Literature DB >> 17552400

Effect of amelogenin extracellular matrix protein and compression on hard-to-heal venous leg ulcers.

P Vowden1, M Romanelli, P Price.   

Abstract

OBJECTIVE: To compare hard-to-heal venous leg ulcers treated with compression therapy alone versus compression therapy with amelogenin protein. Parameters used were: percentage reduction in wound size, number of improved ulcers, pain related to the disease and at dressing changes, amount and nature of exudate, and the safety and tolerability of the two treatments.
METHOD: This was an open randomised comparative parallel group multicentre investigation with a three-week run-in period. Inclusion criteria included adult, mobile patients with hard-to-heal venous leg ulcers that had been treated with compression therapy for at least one month prior to screening. The ulcers had to be at least six months old, with a surface area at inclusion of 10-30cm2, and not demonstrating excessive exudate or signs of infection. At the end of the run-in period, additional criteria for eligibility, such as change in wound area of +/- > or = 50% and a wound area between 8cm2 and 36cm2 were applied. Patients were randomised to treatment with amelogenin plus high compression bandaging or high compression bandaging alone. All participants received high compression bandaging therapy one month prior to and during the three-week run-in period, as well as throughout the 12 weeks of active treatment.
RESULTS: Eighty-three patients were randomised and received treatment: 42 with high compression plus amelogenin (amelogenin group) and 41 to high compression therapy alone (control group). The amelogenin group had a greater percentage reduction in ulcer size (mean - 33.1%) compared with the control group (mean - 11.07%) from baseline to the last visit (p = 0.06). The number of improved ulcers was significantly greater (p = 0.01) in the amelogenin group than in the control group. Compensating for baseline characteristics by multiple regression resulted in a statistically significant (p = 0.03) larger reduction in change in ulcer size in the amelogenin group. Statistically significant differences in favour of the amelogenin group were also found for reduction in ulcer-related pain (p = 0.01), reduction in pain at dressing changes (p = 0.02) and the proportion of patients with 'none' or 'low' levels of exudate (p = 0.01).
CONCLUSION: The combination of amelogenin with high compression promotes the healing process in hard-to-heal ulcers. Application of amelogenin as an adjunct to compression results in a significant reduction in ulcer size, improvement in the state of ulcers, reduced pain and a larger proportion of ulcers with low levels of exudate. The results of this study are statistically and clinically significant.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17552400     DOI: 10.12968/jowc.2007.16.5.27043

Source DB:  PubMed          Journal:  J Wound Care        ISSN: 0969-0700            Impact factor:   2.072


  9 in total

1.  Amelogenin is phagocytized and induces changes in integrin configuration, gene expression and proliferation of cultured normal human dermal fibroblasts.

Authors:  Sofia Almqvist; Maria Werthén; Anna Johansson; Magnus S Agren; Peter Thomsen; S Petter Lyngstadaas
Journal:  J Mater Sci Mater Med       Date:  2009-12-10       Impact factor: 3.896

2.  Effectiveness of an acellular synthetic matrix in the treatment of hard-to-heal leg ulcers.

Authors:  Keith Harding; Pat Aldons; Helen Edwards; Michael Stacey; Kathleen Finlayson; Michelle Gibb; Liz Jenkins; Gary Shooter; Derek Van Lonkhuyzen; Emily Lynam; Eva-Lisa Heinrichs; Zee Upton
Journal:  Int Wound J       Date:  2013-07-09       Impact factor: 3.315

3.  Expression of amelogenin and effects of cyclosporin A in developing hair follicles in rats.

Authors:  Hong-Il Yoo; Gye-Hyeok Lee; Su-Young Lee; Jee-Hae Kang; Jung-Sun Moon; Min-Seok Kim; Sun-Hun Kim
Journal:  J Anat       Date:  2015-10-01       Impact factor: 2.610

4.  Protocol for a pilot randomised controlled clinical trial to compare the effectiveness of a graduated three layer straight tubular bandaging system when compared to a standard short stretch compression bandaging system in the management of people with venous ulceration: 3VSS2008.

Authors:  Carolina D Weller; Sue Evans; Christopher M Reid; Rory Wolfe; John McNeil
Journal:  Trials       Date:  2010-03-09       Impact factor: 2.279

Review 5.  Enamel matrix proteins; old molecules for new applications.

Authors:  S P Lyngstadaas; J C Wohlfahrt; S J Brookes; M L Paine; M L Snead; J E Reseland
Journal:  Orthod Craniofac Res       Date:  2009-08       Impact factor: 1.826

6.  Enamel matrix derivative improves gingival fibroblast cell behavior cultured on titanium surfaces.

Authors:  Yulan Wang; Yufeng Zhang; Dai Jing; Yang Shuang; Richard J Miron
Journal:  Clin Oral Investig       Date:  2015-08-14       Impact factor: 3.573

Review 7.  Protease-modulating matrix treatments for healing venous leg ulcers.

Authors:  Maggie J Westby; Gill Norman; Jo C Dumville; Nikki Stubbs; Nicky Cullum
Journal:  Cochrane Database Syst Rev       Date:  2016-12-15

Review 8.  Dressings and topical agents for treating venous leg ulcers.

Authors:  Gill Norman; Maggie J Westby; Amber D Rithalia; Nikki Stubbs; Marta O Soares; Jo C Dumville
Journal:  Cochrane Database Syst Rev       Date:  2018-06-15

Review 9.  Amelogenin, an extracellular matrix protein, in the treatment of venous leg ulcers and other hard-to-heal wounds: experimental and clinical evidence.

Authors:  Marco Romanelli; Valentina Dini; Peter Vowden; Magnus S Agren
Journal:  Clin Interv Aging       Date:  2008       Impact factor: 4.458

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.