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1.
PLoS One ; 10(8): e0137133, 2015.
Article in English | MEDLINE | ID: mdl-26318001

ABSTRACT

Diabetes Mellitus (DM) is a chronic, severe disease rapidly increasing in incidence and prevalence and is associated with numerous complications. Patients with DM are at high risk of developing diabetic foot ulcers (DFU) that often lead to lower limb amputations, long term disability, and a shortened lifespan. Despite this, the effects of DM on human foot skin biology are largely unknown. Thus, the focus of this study was to determine whether DM changes foot skin biology predisposing it for healing impairment and development of DFU. Foot skin samples were collected from 20 patients receiving corrective foot surgery and, using a combination of multiple molecular and cellular approaches, we performed comparative analyses of non-ulcerated non-neuropathic diabetic foot skin (DFS) and healthy non-diabetic foot skin (NFS). MicroRNA (miR) profiling of laser captured epidermis and primary dermal fibroblasts from both DFS and NFS samples identified 5 miRs de-regulated in the epidermis of DFS though none reached statistical significance. MiR-31-5p and miR-31-3p were most profoundly induced. Although none were significantly regulated in diabetic fibroblasts, miR-29c-3p showed a trend of up-regulation, which was confirmed by qPCR in a prospective set of 20 skin samples. Gene expression profiling of full thickness biopsies identified 36 de-regulated genes in DFS (>2 fold-change, unadjusted p-value ≤ 0.05). Of this group, three out of seven tested genes were confirmed by qPCR: SERPINB3 was up-regulated whereas OR2A4 and LGR5 were down-regulated in DFS. However no morphological differences in histology, collagen deposition, and number of blood vessels or lymphocytes were found. No difference in proliferative capacity was observed by quantification of Ki67 positive cells in epidermis. These findings suggest DM causes only subtle changes to foot skin. Since morphology, mRNA and miR levels were not affected in a major way, additional factors, such as neuropathy, vascular complications, or duration of DM, may further compromise tissue's healing ability leading to development of DFUs.


Subject(s)
Dermis/pathology , Diabetic Foot/genetics , Diabetic Foot/pathology , Epidermis/pathology , Genomics , MicroRNAs/genetics , Fibroblasts/metabolism , Foot Ulcer/genetics , Foot Ulcer/pathology , Gene Expression Profiling , Humans , Transcription, Genetic
2.
Hosp Pract (1995) ; 40(3): 102-15, 2012 Aug.
Article in English | MEDLINE | ID: mdl-23086099

ABSTRACT

Diabetic foot ulcers (DFUs) are a common complication of diabetes and present a significant health risk to patients, as well as impose a large economic burden. Evaluation for contributory factors that may impact general health or healing, such as hyperglycemia, peripheral artery disease, neuropathy, and nutritional status, is of the utmost importance. Management of DFUs requires involvement of a multidisciplinary team and a standardized approach to patient care. Standard therapy for DFUs includes offloading and debridement. Assessment and control of infection are critical, including determining the severity of the infection, which may drive therapeutic approaches. For recalcitrant ulcers, adjuvant therapies are used to hasten the healing process, and newer therapies are under investigation.


Subject(s)
Diabetic Foot/therapy , Amputation, Surgical , Anti-Infective Agents/therapeutic use , Bandages , Cell- and Tissue-Based Therapy , Chemotherapy, Adjuvant , Debridement/methods , Diabetic Foot/etiology , Diabetic Neuropathies/complications , Humans , Hyperbaric Oxygenation , Negative-Pressure Wound Therapy , Nutritional Status , Osteomyelitis/etiology , Peripheral Vascular Diseases/complications , Risk Factors , Stem Cell Transplantation
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