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.Základní údaje
Originální název
Sensory phenotype and risk factors for painful diabetic neuropathy: a cross-sectional observational study
Autoři
RAPUTOVÁ, Jana; Iva ŠROTOVÁ; Eva VLČKOVÁ; Claudia SOMMER; Nurcan ÜCEYLER; Frank BIRKLEIN; Heike L. RITTNER; Cora REBHORN; Blanka ADAMOVÁ; Ivana KOVAĽOVÁ; Eva KRÁLÍČKOVÁ NEKVAPILOVÁ; Lucas FORER; Jana BĚLOBRÁDKOVÁ; Jindřich OLŠOVSKÝ; Pavel WEBER; Ladislav DUŠEK; Jiří JARKOVSKÝ ORCID a Josef BEDNAŘÍK
Vydání
Pain, Philadelphia, Lippincott Williams & Wilkins, 2017, 0304-3959
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30103 Neurosciences
Stát vydavatele
Spojené státy
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 5.559
Kód RIV
RIV/00216224:14110/17:00098445
Organizační jednotka
Lékařská fakulta
UT WoS
000419133700009
EID Scopus
2-s2.0-85036546328
Klíčová slova anglicky
diabetic neuropathy
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 13. 3. 2018 13:39, Soňa Böhmová
Anotace
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.