Common noncoding UMOD gene variants induce salt-sensitive hypertension and kidney damage by increasing uromodulin expression

Variation in the promoter of the gene encoding uromodulin, the most abundant protein in urine, affects the individual risk of developing hypertension or chronic kidney disease. Luca Rampoldi, Olivier Devuyst and their colleagues show that the uromodulin risk alleles are associated with higher levels...

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Veröffentlicht in:Nature medicine 2013-12, Vol.19 (12), p.1655-1660
Hauptverfasser: Trudu, Matteo, Janas, Sylvie, Lanzani, Chiara, Debaix, Huguette, Schaeffer, Céline, Ikehata, Masami, Citterio, Lorena, Demaretz, Sylvie, Trevisani, Francesco, Ristagno, Giuseppe, Glaudemans, Bob, Laghmani, Kamel, Dell'Antonio, Giacomo, Loffing, Johannes, Rastaldi, Maria P, Manunta, Paolo, Devuyst, Olivier, Rampoldi, Luca
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container_end_page 1660
container_issue 12
container_start_page 1655
container_title Nature medicine
container_volume 19
creator Trudu, Matteo
Janas, Sylvie
Lanzani, Chiara
Debaix, Huguette
Schaeffer, Céline
Ikehata, Masami
Citterio, Lorena
Demaretz, Sylvie
Trevisani, Francesco
Ristagno, Giuseppe
Glaudemans, Bob
Laghmani, Kamel
Dell'Antonio, Giacomo
Loffing, Johannes
Rastaldi, Maria P
Manunta, Paolo
Devuyst, Olivier
Rampoldi, Luca
description Variation in the promoter of the gene encoding uromodulin, the most abundant protein in urine, affects the individual risk of developing hypertension or chronic kidney disease. Luca Rampoldi, Olivier Devuyst and their colleagues show that the uromodulin risk alleles are associated with higher levels of uromodulin expression. This can promote hypertension, by stimulating sodium reabsorption by the loop of Henle in the kidney, and kidney damage in both mice and humans. Hypertension and chronic kidney disease (CKD) are complex traits representing major global health problems 1 , 2 . Multiple genome-wide association studies have identified common variants in the promoter of the UMOD gene 3 , 4 , 5 , 6 , 7 , 8 , 9 , which encodes uromodulin, the major protein secreted in normal urine, that cause independent susceptibility to CKD and hypertension. Despite compelling genetic evidence for the association between UMOD risk variants and disease susceptibility in the general population, the underlying biological mechanism is not understood. Here, we demonstrate that UMOD risk variants increased UMOD expression in vitro and in vivo . Uromodulin overexpression in transgenic mice led to salt-sensitive hypertension and to the presence of age-dependent renal lesions similar to those observed in elderly individuals homozygous for UMOD promoter risk variants. The link between uromodulin and hypertension is due to activation of the renal sodium cotransporter NKCC2. We demonstrated the relevance of this mechanism in humans by showing that pharmacological inhibition of NKCC2 was more effective in lowering blood pressure in hypertensive patients who are homozygous for UMOD promoter risk variants than in other hypertensive patients. Our findings link genetic susceptibility to hypertension and CKD to the level of uromodulin expression and uromodulin's effect on salt reabsorption in the kidney. These findings point to uromodulin as a therapeutic target for lowering blood pressure and preserving renal function.
doi_str_mv 10.1038/nm.3384
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Uromodulin overexpression in transgenic mice led to salt-sensitive hypertension and to the presence of age-dependent renal lesions similar to those observed in elderly individuals homozygous for UMOD promoter risk variants. The link between uromodulin and hypertension is due to activation of the renal sodium cotransporter NKCC2. We demonstrated the relevance of this mechanism in humans by showing that pharmacological inhibition of NKCC2 was more effective in lowering blood pressure in hypertensive patients who are homozygous for UMOD promoter risk variants than in other hypertensive patients. Our findings link genetic susceptibility to hypertension and CKD to the level of uromodulin expression and uromodulin's effect on salt reabsorption in the kidney. 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Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Nature medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Trudu, Matteo</au><au>Janas, Sylvie</au><au>Lanzani, Chiara</au><au>Debaix, Huguette</au><au>Schaeffer, Céline</au><au>Ikehata, Masami</au><au>Citterio, Lorena</au><au>Demaretz, Sylvie</au><au>Trevisani, Francesco</au><au>Ristagno, Giuseppe</au><au>Glaudemans, Bob</au><au>Laghmani, Kamel</au><au>Dell'Antonio, Giacomo</au><au>Loffing, Johannes</au><au>Rastaldi, Maria P</au><au>Manunta, Paolo</au><au>Devuyst, Olivier</au><au>Rampoldi, Luca</au><aucorp>SKIPOGH team</aucorp><aucorp>the Swiss Kidney Project on Genes in Hypertension (SKIPOGH) team</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Common noncoding UMOD gene variants induce salt-sensitive hypertension and kidney damage by increasing uromodulin expression</atitle><jtitle>Nature medicine</jtitle><stitle>Nat Med</stitle><addtitle>Nat Med</addtitle><date>2013-12-01</date><risdate>2013</risdate><volume>19</volume><issue>12</issue><spage>1655</spage><epage>1660</epage><pages>1655-1660</pages><issn>1078-8956</issn><eissn>1546-170X</eissn><abstract>Variation in the promoter of the gene encoding uromodulin, the most abundant protein in urine, affects the individual risk of developing hypertension or chronic kidney disease. Luca Rampoldi, Olivier Devuyst and their colleagues show that the uromodulin risk alleles are associated with higher levels of uromodulin expression. This can promote hypertension, by stimulating sodium reabsorption by the loop of Henle in the kidney, and kidney damage in both mice and humans. Hypertension and chronic kidney disease (CKD) are complex traits representing major global health problems 1 , 2 . Multiple genome-wide association studies have identified common variants in the promoter of the UMOD gene 3 , 4 , 5 , 6 , 7 , 8 , 9 , which encodes uromodulin, the major protein secreted in normal urine, that cause independent susceptibility to CKD and hypertension. Despite compelling genetic evidence for the association between UMOD risk variants and disease susceptibility in the general population, the underlying biological mechanism is not understood. Here, we demonstrate that UMOD risk variants increased UMOD expression in vitro and in vivo . Uromodulin overexpression in transgenic mice led to salt-sensitive hypertension and to the presence of age-dependent renal lesions similar to those observed in elderly individuals homozygous for UMOD promoter risk variants. The link between uromodulin and hypertension is due to activation of the renal sodium cotransporter NKCC2. We demonstrated the relevance of this mechanism in humans by showing that pharmacological inhibition of NKCC2 was more effective in lowering blood pressure in hypertensive patients who are homozygous for UMOD promoter risk variants than in other hypertensive patients. Our findings link genetic susceptibility to hypertension and CKD to the level of uromodulin expression and uromodulin's effect on salt reabsorption in the kidney. These findings point to uromodulin as a therapeutic target for lowering blood pressure and preserving renal function.</abstract><cop>New York</cop><pub>Nature Publishing Group US</pub><pmid>24185693</pmid><doi>10.1038/nm.3384</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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identifier ISSN: 1078-8956
ispartof Nature medicine, 2013-12, Vol.19 (12), p.1655-1660
issn 1078-8956
1546-170X
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3856354
source MEDLINE; SpringerLink Journals; Nature Journals Online
subjects 13/1
13/109
13/44
13/51
14/19
14/34
14/63
38/77
45/22
45/90
692/308/1426
692/499
692/699/1585/104
692/699/75/243
82
82/29
82/80
Adult
Aged
Animals
Biomedicine
Blood pressure
Cancer Research
Diagnosis
Female
Gene expression
Gene Expression Regulation
Genetic aspects
Genetic diversity
Genetic Predisposition to Disease
Genome-Wide Association Study
Global health
Glycoproteins
Health problems
Humans
Hypertension
Hypertension - chemically induced
Hypertension - genetics
Infectious Diseases
Kidney diseases
Kidneys
Lesions
letter
Male
Metabolic Diseases
Mice
Mice, Transgenic
Middle Aged
Molecular Medicine
Neurosciences
Noncoding DNA
Physiological aspects
Polymorphism, Single Nucleotide
Promoter Regions, Genetic - genetics
Properties
Renal function
Renal Insufficiency, Chronic - genetics
Salts
Sodium
Sodium, Dietary - adverse effects
Sodium, Dietary - pharmacokinetics
Studies
Up-Regulation
Uromodulin - genetics
Young Adult
title Common noncoding UMOD gene variants induce salt-sensitive hypertension and kidney damage by increasing uromodulin expression
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