Sitagliptin and Narrow-Band Ultraviolet-B for Moderate Psoriasis (DINUP): A Randomised Controlled Clinical Trial.


Journal

Dermatology (Basel, Switzerland)
ISSN: 1421-9832
Titre abrégé: Dermatology
Pays: Switzerland
ID NLM: 9203244

Informations de publication

Date de publication:
2022
Historique:
received: 04 08 2020
accepted: 17 01 2021
pubmed: 19 4 2021
medline: 26 2 2022
entrez: 18 4 2021
Statut: ppublish

Résumé

Sitagliptin, a dipeptidyl peptidase-4 (DPP-4) inhibitor licensed for the treatment of type 2 diabetes mellitus (T2DM), has been reported to improve psoriasis. We compared the effects of sitagliptin treatment, a DPP-4 inhibitor, in combination with narrow-band ultraviolet-B (NB-UVB) phototherapy compared to NB-UVB alone on psoriasis severity, quality of life, cardiovascular disease risk factors and immune parameters in people with moderate psoriasis without T2DM. In this 39-week, single-centre, randomised controlled trial, people were allocated randomly to receive sitagliptin for 24 weeks with NB-UVB or NB-UVB alone. The primary endpoint was the change in Psoriasis Area and Severity Index (PASI) from baseline to 24 weeks. We estimated that 120 participants would be needed to have 80% power to find a significant difference between the groups. A total of 118 patients were randomised. The median (IQR) baseline PASI was 8.8 (7.5-11.6). At 24 weeks, the mean difference from baseline in PASI (-1.0 [95% CI -2.0 to 0.0]) was significantly larger in the sitagliptin/NB-UVB arm than in the NB-UVB-alone arm (p = 0.044). There were significant differences in the change in Hospital Anxiety and Depression Scale (-2.5 [95% CI -4.0 to -1.0]; p = 0.002) and EuroQol 5-item questionnaire (0.1 [95% CI 0.0-0.1]; p = 0.036) values from baseline to 24 weeks between the sitagliptin/NB-UVB and the NB-UVB-alone arm. There were no treatment-related serious adverse events. Sitagliptin therapy combined with NB-UVB phototherapy significantly improved psoriasis severity, albeit modestly, compared to NB-UVB phototherapy alone in patients with moderate psoriasis without T2DM.

Sections du résumé

BACKGROUND BACKGROUND
Sitagliptin, a dipeptidyl peptidase-4 (DPP-4) inhibitor licensed for the treatment of type 2 diabetes mellitus (T2DM), has been reported to improve psoriasis.
OBJECTIVE OBJECTIVE
We compared the effects of sitagliptin treatment, a DPP-4 inhibitor, in combination with narrow-band ultraviolet-B (NB-UVB) phototherapy compared to NB-UVB alone on psoriasis severity, quality of life, cardiovascular disease risk factors and immune parameters in people with moderate psoriasis without T2DM.
METHODS METHODS
In this 39-week, single-centre, randomised controlled trial, people were allocated randomly to receive sitagliptin for 24 weeks with NB-UVB or NB-UVB alone. The primary endpoint was the change in Psoriasis Area and Severity Index (PASI) from baseline to 24 weeks. We estimated that 120 participants would be needed to have 80% power to find a significant difference between the groups.
RESULTS RESULTS
A total of 118 patients were randomised. The median (IQR) baseline PASI was 8.8 (7.5-11.6). At 24 weeks, the mean difference from baseline in PASI (-1.0 [95% CI -2.0 to 0.0]) was significantly larger in the sitagliptin/NB-UVB arm than in the NB-UVB-alone arm (p = 0.044). There were significant differences in the change in Hospital Anxiety and Depression Scale (-2.5 [95% CI -4.0 to -1.0]; p = 0.002) and EuroQol 5-item questionnaire (0.1 [95% CI 0.0-0.1]; p = 0.036) values from baseline to 24 weeks between the sitagliptin/NB-UVB and the NB-UVB-alone arm. There were no treatment-related serious adverse events.
CONCLUSION CONCLUSIONS
Sitagliptin therapy combined with NB-UVB phototherapy significantly improved psoriasis severity, albeit modestly, compared to NB-UVB phototherapy alone in patients with moderate psoriasis without T2DM.

Identifiants

pubmed: 33866313
pii: 000514494
doi: 10.1159/000514494
doi:

Substances chimiques

Dipeptidyl-Peptidase IV Inhibitors 0
Sitagliptin Phosphate TS63EW8X6F

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

140-147

Informations de copyright

© 2021 S. Karger AG, Basel.

Auteurs

Maeve Lynch (M)

Charles Department of Dermatology, St Vincent's University Hospital, Dublin, Ireland.
School of Health Sciences and Charles Institute, University College Dublin, Dublin, Ireland.

Anna Malara (A)

School of Health Sciences and Charles Institute, University College Dublin, Dublin, Ireland.

Irene Timoney (I)

Charles Department of Dermatology, St Vincent's University Hospital, Dublin, Ireland.

Sebastian Vencken (S)

Clinical Research Centre, University College Dublin, Dublin, Ireland.

Tomas Ahern (T)

Department of Endocrinology, St Vincent's University Hospital, Dublin, Ireland.

Fatima Awdeh (F)

Charles Department of Dermatology, St Vincent's University Hospital, Dublin, Ireland.

Cheryl Sweeney (C)

School of Health Sciences and Charles Institute, University College Dublin, Dublin, Ireland.

Marie Galligan (M)

Clinical Research Centre, University College Dublin, Dublin, Ireland.

Genevieve Kelly (G)

Charles Department of Dermatology, St Vincent's University Hospital, Dublin, Ireland.

Rosalind Hughes (R)

Charles Department of Dermatology, St Vincent's University Hospital, Dublin, Ireland.

Aizuri Murad (A)

Charles Department of Dermatology, St Vincent's University Hospital, Dublin, Ireland.

Roisin Hambly (R)

Charles Department of Dermatology, St Vincent's University Hospital, Dublin, Ireland.

Donal O'Shea (D)

School of Health Sciences and Charles Institute, University College Dublin, Dublin, Ireland.
Department of Endocrinology, St Vincent's University Hospital, Dublin, Ireland.

Peter Doran (P)

Clinical Research Centre, University College Dublin, Dublin, Ireland.

Brian Kirby (B)

Charles Department of Dermatology, St Vincent's University Hospital, Dublin, Ireland.
School of Health Sciences and Charles Institute, University College Dublin, Dublin, Ireland.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH