Hardness of Plantar Skin in Diabetic Neuropathic Feet
To evaluate if skin hardness in diabetic neuropathic feet was increased and if its eventual modifications could be correlated to the severity of neuropathy, we studied a group of diabetic outpatients with and without neuropathy. Patients, selected among those who were attending their routine screeni...
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Veröffentlicht in: | Journal of diabetes and its complications 1999-05, Vol.13 (3), p.129-134 |
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description | To evaluate if skin hardness in diabetic neuropathic feet was increased and if its eventual modifications could be correlated to the severity of neuropathy, we studied a group of diabetic outpatients with and without neuropathy. Patients, selected among those who were attending their routine screening for diabetic neuropathy at our diabetologic clinic, were divided into two groups according to the presence (ND+) or absence (ND−) of diabetic neuropathy with the criteria of the S. Antonio Consensus Conference on Diabetic Neuropathy. Patients then underwent an evaluation of vibration perception threshold (VPT) by means of a biotesiometer, measurement of skin hardness (DMT) by means of a durometer, and transcutaneous oxygen tension (TcPO2) determination. VPT was determined at allux (VPT-A) and external malleolus (VPT-M), DMT was measured at heel (DMT-H), at medial (DMT-M) and lateral (DMT-L) midfoot, and at posterior midcalf (DTM-C) as a control site; TcPO2 was evaluated at dorsum (TcPO2-D) and at medial midfoot (TcPO2-M), respectively. All measurements were performed on the nondominant side with the patients supine. Patients were compared with age and gender-matched healthy volunteers (Controls), who underwent the same evaluations in the same order. ND+ patients showed higher values of VPT than ND− and Controls, both at first toe and at malleolus analysis of variance (ANOVA) p < 0.01), as well of DMT in all the three sites explored (ANOVA, p < 0.01). Moreover, ND+ showed no difference in DMT among the sites, while both in ND− and in controls DMT-M was significantly (p < 0.05) lower than DMT-H and DMT-L. No difference among the three groups were observed in TcPO2 measurements, and no difference in DMT-C was observed either. A significant correlation was observed between DMT-H and VPT-M (r2 = 0.516) and between DMT-M and VPT-A (r2 = 0.624) in ND+ patients. Skin hardness was diffusely increased in ND+ patients, and this increase strongly correlates with the severity of neuropathy. Simple, noninvasive determination of skin hardness could identify patient at potential risk to develop neuropathic foot ulcers. |
doi_str_mv | 10.1016/S1056-8727(98)00022-1 |
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Patients, selected among those who were attending their routine screening for diabetic neuropathy at our diabetologic clinic, were divided into two groups according to the presence (ND+) or absence (ND−) of diabetic neuropathy with the criteria of the S. Antonio Consensus Conference on Diabetic Neuropathy. Patients then underwent an evaluation of vibration perception threshold (VPT) by means of a biotesiometer, measurement of skin hardness (DMT) by means of a durometer, and transcutaneous oxygen tension (TcPO2) determination. VPT was determined at allux (VPT-A) and external malleolus (VPT-M), DMT was measured at heel (DMT-H), at medial (DMT-M) and lateral (DMT-L) midfoot, and at posterior midcalf (DTM-C) as a control site; TcPO2 was evaluated at dorsum (TcPO2-D) and at medial midfoot (TcPO2-M), respectively. All measurements were performed on the nondominant side with the patients supine. Patients were compared with age and gender-matched healthy volunteers (Controls), who underwent the same evaluations in the same order. ND+ patients showed higher values of VPT than ND− and Controls, both at first toe and at malleolus analysis of variance (ANOVA) p < 0.01), as well of DMT in all the three sites explored (ANOVA, p < 0.01). Moreover, ND+ showed no difference in DMT among the sites, while both in ND− and in controls DMT-M was significantly (p < 0.05) lower than DMT-H and DMT-L. No difference among the three groups were observed in TcPO2 measurements, and no difference in DMT-C was observed either. A significant correlation was observed between DMT-H and VPT-M (r2 = 0.516) and between DMT-M and VPT-A (r2 = 0.624) in ND+ patients. Skin hardness was diffusely increased in ND+ patients, and this increase strongly correlates with the severity of neuropathy. Simple, noninvasive determination of skin hardness could identify patient at potential risk to develop neuropathic foot ulcers.</description><identifier>ISSN: 1056-8727</identifier><identifier>EISSN: 1873-460X</identifier><identifier>DOI: 10.1016/S1056-8727(98)00022-1</identifier><identifier>PMID: 10509872</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Adult ; Associated diseases and complications ; Biological and medical sciences ; Blood Gas Monitoring, Transcutaneous ; Diabetes. Impaired glucose tolerance ; Diabetic Foot - diagnosis ; Diabetic Foot - physiopathology ; Diabetic Neuropathies - physiopathology ; Endocrine pancreas. Apud cells (diseases) ; Endocrinopathies ; Female ; Humans ; Male ; Medical sciences ; Middle Aged ; Perception ; Skin - physiopathology ; Vibration</subject><ispartof>Journal of diabetes and its complications, 1999-05, Vol.13 (3), p.129-134</ispartof><rights>1999 Elsevier Science Inc.</rights><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c447t-b15aa1fa8c151527243a7d898b44e2dafc8429e08ea1cf4bf722857fd09eb1cf3</citedby><cites>FETCH-LOGICAL-c447t-b15aa1fa8c151527243a7d898b44e2dafc8429e08ea1cf4bf722857fd09eb1cf3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1056872798000221$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1987944$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10509872$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Piaggesi, Alberto</creatorcontrib><creatorcontrib>Romanelli, Marco</creatorcontrib><creatorcontrib>Schipani, Elena</creatorcontrib><creatorcontrib>Campi, Fabrizio</creatorcontrib><creatorcontrib>Magliaro, Antonio</creatorcontrib><creatorcontrib>Baccetti, Fabio</creatorcontrib><creatorcontrib>Navalesi, Renzo</creatorcontrib><title>Hardness of Plantar Skin in Diabetic Neuropathic Feet</title><title>Journal of diabetes and its complications</title><addtitle>J Diabetes Complications</addtitle><description>To evaluate if skin hardness in diabetic neuropathic feet was increased and if its eventual modifications could be correlated to the severity of neuropathy, we studied a group of diabetic outpatients with and without neuropathy. Patients, selected among those who were attending their routine screening for diabetic neuropathy at our diabetologic clinic, were divided into two groups according to the presence (ND+) or absence (ND−) of diabetic neuropathy with the criteria of the S. Antonio Consensus Conference on Diabetic Neuropathy. Patients then underwent an evaluation of vibration perception threshold (VPT) by means of a biotesiometer, measurement of skin hardness (DMT) by means of a durometer, and transcutaneous oxygen tension (TcPO2) determination. VPT was determined at allux (VPT-A) and external malleolus (VPT-M), DMT was measured at heel (DMT-H), at medial (DMT-M) and lateral (DMT-L) midfoot, and at posterior midcalf (DTM-C) as a control site; TcPO2 was evaluated at dorsum (TcPO2-D) and at medial midfoot (TcPO2-M), respectively. All measurements were performed on the nondominant side with the patients supine. Patients were compared with age and gender-matched healthy volunteers (Controls), who underwent the same evaluations in the same order. ND+ patients showed higher values of VPT than ND− and Controls, both at first toe and at malleolus analysis of variance (ANOVA) p < 0.01), as well of DMT in all the three sites explored (ANOVA, p < 0.01). Moreover, ND+ showed no difference in DMT among the sites, while both in ND− and in controls DMT-M was significantly (p < 0.05) lower than DMT-H and DMT-L. No difference among the three groups were observed in TcPO2 measurements, and no difference in DMT-C was observed either. A significant correlation was observed between DMT-H and VPT-M (r2 = 0.516) and between DMT-M and VPT-A (r2 = 0.624) in ND+ patients. Skin hardness was diffusely increased in ND+ patients, and this increase strongly correlates with the severity of neuropathy. 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Impaired glucose tolerance</topic><topic>Diabetic Foot - diagnosis</topic><topic>Diabetic Foot - physiopathology</topic><topic>Diabetic Neuropathies - physiopathology</topic><topic>Endocrine pancreas. 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Patients, selected among those who were attending their routine screening for diabetic neuropathy at our diabetologic clinic, were divided into two groups according to the presence (ND+) or absence (ND−) of diabetic neuropathy with the criteria of the S. Antonio Consensus Conference on Diabetic Neuropathy. Patients then underwent an evaluation of vibration perception threshold (VPT) by means of a biotesiometer, measurement of skin hardness (DMT) by means of a durometer, and transcutaneous oxygen tension (TcPO2) determination. VPT was determined at allux (VPT-A) and external malleolus (VPT-M), DMT was measured at heel (DMT-H), at medial (DMT-M) and lateral (DMT-L) midfoot, and at posterior midcalf (DTM-C) as a control site; TcPO2 was evaluated at dorsum (TcPO2-D) and at medial midfoot (TcPO2-M), respectively. All measurements were performed on the nondominant side with the patients supine. Patients were compared with age and gender-matched healthy volunteers (Controls), who underwent the same evaluations in the same order. ND+ patients showed higher values of VPT than ND− and Controls, both at first toe and at malleolus analysis of variance (ANOVA) p < 0.01), as well of DMT in all the three sites explored (ANOVA, p < 0.01). Moreover, ND+ showed no difference in DMT among the sites, while both in ND− and in controls DMT-M was significantly (p < 0.05) lower than DMT-H and DMT-L. No difference among the three groups were observed in TcPO2 measurements, and no difference in DMT-C was observed either. A significant correlation was observed between DMT-H and VPT-M (r2 = 0.516) and between DMT-M and VPT-A (r2 = 0.624) in ND+ patients. Skin hardness was diffusely increased in ND+ patients, and this increase strongly correlates with the severity of neuropathy. Simple, noninvasive determination of skin hardness could identify patient at potential risk to develop neuropathic foot ulcers.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>10509872</pmid><doi>10.1016/S1056-8727(98)00022-1</doi><tpages>6</tpages></addata></record> |
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subjects | Adult Associated diseases and complications Biological and medical sciences Blood Gas Monitoring, Transcutaneous Diabetes. Impaired glucose tolerance Diabetic Foot - diagnosis Diabetic Foot - physiopathology Diabetic Neuropathies - physiopathology Endocrine pancreas. Apud cells (diseases) Endocrinopathies Female Humans Male Medical sciences Middle Aged Perception Skin - physiopathology Vibration |
title | Hardness of Plantar Skin in Diabetic Neuropathic Feet |
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