| Literature DB >> 26810729 |
Richard L Doty1,2, Isabelle A Tourbier3,4, Dzung L Pham5, Jennifer L Cuzzocreo6, Jayaram K Udupa7, Bilge Karacali8, Evan Beals3,9, Laura Fabius3,4, Fidias E Leon-Sarmiento3,4, Gul Moonis10, Taehoon Kim3,4, Toru Mihama3,4, Rena J Geckle11, David M Yousem11.
Abstract
Empirical studies of taste function in multiple sclerosis (MS) are rare. Moreover, a detailed assessment of whether quantitative measures of taste function correlate with the punctate and patchy myelin-related lesions found throughout the CNS of MS patients has not been made. We administered a 96-trial test of sweet (sucrose), sour (citric acid), bitter (caffeine) and salty (NaCl) taste perception to the left and right anterior (CN VII) and posterior (CN IX) tongue regions of 73 MS patients and 73 matched controls. The number and volume of lesions were assessed using quantitative MRI in 52 brain regions of 63 of the MS patients. Taste identification scores were significantly lower in the MS patients for sucrose (p = 0.0002), citric acid (p = 0.0001), caffeine (p = 0.0372) and NaCl (p = 0.0004) and were present in both anterior and posterior tongue regions. The percent of MS patients with identification scores falling below the 5th percentile of controls was 15.07 % for caffeine, 21.9 % for citric acid, 24.66 % for sucrose, and 31.50 % for NaCl. Such scores were inversely correlated with lesion volumes in the temporal, medial frontal, and superior frontal lobes, and with the number of lesions in the left and right superior frontal lobes, right anterior cingulate gyrus, and left parietal operculum. Regardless of the subject group, women outperformed men on the taste measures. These findings indicate that a sizable number of MS patients exhibit taste deficits that are associated with MS-related lesions throughout the brain.Entities:
Keywords: Chemosensory transduction; Magnetic resonance imaging; Multiple sclerosis; Sex differences; Taste; Taste disorders
Mesh:
Year: 2016 PMID: 26810729 PMCID: PMC5399510 DOI: 10.1007/s00415-016-8030-6
Source DB: PubMed Journal: J Neurol ISSN: 0340-5354 Impact factor: 4.849