Cargando…
Dipeptidyl peptidase-4 inhibition and narrow-band ultraviolet-B light in psoriasis (DINUP): study protocol for a randomised controlled trial
BACKGROUND: Moderate to severe psoriasis is a systemic inflammatory disease associated with insulin resistance, obesity and type 2 diabetes (T2DM). Sitagliptin is a dipeptidyl peptidase-4 (DPP-4) inhibitor that improves glycaemia and has a marketing authorisation for the treatment of T2DM. Non-immun...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4714444/ https://www.ncbi.nlm.nih.gov/pubmed/26767505 http://dx.doi.org/10.1186/s13063-016-1157-z |
_version_ | 1782410321644748800 |
---|---|
author | Lynch, Maeve Ahern, Tomás B. Timoney, Irene Sweeney, Cheryl Kelly, Genevieve Hughes, Rosalind Tobin, Anne-Marie O’Shea, Donal Kirby, Brian |
author_facet | Lynch, Maeve Ahern, Tomás B. Timoney, Irene Sweeney, Cheryl Kelly, Genevieve Hughes, Rosalind Tobin, Anne-Marie O’Shea, Donal Kirby, Brian |
author_sort | Lynch, Maeve |
collection | PubMed |
description | BACKGROUND: Moderate to severe psoriasis is a systemic inflammatory disease associated with insulin resistance, obesity and type 2 diabetes (T2DM). Sitagliptin is a dipeptidyl peptidase-4 (DPP-4) inhibitor that improves glycaemia and has a marketing authorisation for the treatment of T2DM. Non-immunosuppressive therapies that are effective for psoriasis and its associated comorbidities would be a significant advance in the treatment of this chronic disease. METHODS/DESIGN: This is a single centre, 39-week, prospective, randomised, open label, clinical trial of oral sitagliptin (Januvia(®)) in psoriasis patients who are due to undergo a course of narrow-band ultraviolet-B (NB-UVB) phototherapy. We plan to enrol 120 participants and allocate participants on a random and 1:1 basis to receive sitagliptin 100 mg daily for 24 weeks combined with NB-UVB or NB-UVB monotherapy. Participants will be followed up for 12 weeks after sitagliptin therapy is discontinued. The primary endpoint is the change in Psoriasis Area and Severity Index (PASI) 24 weeks after treatment initiation. Secondary endpoints include cumulative NB-UVB dose, number of NB-UVB treatments required to clear psoriasis, proportions of participants who achieve PASI-50 (50 % reduction in PASI from baseline), PASI-75, PASI-90 and the proportion of participants who relapse in each group. We will also analyse changes in cardiovascular disease risk factors, serum cytokine and hormone levels and peripheral blood mononuclear expression of immune proteins at 24 and 36 weeks. A subgroup of participants will have skin biopsies taken and analysed for skin levels and expression of immune cells, receptors, hormones and immune proteins. The genetic or epigenetic profile that predicts best response to DPP-4 inhibitor therapy will be analysed. The safety endpoints include the rate and severity of adverse events. DISCUSSION: This is the first randomised clinical trial assessing dipeptidyl peptidase-4 inhibition therapy in psoriasis. We hypothesise that sitagliptin therapy in combination with NB-UVB improves psoriasis severity compared to NB-UVB monotherapy. TRIAL REGISTRATION: ClinicalTrials.gov Identifier NCT02347501 (Date of registration: 27 January 2015). |
format | Online Article Text |
id | pubmed-4714444 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-47144442016-01-16 Dipeptidyl peptidase-4 inhibition and narrow-band ultraviolet-B light in psoriasis (DINUP): study protocol for a randomised controlled trial Lynch, Maeve Ahern, Tomás B. Timoney, Irene Sweeney, Cheryl Kelly, Genevieve Hughes, Rosalind Tobin, Anne-Marie O’Shea, Donal Kirby, Brian Trials Study Protocol BACKGROUND: Moderate to severe psoriasis is a systemic inflammatory disease associated with insulin resistance, obesity and type 2 diabetes (T2DM). Sitagliptin is a dipeptidyl peptidase-4 (DPP-4) inhibitor that improves glycaemia and has a marketing authorisation for the treatment of T2DM. Non-immunosuppressive therapies that are effective for psoriasis and its associated comorbidities would be a significant advance in the treatment of this chronic disease. METHODS/DESIGN: This is a single centre, 39-week, prospective, randomised, open label, clinical trial of oral sitagliptin (Januvia(®)) in psoriasis patients who are due to undergo a course of narrow-band ultraviolet-B (NB-UVB) phototherapy. We plan to enrol 120 participants and allocate participants on a random and 1:1 basis to receive sitagliptin 100 mg daily for 24 weeks combined with NB-UVB or NB-UVB monotherapy. Participants will be followed up for 12 weeks after sitagliptin therapy is discontinued. The primary endpoint is the change in Psoriasis Area and Severity Index (PASI) 24 weeks after treatment initiation. Secondary endpoints include cumulative NB-UVB dose, number of NB-UVB treatments required to clear psoriasis, proportions of participants who achieve PASI-50 (50 % reduction in PASI from baseline), PASI-75, PASI-90 and the proportion of participants who relapse in each group. We will also analyse changes in cardiovascular disease risk factors, serum cytokine and hormone levels and peripheral blood mononuclear expression of immune proteins at 24 and 36 weeks. A subgroup of participants will have skin biopsies taken and analysed for skin levels and expression of immune cells, receptors, hormones and immune proteins. The genetic or epigenetic profile that predicts best response to DPP-4 inhibitor therapy will be analysed. The safety endpoints include the rate and severity of adverse events. DISCUSSION: This is the first randomised clinical trial assessing dipeptidyl peptidase-4 inhibition therapy in psoriasis. We hypothesise that sitagliptin therapy in combination with NB-UVB improves psoriasis severity compared to NB-UVB monotherapy. TRIAL REGISTRATION: ClinicalTrials.gov Identifier NCT02347501 (Date of registration: 27 January 2015). BioMed Central 2016-01-15 /pmc/articles/PMC4714444/ /pubmed/26767505 http://dx.doi.org/10.1186/s13063-016-1157-z Text en © Lynch et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Study Protocol Lynch, Maeve Ahern, Tomás B. Timoney, Irene Sweeney, Cheryl Kelly, Genevieve Hughes, Rosalind Tobin, Anne-Marie O’Shea, Donal Kirby, Brian Dipeptidyl peptidase-4 inhibition and narrow-band ultraviolet-B light in psoriasis (DINUP): study protocol for a randomised controlled trial |
title | Dipeptidyl peptidase-4 inhibition and narrow-band ultraviolet-B light in psoriasis (DINUP): study protocol for a randomised controlled trial |
title_full | Dipeptidyl peptidase-4 inhibition and narrow-band ultraviolet-B light in psoriasis (DINUP): study protocol for a randomised controlled trial |
title_fullStr | Dipeptidyl peptidase-4 inhibition and narrow-band ultraviolet-B light in psoriasis (DINUP): study protocol for a randomised controlled trial |
title_full_unstemmed | Dipeptidyl peptidase-4 inhibition and narrow-band ultraviolet-B light in psoriasis (DINUP): study protocol for a randomised controlled trial |
title_short | Dipeptidyl peptidase-4 inhibition and narrow-band ultraviolet-B light in psoriasis (DINUP): study protocol for a randomised controlled trial |
title_sort | dipeptidyl peptidase-4 inhibition and narrow-band ultraviolet-b light in psoriasis (dinup): study protocol for a randomised controlled trial |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4714444/ https://www.ncbi.nlm.nih.gov/pubmed/26767505 http://dx.doi.org/10.1186/s13063-016-1157-z |
work_keys_str_mv | AT lynchmaeve dipeptidylpeptidase4inhibitionandnarrowbandultravioletblightinpsoriasisdinupstudyprotocolforarandomisedcontrolledtrial AT aherntomasb dipeptidylpeptidase4inhibitionandnarrowbandultravioletblightinpsoriasisdinupstudyprotocolforarandomisedcontrolledtrial AT timoneyirene dipeptidylpeptidase4inhibitionandnarrowbandultravioletblightinpsoriasisdinupstudyprotocolforarandomisedcontrolledtrial AT sweeneycheryl dipeptidylpeptidase4inhibitionandnarrowbandultravioletblightinpsoriasisdinupstudyprotocolforarandomisedcontrolledtrial AT kellygenevieve dipeptidylpeptidase4inhibitionandnarrowbandultravioletblightinpsoriasisdinupstudyprotocolforarandomisedcontrolledtrial AT hughesrosalind dipeptidylpeptidase4inhibitionandnarrowbandultravioletblightinpsoriasisdinupstudyprotocolforarandomisedcontrolledtrial AT tobinannemarie dipeptidylpeptidase4inhibitionandnarrowbandultravioletblightinpsoriasisdinupstudyprotocolforarandomisedcontrolledtrial AT osheadonal dipeptidylpeptidase4inhibitionandnarrowbandultravioletblightinpsoriasisdinupstudyprotocolforarandomisedcontrolledtrial AT kirbybrian dipeptidylpeptidase4inhibitionandnarrowbandultravioletblightinpsoriasisdinupstudyprotocolforarandomisedcontrolledtrial |