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| Research article summary (published 29 Sep 2009): |
Heat-shock protein 70 gene polymorphism is associated with the severity of diabetic foot ulcer and the outcome of surgical treatment.
Full Abstract
BACKGROUND: Foot ulcer is a significant cause of morbidity in diabetics. Genetic make-up can determine inflammatory and healing responses. This study examined the hypothesis that specific polymorphisms of the heat-shock protein 70 gene could predispose to the severity of diabetic foot ulceration. METHODS: Some 106 consecutive diabetic patients (101 evaluable) with foot ulceration admitted to a tertiary care hospital were managed according to a standard protocol. DNA was extracted from venous blood and examined by polymerase chain reaction-restriction fragment length analysis for two specific polymorphisms: G1538A in the HSPA1B and C2437T in the HSPA1L gene. RESULTS: HSPA1B genotyping showed that 70 patients were AG and 30 GG (one not amplified). The AG genotype was significantly associated with the severity of foot ulceration (Wagner grade) (P = 0.008, chi(2) test), need for amputation (relative risk 2.02, 95 per cent confidence interval 1.02 to 4.01; P = 0.025) and median length of hospital stay (8 versus 5 days for GG; P = 0.043). HSPA1L genotypes (78 TT, 22 CT, one CC) did not show any significant association with these parameters. CONCLUSION: The HSPA1B genotype, was associated with the severity of diabetic foot ulceration, need for amputation and duration of hospitalization in these patients.
Author information
Author/s: Mir, K A (KA); Pugazhendhi, S (S); Paul, M J (MJ); Nair, A (A); Ramakrishna, B S (BS);
Affiliation: Department of Surgical Endocrinology, Christian Medical College, Vellore, India.
Journal and publication information
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal: The British journal of surgery (Br J Surg), published in England. (Language: eng)
Reference: 2009-Oct; vol 96 (issue 10) : pp 1205-9
Dates: Created 2009/10/05; Completed 2009/10/29;
PMID: 19731315, status: MEDLINE (last retrieval date: 10/29/2009, IMS Date: )
Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.
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