Multiple determinants of lifespan memory differences

نویسندگان

  • Richard N. Henson
  • Karen L. Campbell
  • Simon W. Davis
  • Jason R. Taylor
  • Tina Emery
  • Sharon Erzinclioglu
  • Lorraine K. Tyler
  • Carol Brayne
  • Edward T. Bullmore
  • Andrew C. Calder
  • Rhodri Cusack
  • Tim Dalgleish
  • John Duncan
  • Fiona E. Matthews
  • William D. Marslen-Wilson
  • James B. Rowe
  • Meredith A. Shafto
  • Teresa Cheung
  • Linda Geerligs
  • Anna McCarrey
  • Abdur Mustafa
  • Darren Price
  • David Samu
  • Matthias Treder
  • Kamen A. Tsvetanov
  • Janna van Belle
  • Nitin Williams
  • Lauren Bates
  • Andrew Gadie
  • Sofia Gerbase
  • Stanimira Georgieva
  • Claire Hanley
  • Beth Parkin
  • David Troy
  • Tibor Auer
  • Marta Correia
  • Lu Gao
  • Emma Green
  • Rafael Henriques
  • Jodie Allen
  • Gillian Amery
  • Liana Amunts
  • Anne Barcroft
  • Amanda Castle
  • Cheryl Dias
  • Jonathan Dowrick
  • Melissa Fair
  • Hayley Fisher
  • Anna Goulding
  • Adarsh Grewa
  • Geoff Hale
  • Andrew Hilton
  • Frances Johnson
  • Patricia Johnston
  • Thea Kavanagh-Williamson
  • Magdalena Kwasniewska
  • Alison McMinn
  • Kim Norman
  • Jessica Penrose
  • Fiona Roby
  • Diane Rowland
  • John Sargeant
  • Maggie Squire
  • Beth Stevens
  • Aldabra Stoddart
  • Cheryl Stone
  • Tracy Thompson
  • Ozlem Yazlik
  • Dan Barnes
  • Marie Dixon
  • Jaya Hillman
  • Joanne Mitchell
  • Laura Villis
  • Rogier A. Kievit
چکیده

Memory problems are among the most common complaints as people grow older. Using structural equation modeling of commensurate scores of anterograde memory from a large (N = 315), population-derived sample (www.cam-can.org), we provide evidence for three memory factors that are supported by distinct brain regions and show differential sensitivity to age. Associative memory and item memory are dramatically affected by age, even after adjusting for education level and fluid intelligence, whereas visual priming is not. Associative memory and item memory are differentially affected by emotional valence, and the age-related decline in associative memory is faster for negative than for positive or neutral stimuli. Gray-matter volume in the hippocampus, parahippocampus and fusiform cortex, and a white-matter index for the fornix, uncinate fasciculus and inferior longitudinal fasciculus, show differential contributions to the three memory factors. Together, these data demonstrate the extent to which differential ageing of the brain leads to differential patterns of memory loss.

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عنوان ژورنال:

دوره 6  شماره 

صفحات  -

تاریخ انتشار 2016