Genetic Architecture of Plasma Alpha-Aminoadipic Acid Reveals a Relationship With High-Density Lipoprotein Cholesterol

Research output: Contribution to journalJournal articleResearchpeer-review

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Genetic Architecture of Plasma Alpha-Aminoadipic Acid Reveals a Relationship With High-Density Lipoprotein Cholesterol. / Shi, Mingjian; Wang, C; Mei, H; Temprosa, Marinella; Florez, JC; Tripputi, M; Merino, Jordi; Lipworth, L; Shu, XO; Gerszten, Robert; Wang, Thomas; Beckman, Joshua; Gamboa, Jorge; Mosley, Jonathan D.; Ferguson, Jane; Group, Diabetes Prevention Program Research.

In: Journal of the American Heart Association, Vol. 11, No. 11, 2022.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Shi, M, Wang, C, Mei, H, Temprosa, M, Florez, JC, Tripputi, M, Merino, J, Lipworth, L, Shu, XO, Gerszten, R, Wang, T, Beckman, J, Gamboa, J, Mosley, JD, Ferguson, J & Group, DPPR 2022, 'Genetic Architecture of Plasma Alpha-Aminoadipic Acid Reveals a Relationship With High-Density Lipoprotein Cholesterol', Journal of the American Heart Association, vol. 11, no. 11. https://doi.org/10.1161/jaha.121.024388

APA

Shi, M., Wang, C., Mei, H., Temprosa, M., Florez, JC., Tripputi, M., Merino, J., Lipworth, L., Shu, XO., Gerszten, R., Wang, T., Beckman, J., Gamboa, J., Mosley, J. D., Ferguson, J., & Group, D. P. P. R. (2022). Genetic Architecture of Plasma Alpha-Aminoadipic Acid Reveals a Relationship With High-Density Lipoprotein Cholesterol. Journal of the American Heart Association, 11(11). https://doi.org/10.1161/jaha.121.024388

Vancouver

Shi M, Wang C, Mei H, Temprosa M, Florez JC, Tripputi M et al. Genetic Architecture of Plasma Alpha-Aminoadipic Acid Reveals a Relationship With High-Density Lipoprotein Cholesterol. Journal of the American Heart Association. 2022;11(11). https://doi.org/10.1161/jaha.121.024388

Author

Shi, Mingjian ; Wang, C ; Mei, H ; Temprosa, Marinella ; Florez, JC ; Tripputi, M ; Merino, Jordi ; Lipworth, L ; Shu, XO ; Gerszten, Robert ; Wang, Thomas ; Beckman, Joshua ; Gamboa, Jorge ; Mosley, Jonathan D. ; Ferguson, Jane ; Group, Diabetes Prevention Program Research. / Genetic Architecture of Plasma Alpha-Aminoadipic Acid Reveals a Relationship With High-Density Lipoprotein Cholesterol. In: Journal of the American Heart Association. 2022 ; Vol. 11, No. 11.

Bibtex

@article{679071bc35bf46109a43c9f304e2f922,
title = "Genetic Architecture of Plasma Alpha-Aminoadipic Acid Reveals a Relationship With High-Density Lipoprotein Cholesterol",
abstract = "Background Elevated plasma levels of alpha-aminoadipic acid (2-AAA) have been associated with the development of type 2 diabetes and atherosclerosis. However, the nature of the association remains unknown. Methods and Results We identified genetic determinants of plasma 2-AAA through meta-analysis of genome-wide association study data in 5456 individuals of European, African, and Asian ancestry from the Framingham Heart Study, Diabetes Prevention Program, Jackson Heart Study, and Shanghai Women's and Men's Health Studies. No single nucleotide polymorphisms reached genome-wide significance across all samples. However, the top associations from the meta-analysis included single-nucleotide polymorphisms in the known 2-AAA pathway gene DHTKD1, and single-nucleotide polymorphisms in genes involved in mitochondrial respiration (NDUFS4) and macrophage function (MSR1). We used a Mendelian randomization instrumental variable approach to evaluate relationships between 2-AAA and cardiometabolic phenotypes in large disease genome-wide association studies. Mendelian randomization identified a suggestive inverse association between increased 2-AAA and lower high-density lipoprotein cholesterol (P=0.005). We further characterized the genetically predicted relationship through measurement of plasma 2-AAA and high-density lipoprotein cholesterol in 2 separate samples of individuals with and without cardiometabolic disease (N=98), and confirmed a significant negative correlation between 2-AAA and high-density lipoprotein (rs=-0.53, P",
author = "Mingjian Shi and C Wang and H Mei and Marinella Temprosa and JC Florez and M Tripputi and Jordi Merino and L Lipworth and XO Shu and Robert Gerszten and Thomas Wang and Joshua Beckman and Jorge Gamboa and Mosley, {Jonathan D.} and Jane Ferguson and Group, {Diabetes Prevention Program Research}",
year = "2022",
doi = "10.1161/jaha.121.024388",
language = "English",
volume = "11",
journal = "Journal of the American Heart Association",
issn = "2047-9980",
publisher = "Wiley-Blackwell",
number = "11",

}

RIS

TY - JOUR

T1 - Genetic Architecture of Plasma Alpha-Aminoadipic Acid Reveals a Relationship With High-Density Lipoprotein Cholesterol

AU - Shi, Mingjian

AU - Wang, C

AU - Mei, H

AU - Temprosa, Marinella

AU - Florez, JC

AU - Tripputi, M

AU - Merino, Jordi

AU - Lipworth, L

AU - Shu, XO

AU - Gerszten, Robert

AU - Wang, Thomas

AU - Beckman, Joshua

AU - Gamboa, Jorge

AU - Mosley, Jonathan D.

AU - Ferguson, Jane

AU - Group, Diabetes Prevention Program Research

PY - 2022

Y1 - 2022

N2 - Background Elevated plasma levels of alpha-aminoadipic acid (2-AAA) have been associated with the development of type 2 diabetes and atherosclerosis. However, the nature of the association remains unknown. Methods and Results We identified genetic determinants of plasma 2-AAA through meta-analysis of genome-wide association study data in 5456 individuals of European, African, and Asian ancestry from the Framingham Heart Study, Diabetes Prevention Program, Jackson Heart Study, and Shanghai Women's and Men's Health Studies. No single nucleotide polymorphisms reached genome-wide significance across all samples. However, the top associations from the meta-analysis included single-nucleotide polymorphisms in the known 2-AAA pathway gene DHTKD1, and single-nucleotide polymorphisms in genes involved in mitochondrial respiration (NDUFS4) and macrophage function (MSR1). We used a Mendelian randomization instrumental variable approach to evaluate relationships between 2-AAA and cardiometabolic phenotypes in large disease genome-wide association studies. Mendelian randomization identified a suggestive inverse association between increased 2-AAA and lower high-density lipoprotein cholesterol (P=0.005). We further characterized the genetically predicted relationship through measurement of plasma 2-AAA and high-density lipoprotein cholesterol in 2 separate samples of individuals with and without cardiometabolic disease (N=98), and confirmed a significant negative correlation between 2-AAA and high-density lipoprotein (rs=-0.53, P

AB - Background Elevated plasma levels of alpha-aminoadipic acid (2-AAA) have been associated with the development of type 2 diabetes and atherosclerosis. However, the nature of the association remains unknown. Methods and Results We identified genetic determinants of plasma 2-AAA through meta-analysis of genome-wide association study data in 5456 individuals of European, African, and Asian ancestry from the Framingham Heart Study, Diabetes Prevention Program, Jackson Heart Study, and Shanghai Women's and Men's Health Studies. No single nucleotide polymorphisms reached genome-wide significance across all samples. However, the top associations from the meta-analysis included single-nucleotide polymorphisms in the known 2-AAA pathway gene DHTKD1, and single-nucleotide polymorphisms in genes involved in mitochondrial respiration (NDUFS4) and macrophage function (MSR1). We used a Mendelian randomization instrumental variable approach to evaluate relationships between 2-AAA and cardiometabolic phenotypes in large disease genome-wide association studies. Mendelian randomization identified a suggestive inverse association between increased 2-AAA and lower high-density lipoprotein cholesterol (P=0.005). We further characterized the genetically predicted relationship through measurement of plasma 2-AAA and high-density lipoprotein cholesterol in 2 separate samples of individuals with and without cardiometabolic disease (N=98), and confirmed a significant negative correlation between 2-AAA and high-density lipoprotein (rs=-0.53, P

U2 - 10.1161/jaha.121.024388

DO - 10.1161/jaha.121.024388

M3 - Journal article

C2 - 35621206

VL - 11

JO - Journal of the American Heart Association

JF - Journal of the American Heart Association

SN - 2047-9980

IS - 11

ER -

ID: 347793226