PMID- 25749905 OWN - NLM STAT- MEDLINE DCOM- 20160427 LR - 20181202 IS - 1720-8319 (Electronic) IS - 1594-0667 (Linking) VI - 27 IP - 5 DP - 2015 Oct TI - Evaluation of the cholinergic hypothesis in Alzheimer's disease with neuropsychological methods. PG - 727-33 LID - 10.1007/s40520-015-0321-8 [doi] AB - AIM: This study aimed at evaluating the cholinergic hypothesis in Alzheimer's disease (AD) patients utilizing the pupillometry method, cognitive tests and Hamilton Depression Rating Scale (HAM-D), as well as to examine whether a correlation between cognitive tests and pupillometry exists. METHODS: Forty-two patients with mean age 69.2 +/- 7.0 years and documented AD volunteered to participate in this study, while 33 healthy matched subjects served as controls. All subjects underwent a pupillometric measurement and performed the Wechsler Memory Scale (WMS) and Mini Mental State Examination (MMSE). Also, HAM-D was used to assess the severity of depressive symptoms. The pupillometric parameters studied were (1) latency for the onset of constriction (T1), (2) maximum constriction velocity (VCmax), and (3) maximum constriction acceleration (ACmax). RESULTS: In AD patients MMSE and WMS score were correlated with ACmax (r = -0.409, p < 0.05 and r = -0.513, p < 0.05, respectively) and VCmax (r = -0.664, p < 0.05 and r = -0.771, p < 0.05), respectively. Moreover, T1 was found to be significantly increased by 23 % (p < 0.05) in AD patients compared to healthy subjects. Conversely, the mean scores of VCmax and ACmax were significantly decreased in AD patients by 46 % (p < 0.05) and by 47 % (p < 0.05), respectively, as compared to healthy subjects. There was no significant difference between the two groups for HAM-D. Additionally, AD patients showed decreased score in WMS by 40 % (p < 0.05) and in MMSE by 28.5 % (p < 0.05) compared to healthy subjects. Of the indices that were studied VCmax and ACmax are governed mainly by the action of the Parasympathetic Nervous System. CONCLUSIONS: The results of this study demonstrated that there is a correlation between cognitive tests and pupillometry in AD patients. Thus, pupillometry could be considered as a sensitive technique for the investigation of cholinergic deficits, which indirectly lead to memory and cognitive disorders in AD patients. FAU - Fotiou, Dimitrios AU - Fotiou D AD - Neuroscience Division, Medicine School, A Neurology Clinic of AHEPA Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece. FAU - Kaltsatou, Antonia AU - Kaltsatou A AD - Neuroscience Division, Medicine School, A Neurology Clinic of AHEPA Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece. akaltsat@phed.auth.gr. AD - Department of Physical Education and Sport Science, University of Thessaly, Karies, 42100, Trikala, Greece. akaltsat@phed.auth.gr. FAU - Tsiptsios, Dimitrios AU - Tsiptsios D AD - Neuroscience Division, Medicine School, A Neurology Clinic of AHEPA Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece. FAU - Nakou, Maria AU - Nakou M AD - Neuroscience Division, Medicine School, A Neurology Clinic of AHEPA Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece. LA - eng PT - Journal Article DEP - 20150308 PL - Germany TA - Aging Clin Exp Res JT - Aging clinical and experimental research JID - 101132995 RN - 0 (Cholinergic Agents) RN - N9YNS0M02X (Acetylcholine) RN - X4W3ENH1CV (Norepinephrine) SB - IM MH - Acetylcholine/metabolism MH - Aged MH - *Alzheimer Disease/diagnosis/metabolism/psychology MH - Cholinergic Agents MH - Cognition/physiology MH - *Cognition Disorders/etiology/metabolism MH - Depression/*diagnosis MH - Female MH - Humans MH - Intelligence Tests MH - Male MH - Memory/physiology MH - Middle Aged MH - Neuropsychological Tests MH - Norepinephrine/metabolism MH - *Reflex, Pupillary MH - Statistics as Topic MH - Synaptic Transmission/*physiology OTO - NOTNLM OT - Alzheimer's disease OT - Cholinergic hypothesis OT - Cognitive function OT - Neuropsychological methods OT - Pupillometry EDAT- 2015/03/10 06:00 MHDA- 2016/04/28 06:00 CRDT- 2015/03/10 06:00 PHST- 2015/01/12 00:00 [received] PHST- 2015/01/20 00:00 [accepted] PHST- 2015/03/10 06:00 [entrez] PHST- 2015/03/10 06:00 [pubmed] PHST- 2016/04/28 06:00 [medline] AID - 10.1007/s40520-015-0321-8 [pii] AID - 10.1007/s40520-015-0321-8 [doi] PST - ppublish SO - Aging Clin Exp Res. 2015 Oct;27(5):727-33. doi: 10.1007/s40520-015-0321-8. Epub 2015 Mar 8.