A catalog of genetic loci associated with kidney function from analyses of a million individuals
書誌事項
- 公開日
- 2019-05-31
- 権利情報
-
- http://www.springer.com/tdm
- http://www.springer.com/tdm
- DOI
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- 10.1038/s41588-019-0407-x
- 10.17863/cam.39829
- 10.5167/uzh-176744
- 10.7892/boris.131296
- 公開者
- Springer Science and Business Media LLC
この論文をさがす
説明
Chronic kidney disease (CKD) is responsible for a public health burden with multi-systemic complications. Through trans-ancestry meta-analysis of genome-wide association studies of estimated glomerular filtration rate (eGFR) and independent replication (n = 1,046,070), we identified 264 associated loci (166 new). Of these, 147 were likely to be relevant for kidney function on the basis of associations with the alternative kidney function marker blood urea nitrogen (n = 416,178). Pathway and enrichment analyses, including mouse models with renal phenotypes, support the kidney as the main target organ. A genetic risk score for lower eGFR was associated with clinically diagnosed CKD in 452,264 independent individuals. Colocalization analyses of associations with eGFR among 783,978 European-ancestry individuals and gene expression across 46 human tissues, including tubulo-interstitial and glomerular kidney compartments, identified 17 genes differentially expressed in kidney. Fine-mapping highlighted missense driver variants in 11 genes and kidney-specific regulatory variants. These results provide a comprehensive priority list of molecular targets for translational research.
収録刊行物
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- Nature Genetics
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Nature Genetics 51 (6), 957-972, 2019-05-31
Springer Science and Business Media LLC
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キーワード
- EMC MM-04-54-08-A
- catalog
- ddc:000
- Inheritance Patterns
- Hasso-Plattner-Institut für Digital Engineering GmbH
- Kidney Function Tests
- DISEASE
- 10052 Institute of Physiology
- Uromodulin/urine
- Disease
- Renal Insufficiency
- kidney function
- 11 Medical and Health Sciences
- Genetics & Heredity
- Genome-wide association
- HERITABILITY
- GENOME-WIDE ASSOCIATION ; COMMON VARIANTS ; RENAL-FUNCTION ; TRANS-EQTLS ; DISEASE ; METAANALYSIS ; TRANSPORTER ; CLASSIFICATION ; HERITABILITY ; INTEGRATION
- Nierenfunktion
- COMMON VARIANTS
- Chromosome Mapping
- Single Nucleotide
- [SDV] Life Sciences [q-bio]
- Phenotype
- Genome-wide association; Common variants; Renal function; Trans-EQTLS; Disease; Metaanalysis; Heritability; Transporter
- Life Sciences & Biomedicine
- INTEGRATION
- Glomerular Filtration Rate
- Metaanalysi
- RENAL-FUNCTION
- /dk/atira/pure/subjectarea/asjc/1300/1311
- name=Genetics
- European Continental Ancestry Group
- Quantitative Trait Loci
- 610
- 610 Medicine & health
- Common variant
- Trans-EQTLS
- Transporter
- Polymorphism, Single Nucleotide
- V. A. Million Veteran Program
- CLASSIFICATION
- White People
- Chronic/genetics
- Heritability
- Quantitative Trait
- Quantitative Trait, Heritable
- 1311 Genetics
- Lifelines Cohort Study
- 616
- Uromodulin
- Genetics
- Humans
- Genetic Predisposition to Disease
- Polymorphism
- GENOME-WIDE ASSOCIATION
- Renal Insufficiency, Chronic
- Heritable
- METAANALYSIS
- Genetic Association Studies
- Science & Technology
- TRANS-EQTLS
- TRANSPORTER
- association
- genetic loci
- 06 Biological Sciences
- ta3121
- Renal Insufficiency, Chronic/genetics/physiopathology/urine
- Genetic Association Studies/methods
- 570 Life sciences; biology
- Developmental Biology
- Renal function
- Genome-Wide Association Study
詳細情報 詳細情報について
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- CRID
- 1361137044889769856
-
- ISSN
- 15461718
- 10614036
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- PubMed
- 31152163
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- データソース種別
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- Crossref
- OpenAIRE