/W 60/40 emulsion) is particularly suitable for acutely inflamed and sensitive skin 4
Common Pitfalls to Avoid
- Do not use on face, intertriginous areas, or areas susceptible to steroid atrophy without careful monitoring 8
- Avoid occlusive dressings beyond 24 hours, as 96-hour occlusion markedly enhances penetration and systemic absorption 1
- Reassess after 2-4 weeks to determine if continued treatment is necessary and consider step-down to lower potency agents once control is achieved 8
Clinical Bottom Line
Mometasone furoate 0.1% once daily is the preferred agent over beclomethasone-derived products for most inflammatory dermatoses, offering superior convenience, comparable efficacy to higher-frequency betamethasone regimens, and a favorable safety profile with low systemic bioavailability. 1, 2, 5