Detailed Information on Publication Record
2017
Sensory phenotype and risk factors for painful diabetic neuropathy: a cross-sectional observational study
RAPUTOVÁ, Jana, Iva ŠROTOVÁ, Eva VLČKOVÁ, Claudia SOMMER, Nurcan ÜCEYLER et. al.Basic information
Original name
Sensory phenotype and risk factors for painful diabetic neuropathy: a cross-sectional observational study
Authors
RAPUTOVÁ, Jana (203 Czech Republic, belonging to the institution), Iva ŠROTOVÁ (203 Czech Republic, belonging to the institution), Eva VLČKOVÁ (203 Czech Republic, belonging to the institution), Claudia SOMMER (276 Germany), Nurcan ÜCEYLER (276 Germany), Frank BIRKLEIN (276 Germany), Heike L. RITTNER (276 Germany), Cora REBHORN (276 Germany), Blanka ADAMOVÁ (203 Czech Republic, belonging to the institution), Ivana KOVAĽOVÁ (703 Slovakia, belonging to the institution), Eva KRÁLÍČKOVÁ NEKVAPILOVÁ (203 Czech Republic), Lucas FORER (40 Austria), Jana BĚLOBRÁDKOVÁ (203 Czech Republic), Jindřich OLŠOVSKÝ (203 Czech Republic), Pavel WEBER (203 Czech Republic), Ladislav DUŠEK (203 Czech Republic, belonging to the institution), Jiří JARKOVSKÝ (203 Czech Republic, belonging to the institution) and Josef BEDNAŘÍK (203 Czech Republic, guarantor, belonging to the institution)
Edition
Pain, Philadelphia, Lippincott Williams & Wilkins, 2017, 0304-3959
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30103 Neurosciences
Country of publisher
United States of America
Confidentiality degree
není předmětem státního či obchodního tajemství
Impact factor
Impact factor: 5.559
RIV identification code
RIV/00216224:14110/17:00098445
Organization unit
Faculty of Medicine
UT WoS
000419133700009
Keywords in English
diabetic neuropathy
Tags
International impact, Reviewed
Změněno: 13/3/2018 13:39, Soňa Böhmová
Abstract
V originále
Different sensory profiles in diabetic distal symmetrical sensory-motor polyneuropathy (DSPN) may be associated with pain and the responsiveness to analgesia. We aimed to characterize sensory phenotypes of patients with painful and painless diabetic neuropathy and to assess demographic, clinical, metabolic, and electrophysiological parameters related to the presence of neuropathic pain in a large cohort of well-defined DSPN subjects. This observational cross-sectional multi-center cohort study (performed as part of the ncRNAPain EU consortium) of 232 subjects with nonpainful (n = 74) and painful (n = 158) DSPN associated with diabetes mellitus of type 1 and 2 (median age 63 years, range 21-87 years; 92 women) comprised detailed history taking, laboratory tests, neurological examination, quantitative sensory testing, nerve conduction studies, and neuropathy severity scores. All parameters were analyzed with regard to the presence and severity of neuropathic pain. Neuropathic pain was positively correlated with the severity of neuropathy and thermal hyposensitivity (P < 0.001). A minority of patients with painful DSPN (14.6%) had a sensory profile, indicating thermal hypersensitivity that was associated with less severe neuropathy. Neuropathic pain was further linked to female sex and higher cognitive appraisal of pain as assessed by the pain catastrophizing scale (P < 0.001), while parameters related to diabetes showed no influence on neuropathic pain with the exception of laboratory signs of nephropathy. This study confirms the value of comprehensive DSPN phenotyping and underlines the importance of the severity of neuropathy for the presence of pain. Different sensory phenotypes might be useful for stratification of patients with painful DSPN for analgesic treatment and drug trials.