<_value> Cohort of Subjects Over 65 Years Old Consulting at Health Examination Centres for French Health Insurance EVATEM FRESH-PEF73139-en 73139 FRESH-PEF73139 Bruno FANTINO Christiane VANNIER-NITENBERG Bienvenu BONGUE Catherine SASS Olivier BEAUCHET Virginie DAUPHINOT Isabelle ROUCH Pierre KROLAK-SALMON CAISSE PRIMAIRE D ASSURANCE MALADIE DU RHONE (CPAM DU RHONE) Epidemiology France Portal (PEF) null Bruno;FANTINO Christiane;VANNIER-NITENBERG Bienvenu;BONGUE Catherine;SASS Olivier;BEAUCHET Virginie;DAUPHINOT Isabelle;ROUCH Pierre;KROLAK-SALMON CNIL memory loss slight cognitive deficiency balance Alzheimer’s early diagnosis Neurology Disorder of equilibrium Amnesia Socio-demographic and economic determinants Biological determinants: Genetic predisposition Healthcare system determinants: Access to care Biological determinants The main aim of the study is to assess the predictive values (PV) of three tests for diagnosing mild cognitive impairments, balance and disorders in elderly individuals who are alive. The secondary aim is the assess the relationship between falls and cognitive impairment. null France Auvergne Rhône-Alpes Pays de la Loire Individuals Patients population Male Female Aged (65 to 79 years) Aged, 80 and over (80 years and more) Subjects consulting at one of 3 health examination centres (Lyon, Angers and Saint-Etienne) for a free, periodic medical examination. 65 years old or over; living at home or in a non-medical institution. Volunteers participating in a periodic medical examination and presenting with a memory complaint (identified either by the patient or by a member of his/her family). Clinical data Paraclinical data (non-biological) Paraclinical data (non-biological) : Function testing Participant-reported health data Health event/morbidity Other Through organizations (health services or institutions schools businesses etc.) Medical-administrative database (patients health insurance/mutual insurance) [500-1000[ individuals Converting or copying information into a structured record Interview with the participant (including clinical) Observational Study Observational Study Cohort study 620 Unknown Restricted access Contact the principal investigator Access on specific project only