Demographic, Health and Lifestyle Factors Associated with the Metabolome in Older Women

Author:

Navarro Sandi L.1ORCID,Nagana Gowda G. A.2ORCID,Bettcher Lisa F.2,Pepin Robert2,Nguyen Natalie2,Ellenberger Mathew2,Zheng Cheng3,Tinker Lesley F.1,Prentice Ross L.1,Huang Ying4,Yang Tao5ORCID,Tabung Fred K.6ORCID,Chan Queenie7ORCID,Loo Ruey Leng8ORCID,Liu Simin910ORCID,Wactawski-Wende Jean11ORCID,Lampe Johanna W.1,Neuhouser Marian L.1,Raftery Daniel12ORCID

Affiliation:

1. Cancer Prevention Program, Division of Public Health Sciences, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA

2. Department of Anesthesiology and Pain Medicine, University of Washington, Seattle, WA 98109, USA

3. Department of Biostatistics, University of Nebraska Medical Center, Omaha, NE 68198, USA

4. Biostatistics Program, Division of Public Health Sciences, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA

5. School of Public Health, Xinjiang Medical University, Urumqi 830011, China

6. Department of Internal Medicine, Division of Medical Oncology, College of Medicine and Comprehensive Cancer Center, The Ohio State University, Columbus, OH 43210, USA

7. School of Public Health, Imperial College of London, London SW7 2AZ, UK

8. Australian National Phenome Centre, Health Futures Institute, Murdoch University, Murdoch, WA 6150, Australia

9. Center for Global Cardiometabolic Health, Department of Epidemiology, School of Public Health, Providence, RI 02912, USA

10. Department of Medicine and Surgery, Alpert School of Medicine, Brown University, Providence, RI 02903, USA

11. Department of Epidemiology and Environmental Health, University at Buffalo, Buffalo, NY 14214, USA

Abstract

Demographic and clinical factors influence the metabolome. The discovery and validation of disease biomarkers are often challenged by potential confounding effects from such factors. To address this challenge, we investigated the magnitude of the correlation between serum and urine metabolites and demographic and clinical parameters in a well-characterized observational cohort of 444 post-menopausal women participating in the Women’s Health Initiative (WHI). Using LC-MS and lipidomics, we measured 157 aqueous metabolites and 756 lipid species across 13 lipid classes in serum, along with 195 metabolites detected by GC-MS and NMR in urine and evaluated their correlations with 29 potential disease risk factors, including demographic, dietary and lifestyle factors, and medication use. After controlling for multiple testing (FDR < 0.01), we found that log-transformed metabolites were mainly associated with age, BMI, alcohol intake, race, sample storage time (urine only), and dietary supplement use. Statistically significant correlations were in the absolute range of 0.2–0.6, with the majority falling below 0.4. Incorporation of important potential confounding factors in metabolite and disease association analyses may lead to improved statistical power as well as reduced false discovery rates in a variety of data analysis settings.

Funder

the National Heart, Lung, and Blood Institute, National Institutes of Health, U.S. Department of Health and Human Services

NCI

NIDDK

NIH

Publisher

MDPI AG

Subject

Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

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