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Brain age prediction using deep learning uncovers associated sequence variants

Author

Listed:
  • B. A. Jonsson

    (deCODE Genetics/Amgen, Inc.
    University of Iceland)

  • G. Bjornsdottir

    (deCODE Genetics/Amgen, Inc.)

  • T. E. Thorgeirsson

    (deCODE Genetics/Amgen, Inc.)

  • L. M. Ellingsen

    (University of Iceland)

  • G. Bragi Walters

    (deCODE Genetics/Amgen, Inc.
    University of Iceland)

  • D. F. Gudbjartsson

    (deCODE Genetics/Amgen, Inc.
    University of Iceland)

  • H. Stefansson

    (deCODE Genetics/Amgen, Inc.)

  • K. Stefansson

    (deCODE Genetics/Amgen, Inc.
    University of Iceland)

  • M. O. Ulfarsson

    (deCODE Genetics/Amgen, Inc.
    University of Iceland)

Abstract

Machine learning algorithms can be trained to estimate age from brain structural MRI. The difference between an individual’s predicted and chronological age, predicted age difference (PAD), is a phenotype of relevance to aging and brain disease. Here, we present a new deep learning approach to predict brain age from a T1-weighted MRI. The method was trained on a dataset of healthy Icelanders and tested on two datasets, IXI and UK Biobank, utilizing transfer learning to improve accuracy on new sites. A genome-wide association study (GWAS) of PAD in the UK Biobank data (discovery set: $$N=12378$$N=12378, replication set: $$N=4456$$N=4456) yielded two sequence variants, rs1452628-T ($$\beta =-0.08$$β=−0.08, $$P=1.15\times{10}^{-9}$$P=1.15×10−9) and rs2435204-G ($$\beta =0.102$$β=0.102, $$P=9.73\times 1{0}^{-12}$$P=9.73×10−12). The former is near KCNK2 and correlates with reduced sulcal width, whereas the latter correlates with reduced white matter surface area and tags a well-known inversion at 17q21.31 (H2).

Suggested Citation

  • B. A. Jonsson & G. Bjornsdottir & T. E. Thorgeirsson & L. M. Ellingsen & G. Bragi Walters & D. F. Gudbjartsson & H. Stefansson & K. Stefansson & M. O. Ulfarsson, 2019. "Brain age prediction using deep learning uncovers associated sequence variants," Nature Communications, Nature, vol. 10(1), pages 1-10, December.
  • Handle: RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-13163-9
    DOI: 10.1038/s41467-019-13163-9
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    Cited by:

    1. Seungmin Lee & Jeong Soo Park & Hyowon Woo & Yong Kyoung Yoo & Dongho Lee & Seok Chung & Dae Sung Yoon & Ki- Baek Lee & Jeong Hoon Lee, 2024. "Rapid deep learning-assisted predictive diagnostics for point-of-care testing," Nature Communications, Nature, vol. 15(1), pages 1-12, December.
    2. Mit Shah & Marco H. A. Inácio & Chang Lu & Pierre-Raphaël Schiratti & Sean L. Zheng & Adam Clement & Antonio Marvao & Wenjia Bai & Andrew P. King & James S. Ware & Martin R. Wilkins & Johanna Mielke &, 2023. "Environmental and genetic predictors of human cardiovascular ageing," Nature Communications, Nature, vol. 14(1), pages 1-15, December.
    3. Benjamin B. Sun & Stephanie J. Loomis & Fabrizio Pizzagalli & Natalia Shatokhina & Jodie N. Painter & Christopher N. Foley & Megan E. Jensen & Donald G. McLaren & Sai Spandana Chintapalli & Alyssa H. , 2022. "Genetic map of regional sulcal morphology in the human brain from UK biobank data," Nature Communications, Nature, vol. 13(1), pages 1-13, December.
    4. Junhao Wen & Bingxin Zhao & Zhijian Yang & Guray Erus & Ioanna Skampardoni & Elizabeth Mamourian & Yuhan Cui & Gyujoon Hwang & Jingxuan Bao & Aleix Boquet-Pujadas & Zhen Zhou & Yogasudha Veturi & Mary, 2024. "The genetic architecture of multimodal human brain age," Nature Communications, Nature, vol. 15(1), pages 1-15, December.
    5. Jordi Manuello & Joosung Min & Paul McCarthy & Fidel Alfaro-Almagro & Soojin Lee & Stephen Smith & Lloyd T. Elliott & Anderson M. Winkler & Gwenaëlle Douaud, 2024. "The effects of genetic and modifiable risk factors on brain regions vulnerable to ageing and disease," Nature Communications, Nature, vol. 15(1), pages 1-11, December.

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