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Bile acids targeted metabolomics and medication classification data in the ADNI1 and ADNIGO/2 cohorts.

Publication ,  Journal Article
St John-Williams, L; Mahmoudiandehkordi, S; Arnold, M; Massaro, T; Blach, C; Kastenmüller, G; Louie, G; Kueider-Paisley, A; Han, X; Baillie, R ...
Published in: Sci Data
October 17, 2019

Alzheimer's disease (AD) is the most common cause of dementia. The mechanism of disease development and progression is not well understood, but increasing evidence suggests multifactorial etiology, with a number of genetic, environmental, and aging-related factors. There is a growing body of evidence that metabolic defects may contribute to this complex disease. To interrogate the relationship between system level metabolites and disease susceptibility and progression, the AD Metabolomics Consortium (ADMC) in partnership with AD Neuroimaging Initiative (ADNI) is creating a comprehensive biochemical database for patients in the ADNI1 cohort. We used the Biocrates Bile Acids platform to evaluate the association of metabolic levels with disease risk and progression. We detail the quantitative metabolomics data generated on the baseline samples from ADNI1 and ADNIGO/2 (370 cognitively normal, 887 mild cognitive impairment, and 305 AD). Similar to our previous reports on ADNI1, we present the tools for data quality control and initial analysis. This data descriptor represents the third in a series of comprehensive metabolomics datasets from the ADMC on the ADNI.

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Published In

Sci Data

DOI

EISSN

2052-4463

Publication Date

October 17, 2019

Volume

6

Issue

1

Start / End Page

212

Location

England

Related Subject Headings

  • Metabolomics
  • Male
  • Humans
  • Female
  • Disease Progression
  • Bile Acids and Salts
  • Alzheimer Disease
  • Aged, 80 and over
  • Aged
 

Citation

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St John-Williams, L., Mahmoudiandehkordi, S., Arnold, M., Massaro, T., Blach, C., Kastenmüller, G., … Alzheimer’s Disease Metabolomics Consortium, . (2019). Bile acids targeted metabolomics and medication classification data in the ADNI1 and ADNIGO/2 cohorts. Sci Data, 6(1), 212. https://doi.org/10.1038/s41597-019-0181-8
St John-Williams, Lisa, Siamak Mahmoudiandehkordi, Matthias Arnold, Tyler Massaro, Colette Blach, Gabi Kastenmüller, Gregory Louie, et al. “Bile acids targeted metabolomics and medication classification data in the ADNI1 and ADNIGO/2 cohorts.Sci Data 6, no. 1 (October 17, 2019): 212. https://doi.org/10.1038/s41597-019-0181-8.
St John-Williams L, Mahmoudiandehkordi S, Arnold M, Massaro T, Blach C, Kastenmüller G, et al. Bile acids targeted metabolomics and medication classification data in the ADNI1 and ADNIGO/2 cohorts. Sci Data. 2019 Oct 17;6(1):212.
St John-Williams, Lisa, et al. “Bile acids targeted metabolomics and medication classification data in the ADNI1 and ADNIGO/2 cohorts.Sci Data, vol. 6, no. 1, Oct. 2019, p. 212. Pubmed, doi:10.1038/s41597-019-0181-8.
St John-Williams L, Mahmoudiandehkordi S, Arnold M, Massaro T, Blach C, Kastenmüller G, Louie G, Kueider-Paisley A, Han X, Baillie R, Motsinger-Reif AA, Rotroff D, Nho K, Saykin AJ, Risacher SL, Koal T, Moseley MA, Tenenbaum JD, Thompson JW, Kaddurah-Daouk R, Alzheimer’s Disease Neuroimaging Initiative, Alzheimer’s Disease Metabolomics Consortium. Bile acids targeted metabolomics and medication classification data in the ADNI1 and ADNIGO/2 cohorts. Sci Data. 2019 Oct 17;6(1):212.

Published In

Sci Data

DOI

EISSN

2052-4463

Publication Date

October 17, 2019

Volume

6

Issue

1

Start / End Page

212

Location

England

Related Subject Headings

  • Metabolomics
  • Male
  • Humans
  • Female
  • Disease Progression
  • Bile Acids and Salts
  • Alzheimer Disease
  • Aged, 80 and over
  • Aged