Increased Matrix Metalloproteinase-9 Predicts Poor Wound Healing in Diabetic Foot Ulcers

OBJECTIVE—We studied the relationships of diabetic ulcer wound fluid matrix metalloproteinases (MMPs), tissue inhibitors of metalloproteinases (TIMPs), and transforming growth factor-ß1 (TGF-ß1) with wound healing rate. RESEARCH DESIGN AND METHODS—The ulcers were cleansed to remove exudates, and wound fluids were collected for analysis of MMP-2 and -9, TIMP-1, and TGF-ß1. RESULTS—At presentation, MMP-9 and the MMP-9–to–TIMP-1 ratio correlated inversely with the wound healing rate at 28 days (P < 0.001). MMP-9 and the MMP-9–to–TIMP-1 ratio were lower in the 23 patients who achieved complete healing at 12 weeks versus the 39 who did not. The pro–MMP-9 concentration was predictive of healing within 12 weeks. Addition of cutoffs for TIMP-1 (>480 pg/ml) and TGF-ß (>115 pg/ml) further improved its predictive power (area under the curve 0.94). CONCLUSIONS—These findings suggest that a milieu with high MMP-9 may be indicative of inflammation and poor wound healing. Measurements of MMP-9, TIMP-1, and TGF-ß in wound fluid may help to identify ulcers at risk of poor healing.

[1]  C. Bachert,et al.  Predictive and monitoring value of matrix metalloproteinase‐9 for healing quality after sinus surgery , 2004, Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society.

[2]  Paul G Scott,et al.  Pathophysiology of chronic nonhealing wounds. , 2005, The Journal of burn care & rehabilitation.

[3]  I Tarawneh,et al.  The effects of ulcer size and site, patient's age, sex and type and duration of diabetes on the outcome of diabetic foot ulcers , 2001, Diabetic medicine : a journal of the British Diabetic Association.

[4]  Andrew J.M. Boulton,et al.  Neuropathic Diabetic Foot Ulcers , 2004 .

[5]  H. Lehnert,et al.  Expression of matrix metalloproteinases and growth factors in diabetic foot wounds treated with a protease absorbent dressing. , 2006, Journal of diabetes and its complications.

[6]  Vincent Falanga,et al.  Wound healing and its impairment in the diabetic foot , 2005, The Lancet.

[7]  J. Kere,et al.  Patterns of matrix metalloproteinase and TIMP‐1 expression in chronic and normally healing human cutaneous wounds , 1996, The British journal of dermatology.

[8]  S. Mclennan,et al.  2‐Methoxy‐2,4‐diphenyl‐3(2H)‐furanone‐labeled gelatin zymography and reverse zymography: A rapid real‐time method for quantification of matrix metalloproteinases‐2 and ‐9 and tissue inhibitors of metalloproteinases , 2006, Electrophoresis.

[9]  S. Werner,et al.  Matrix metalloproteinases (MMPs) and their physiological inhibitors (TIMPs) are differentially expressed during excisional skin wound repair. , 1998, Experimental cell research.

[10]  H. Lehnert,et al.  Expression of matrix-metalloproteinases and their inhibitors in the wounds of diabetic and non-diabetic patients , 2002, Diabetologia.

[11]  W. Parks Matrix metalloproteinases in repair , 1999, Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society.

[12]  M. Longaker,et al.  Differential Expression of Matrix Metalloproteinases and Their Tissue-Derived Inhibitors in Cutaneous Wound Repair , 2000, Plastic and reconstructive surgery.