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Truncal Pruritus of Unknown Origin May Be a Symptom of Diabetic Polyneuropathy

OBJECTIVE: Our goal was to ascertain the prevalence of pruritus in diabetic and nondiabetic subjects and the relevance of symptoms, signs, and nerve functions of diabetic polyneuropathy (DPN) of pruritus. RESEARCH DESIGN AND METHODS: A large-scale survey of 2,656 diabetic outpatients and 499 nondiab...

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Autores principales: Yamaoka, Hiroyuki, Sasaki, Hideyuki, Yamasaki, Hiroshi, Ogawa, Kenichi, Ohta, Takayuki, Furuta, Hiroto, Nishi, Masahiro, Nanjo, Kishio
Formato: Texto
Lenguaje:English
Publicado: American Diabetes Association 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2797961/
https://www.ncbi.nlm.nih.gov/pubmed/20040674
http://dx.doi.org/10.2337/dc09-0632
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author Yamaoka, Hiroyuki
Sasaki, Hideyuki
Yamasaki, Hiroshi
Ogawa, Kenichi
Ohta, Takayuki
Furuta, Hiroto
Nishi, Masahiro
Nanjo, Kishio
author_facet Yamaoka, Hiroyuki
Sasaki, Hideyuki
Yamasaki, Hiroshi
Ogawa, Kenichi
Ohta, Takayuki
Furuta, Hiroto
Nishi, Masahiro
Nanjo, Kishio
author_sort Yamaoka, Hiroyuki
collection PubMed
description OBJECTIVE: Our goal was to ascertain the prevalence of pruritus in diabetic and nondiabetic subjects and the relevance of symptoms, signs, and nerve functions of diabetic polyneuropathy (DPN) of pruritus. RESEARCH DESIGN AND METHODS: A large-scale survey of 2,656 diabetic outpatients and 499 nondiabetic subjects was performed. In diabetic subjects, the relationship between pruritus and age, sex, diabetic duration, A1C, Achilles tendon reflex (ATR), and abnormal sensation in legs was evaluated. In 105 diabetic subjects, nerve conduction studies, quantitative vibratory threshold (QVT), heart rate variability, and a fall of systolic blood pressure at a head-up tilt test (ΔBP) were performed, and the relationships between pruritus and nerve functions were evaluated. RESULTS: Although the prevalence of truncal pruritus of unknown origin (TPUO) in diabetic subjects was significantly higher than that in age-matched nondiabetic subjects (11.3 vs. 2.9%, P = 0.0001), the prevalence of other pruritus was not different between the two groups. Multiple logistic regression analysis revealed that abnormal sensation and ATR areflexia were independent risk factors for TPUO in age, sex, duration of diabetes, and A1C. ΔBP in diabetic subjects with TPUO was significantly impaired compared with that in those without TPUO. Larger ΔBP was identified as a significant risk factor of TPUO independent of other nerve dysfunctions by multiple logistic regression analysis. CONCLUSIONS: TPUO is significantly more frequent in diabetic than in nondiabetic individuals. TPUO is significantly associated with symptoms and signs of DPN, including impaired blood pressure response in a head-up tilt test. TPUO, therefore, might be a newly recognized symptom of DPN.
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spelling pubmed-27979612011-01-01 Truncal Pruritus of Unknown Origin May Be a Symptom of Diabetic Polyneuropathy Yamaoka, Hiroyuki Sasaki, Hideyuki Yamasaki, Hiroshi Ogawa, Kenichi Ohta, Takayuki Furuta, Hiroto Nishi, Masahiro Nanjo, Kishio Diabetes Care Original Research OBJECTIVE: Our goal was to ascertain the prevalence of pruritus in diabetic and nondiabetic subjects and the relevance of symptoms, signs, and nerve functions of diabetic polyneuropathy (DPN) of pruritus. RESEARCH DESIGN AND METHODS: A large-scale survey of 2,656 diabetic outpatients and 499 nondiabetic subjects was performed. In diabetic subjects, the relationship between pruritus and age, sex, diabetic duration, A1C, Achilles tendon reflex (ATR), and abnormal sensation in legs was evaluated. In 105 diabetic subjects, nerve conduction studies, quantitative vibratory threshold (QVT), heart rate variability, and a fall of systolic blood pressure at a head-up tilt test (ΔBP) were performed, and the relationships between pruritus and nerve functions were evaluated. RESULTS: Although the prevalence of truncal pruritus of unknown origin (TPUO) in diabetic subjects was significantly higher than that in age-matched nondiabetic subjects (11.3 vs. 2.9%, P = 0.0001), the prevalence of other pruritus was not different between the two groups. Multiple logistic regression analysis revealed that abnormal sensation and ATR areflexia were independent risk factors for TPUO in age, sex, duration of diabetes, and A1C. ΔBP in diabetic subjects with TPUO was significantly impaired compared with that in those without TPUO. Larger ΔBP was identified as a significant risk factor of TPUO independent of other nerve dysfunctions by multiple logistic regression analysis. CONCLUSIONS: TPUO is significantly more frequent in diabetic than in nondiabetic individuals. TPUO is significantly associated with symptoms and signs of DPN, including impaired blood pressure response in a head-up tilt test. TPUO, therefore, might be a newly recognized symptom of DPN. American Diabetes Association 2010-01 /pmc/articles/PMC2797961/ /pubmed/20040674 http://dx.doi.org/10.2337/dc09-0632 Text en © 2010 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details.
spellingShingle Original Research
Yamaoka, Hiroyuki
Sasaki, Hideyuki
Yamasaki, Hiroshi
Ogawa, Kenichi
Ohta, Takayuki
Furuta, Hiroto
Nishi, Masahiro
Nanjo, Kishio
Truncal Pruritus of Unknown Origin May Be a Symptom of Diabetic Polyneuropathy
title Truncal Pruritus of Unknown Origin May Be a Symptom of Diabetic Polyneuropathy
title_full Truncal Pruritus of Unknown Origin May Be a Symptom of Diabetic Polyneuropathy
title_fullStr Truncal Pruritus of Unknown Origin May Be a Symptom of Diabetic Polyneuropathy
title_full_unstemmed Truncal Pruritus of Unknown Origin May Be a Symptom of Diabetic Polyneuropathy
title_short Truncal Pruritus of Unknown Origin May Be a Symptom of Diabetic Polyneuropathy
title_sort truncal pruritus of unknown origin may be a symptom of diabetic polyneuropathy
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2797961/
https://www.ncbi.nlm.nih.gov/pubmed/20040674
http://dx.doi.org/10.2337/dc09-0632
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