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      Role of Uromodulin in Salt-Sensitive Hypertension

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          Abstract

          The exclusive expression of uromodulin in the kidneys has made it an intriguing protein in kidney and cardiovascular research. Genome-wide association studies discovered variants of uromodulin that are associated with chronic kidney diseases and hypertension. Urinary and circulating uromodulin levels reflect kidney and cardiovascular health as well as overall mortality. More recently, Mendelian randomization studies have shown that genetically driven levels of uromodulin have a causal and adverse effect on kidney function. On a mechanistic level, salt sensitivity is an important factor in the pathophysiology of hypertension, and uromodulin is involved in salt reabsorption via the NKCC2 (Na +-K +-2Cl cotransporter) on epithelial cells of the ascending limb of loop of Henle. In this review, we provide an overview of the multifaceted physiology and pathophysiology of uromodulin including recent advances in its genetics; cellular trafficking; and mechanistic and clinical studies undertaken to understand the complex relationship between uromodulin, blood pressure, and kidney function. We focus on tubular sodium reabsorption as one of the best understood and pathophysiologically and clinically most important roles of uromodulin, which can lead to therapeutic interventions.

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          Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

          High blood pressure is a highly heritable and modifiable risk factor for cardiovascular disease. We report the largest genetic association study of blood pressure traits (systolic, diastolic and pulse pressure) to date in over 1 million people of European ancestry. We identify 535 novel blood pressure loci that not only offer new biological insights into blood pressure regulation but also highlight shared genetic architecture between blood pressure and lifestyle exposures. Our findings identify new biological pathways for blood pressure regulation with potential for improved cardiovascular disease prevention in the future.
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            A catalog of genetic loci associated with kidney function from analyses of a million individuals

            Chronic kidney disease (CKD) is responsible for a public health burden with multi-systemic complications. Through transancestry 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.
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              Trans-ethnic association study of blood pressure determinants in over 750,000 individuals

              In this trans-ethnic multi-omic study we reinterpret the genetic architecture of blood pressure to identify genes, tissues, phenome, and medication contexts of blood pressure homeostasis. We discovered 208 novel common blood pressure SNPs and 53 rare variants in GWASs of systolic, diastolic and pulse pressure in up to 776,078 participants from the Million Veteran Program (MVP) and collaborating studies, with analysis of the blood pressure clinical phenome in MVP. Our transcriptome-wide association study detected 4,043 blood pressure associations with genetically-predicted gene expression of 840 genes in 45 tissues, and murine renal single-cell RNA sequencing identified upregulated blood pressure genes in kidney tubule cells.
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                Author and article information

                Journal
                Hypertension
                Hypertension
                HYP
                Hypertension (Dallas, Tex. : 1979)
                Lippincott Williams & Wilkins (Hagerstown, MD )
                0194-911X
                1524-4563
                12 September 2022
                November 2022
                12 September 2022
                : 79
                : 11
                : 2419-2429
                Affiliations
                [1]School of Cardiovascular and Metabolic Health, University of Glasgow, Glasgow, United Kingdom.
                Author notes
                Correspondence to: Anna Dominiczak, School of Cardiovascular and Metabolic Health, University of Glasgow, BHF Glasgow Cardiovascular Research Centre, 126 University Place, Glasgow G12 8TA, United Kingdom, Email anna.dominiczak@ 123456glasgow.ac.uk
                Christian Delles, School of Cardiovascular and Metabolic Health, University of Glasgow, BHF Glasgow Cardiovascular Research Centre, 126 University Place, Glasgow G12 8TA, United Kingdom, Email christian.delles@ 123456glasgow.ac.uk
                Author information
                https://orcid.org/0000-0001-9392-3020
                https://orcid.org/0000-0003-3595-6865
                https://orcid.org/0000-0003-3869-5808
                https://orcid.org/0000-0002-6323-124X
                https://orcid.org/0000-0002-7328-4708
                https://orcid.org/0000-0003-2238-2612
                https://orcid.org/0000-0003-4913-3608
                Article
                00006
                10.1161/HYPERTENSIONAHA.122.19888
                9553220
                36378920
                2590078c-b36f-426b-aa3b-348aeb085dc8
                © 2022 The Authors.

                Hypertension is published on behalf of the American Heart Association, Inc., by Wolters Kluwer Health, Inc. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution, and reproduction in any medium, provided that the original work is properly cited.

                This article is made available via the PMC Open Access Subset for unrestricted re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the COVID-19 pandemic or until permissions are revoked in writing. Upon expiration of these permissions, PMC is granted a perpetual license to make this article available via PMC and Europe PMC, consistent with existing copyright protections.

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                10111
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                blood pressure,kidney,loop of henle,sodium,uromodulin
                blood pressure, kidney, loop of henle, sodium, uromodulin

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