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...
Gespeichert in:
Veröffentlicht in: | Nature medicine 2013-12, Vol.19 (12), p.1655-1660 |
---|---|
Hauptverfasser: | , , , , , , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
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 |
format | Article |
fullrecord | <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3856354</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A353323181</galeid><sourcerecordid>A353323181</sourcerecordid><originalsourceid>FETCH-LOGICAL-c733t-eda3053ef01329825906e662d16443aed3691b60e885706c225c0bda4941b4303</originalsourceid><addsrcrecordid>eNqNkltrFDEYhgdRbK3iP5CA4OFi1mRy2JmbQtlWLVQW1Ip3IZt8O5s6k6zJzNIFf7wZWtudsheSi5ye983h_bLsJcETgmn5wbUTSkv2KDsknImcTPHPx2mMp2VeVlwcZM9ivMIYU8yrp9lBwUjJRUUPsz8z37beIeed9sa6Gl1-mZ-iGhygjQpWuS4i60yvAUXVdHkEF21nN4BW2zWEbpgmvXIG_bLGwRYZ1aoa0GKbdDqAioNrH3zrTd9Yh-B6HSAOqufZk6VqIry47Y-yy49n32ef84v5p_PZyUWup5R2ORiV7k1hiQktqrLgFRYgRGGIYIwqMFRUZCEwlCWfYqGLgmu8MIpVjCwYxfQoO77xXfeLFowG1wXVyHWwrQpb6ZWV4x1nV7L2G0nTL1HOksG7W4Pgf_cQO9naqKFplAPfR0m4ECUjgoqEvn6AXvk-uPQ8SZjglJCiwvdUrRqQ1i19OlcPpvKEckoLSkqSqHwPNWSTLukdLG1aHvGTPXxqBlqr9wrejwSJ6eC6q1Ufozz_9vX_2fmPMftmh11BKpxV9E3fpdDjGHx7A-rgYwywvAuFYDlUtnStHCo7ka92M7zj_pXyfUYxbbkaws7HP_D6C7wO_f8</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1465311290</pqid></control><display><type>article</type><title>Common noncoding UMOD gene variants induce salt-sensitive hypertension and kidney damage by increasing uromodulin expression</title><source>MEDLINE</source><source>SpringerLink Journals</source><source>Nature Journals Online</source><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</creator><creatorcontrib>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 ; SKIPOGH team ; the Swiss Kidney Project on Genes in Hypertension (SKIPOGH) team</creatorcontrib><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.</description><identifier>ISSN: 1078-8956</identifier><identifier>EISSN: 1546-170X</identifier><identifier>DOI: 10.1038/nm.3384</identifier><identifier>PMID: 24185693</identifier><language>eng</language><publisher>New York: Nature Publishing Group US</publisher><subject>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</subject><ispartof>Nature medicine, 2013-12, Vol.19 (12), p.1655-1660</ispartof><rights>Springer Nature America, Inc. 2013</rights><rights>COPYRIGHT 2013 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Dec 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c733t-eda3053ef01329825906e662d16443aed3691b60e885706c225c0bda4941b4303</citedby><cites>FETCH-LOGICAL-c733t-eda3053ef01329825906e662d16443aed3691b60e885706c225c0bda4941b4303</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/nm.3384$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/nm.3384$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>230,314,776,780,881,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24185693$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Trudu, Matteo</creatorcontrib><creatorcontrib>Janas, Sylvie</creatorcontrib><creatorcontrib>Lanzani, Chiara</creatorcontrib><creatorcontrib>Debaix, Huguette</creatorcontrib><creatorcontrib>Schaeffer, Céline</creatorcontrib><creatorcontrib>Ikehata, Masami</creatorcontrib><creatorcontrib>Citterio, Lorena</creatorcontrib><creatorcontrib>Demaretz, Sylvie</creatorcontrib><creatorcontrib>Trevisani, Francesco</creatorcontrib><creatorcontrib>Ristagno, Giuseppe</creatorcontrib><creatorcontrib>Glaudemans, Bob</creatorcontrib><creatorcontrib>Laghmani, Kamel</creatorcontrib><creatorcontrib>Dell'Antonio, Giacomo</creatorcontrib><creatorcontrib>Loffing, Johannes</creatorcontrib><creatorcontrib>Rastaldi, Maria P</creatorcontrib><creatorcontrib>Manunta, Paolo</creatorcontrib><creatorcontrib>Devuyst, Olivier</creatorcontrib><creatorcontrib>Rampoldi, Luca</creatorcontrib><creatorcontrib>SKIPOGH team</creatorcontrib><creatorcontrib>the Swiss Kidney Project on Genes in Hypertension (SKIPOGH) team</creatorcontrib><title>Common noncoding UMOD gene variants induce salt-sensitive hypertension and kidney damage by increasing uromodulin expression</title><title>Nature medicine</title><addtitle>Nat Med</addtitle><addtitle>Nat Med</addtitle><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.</description><subject>13/1</subject><subject>13/109</subject><subject>13/44</subject><subject>13/51</subject><subject>14/19</subject><subject>14/34</subject><subject>14/63</subject><subject>38/77</subject><subject>45/22</subject><subject>45/90</subject><subject>692/308/1426</subject><subject>692/499</subject><subject>692/699/1585/104</subject><subject>692/699/75/243</subject><subject>82</subject><subject>82/29</subject><subject>82/80</subject><subject>Adult</subject><subject>Aged</subject><subject>Animals</subject><subject>Biomedicine</subject><subject>Blood pressure</subject><subject>Cancer Research</subject><subject>Diagnosis</subject><subject>Female</subject><subject>Gene expression</subject><subject>Gene Expression Regulation</subject><subject>Genetic aspects</subject><subject>Genetic diversity</subject><subject>Genetic Predisposition to Disease</subject><subject>Genome-Wide Association Study</subject><subject>Global health</subject><subject>Glycoproteins</subject><subject>Health problems</subject><subject>Humans</subject><subject>Hypertension</subject><subject>Hypertension - chemically induced</subject><subject>Hypertension - genetics</subject><subject>Infectious Diseases</subject><subject>Kidney diseases</subject><subject>Kidneys</subject><subject>Lesions</subject><subject>letter</subject><subject>Male</subject><subject>Metabolic Diseases</subject><subject>Mice</subject><subject>Mice, Transgenic</subject><subject>Middle Aged</subject><subject>Molecular Medicine</subject><subject>Neurosciences</subject><subject>Noncoding DNA</subject><subject>Physiological aspects</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Promoter Regions, Genetic - genetics</subject><subject>Properties</subject><subject>Renal function</subject><subject>Renal Insufficiency, Chronic - genetics</subject><subject>Salts</subject><subject>Sodium</subject><subject>Sodium, Dietary - adverse effects</subject><subject>Sodium, Dietary - pharmacokinetics</subject><subject>Studies</subject><subject>Up-Regulation</subject><subject>Uromodulin - genetics</subject><subject>Young Adult</subject><issn>1078-8956</issn><issn>1546-170X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqNkltrFDEYhgdRbK3iP5CA4OFi1mRy2JmbQtlWLVQW1Ip3IZt8O5s6k6zJzNIFf7wZWtudsheSi5ye983h_bLsJcETgmn5wbUTSkv2KDsknImcTPHPx2mMp2VeVlwcZM9ivMIYU8yrp9lBwUjJRUUPsz8z37beIeed9sa6Gl1-mZ-iGhygjQpWuS4i60yvAUXVdHkEF21nN4BW2zWEbpgmvXIG_bLGwRYZ1aoa0GKbdDqAioNrH3zrTd9Yh-B6HSAOqufZk6VqIry47Y-yy49n32ef84v5p_PZyUWup5R2ORiV7k1hiQktqrLgFRYgRGGIYIwqMFRUZCEwlCWfYqGLgmu8MIpVjCwYxfQoO77xXfeLFowG1wXVyHWwrQpb6ZWV4x1nV7L2G0nTL1HOksG7W4Pgf_cQO9naqKFplAPfR0m4ECUjgoqEvn6AXvk-uPQ8SZjglJCiwvdUrRqQ1i19OlcPpvKEckoLSkqSqHwPNWSTLukdLG1aHvGTPXxqBlqr9wrejwSJ6eC6q1Ufozz_9vX_2fmPMftmh11BKpxV9E3fpdDjGHx7A-rgYwywvAuFYDlUtnStHCo7ka92M7zj_pXyfUYxbbkaws7HP_D6C7wO_f8</recordid><startdate>20131201</startdate><enddate>20131201</enddate><creator>Trudu, Matteo</creator><creator>Janas, Sylvie</creator><creator>Lanzani, Chiara</creator><creator>Debaix, Huguette</creator><creator>Schaeffer, Céline</creator><creator>Ikehata, Masami</creator><creator>Citterio, Lorena</creator><creator>Demaretz, Sylvie</creator><creator>Trevisani, Francesco</creator><creator>Ristagno, Giuseppe</creator><creator>Glaudemans, Bob</creator><creator>Laghmani, Kamel</creator><creator>Dell'Antonio, Giacomo</creator><creator>Loffing, Johannes</creator><creator>Rastaldi, Maria P</creator><creator>Manunta, Paolo</creator><creator>Devuyst, Olivier</creator><creator>Rampoldi, Luca</creator><general>Nature Publishing Group US</general><general>Nature Publishing Group</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U7</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>MBDVC</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>RC3</scope><scope>5PM</scope></search><sort><creationdate>20131201</creationdate><title>Common noncoding UMOD gene variants induce salt-sensitive hypertension and kidney damage by increasing uromodulin expression</title><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c733t-eda3053ef01329825906e662d16443aed3691b60e885706c225c0bda4941b4303</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>13/1</topic><topic>13/109</topic><topic>13/44</topic><topic>13/51</topic><topic>14/19</topic><topic>14/34</topic><topic>14/63</topic><topic>38/77</topic><topic>45/22</topic><topic>45/90</topic><topic>692/308/1426</topic><topic>692/499</topic><topic>692/699/1585/104</topic><topic>692/699/75/243</topic><topic>82</topic><topic>82/29</topic><topic>82/80</topic><topic>Adult</topic><topic>Aged</topic><topic>Animals</topic><topic>Biomedicine</topic><topic>Blood pressure</topic><topic>Cancer Research</topic><topic>Diagnosis</topic><topic>Female</topic><topic>Gene expression</topic><topic>Gene Expression Regulation</topic><topic>Genetic aspects</topic><topic>Genetic diversity</topic><topic>Genetic Predisposition to Disease</topic><topic>Genome-Wide Association Study</topic><topic>Global health</topic><topic>Glycoproteins</topic><topic>Health problems</topic><topic>Humans</topic><topic>Hypertension</topic><topic>Hypertension - chemically induced</topic><topic>Hypertension - genetics</topic><topic>Infectious Diseases</topic><topic>Kidney diseases</topic><topic>Kidneys</topic><topic>Lesions</topic><topic>letter</topic><topic>Male</topic><topic>Metabolic Diseases</topic><topic>Mice</topic><topic>Mice, Transgenic</topic><topic>Middle Aged</topic><topic>Molecular Medicine</topic><topic>Neurosciences</topic><topic>Noncoding DNA</topic><topic>Physiological aspects</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Promoter Regions, Genetic - genetics</topic><topic>Properties</topic><topic>Renal function</topic><topic>Renal Insufficiency, Chronic - genetics</topic><topic>Salts</topic><topic>Sodium</topic><topic>Sodium, Dietary - adverse effects</topic><topic>Sodium, Dietary - pharmacokinetics</topic><topic>Studies</topic><topic>Up-Regulation</topic><topic>Uromodulin - genetics</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Trudu, Matteo</creatorcontrib><creatorcontrib>Janas, Sylvie</creatorcontrib><creatorcontrib>Lanzani, Chiara</creatorcontrib><creatorcontrib>Debaix, Huguette</creatorcontrib><creatorcontrib>Schaeffer, Céline</creatorcontrib><creatorcontrib>Ikehata, Masami</creatorcontrib><creatorcontrib>Citterio, Lorena</creatorcontrib><creatorcontrib>Demaretz, Sylvie</creatorcontrib><creatorcontrib>Trevisani, Francesco</creatorcontrib><creatorcontrib>Ristagno, Giuseppe</creatorcontrib><creatorcontrib>Glaudemans, Bob</creatorcontrib><creatorcontrib>Laghmani, Kamel</creatorcontrib><creatorcontrib>Dell'Antonio, Giacomo</creatorcontrib><creatorcontrib>Loffing, Johannes</creatorcontrib><creatorcontrib>Rastaldi, Maria P</creatorcontrib><creatorcontrib>Manunta, Paolo</creatorcontrib><creatorcontrib>Devuyst, Olivier</creatorcontrib><creatorcontrib>Rampoldi, Luca</creatorcontrib><creatorcontrib>SKIPOGH team</creatorcontrib><creatorcontrib>the Swiss Kidney Project on Genes in Hypertension (SKIPOGH) team</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & 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> |
fulltext | fulltext |
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 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-09T20%3A22%3A58IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Common%20noncoding%20UMOD%20gene%20variants%20induce%20salt-sensitive%20hypertension%20and%20kidney%20damage%20by%20increasing%20uromodulin%20expression&rft.jtitle=Nature%20medicine&rft.au=Trudu,%20Matteo&rft.aucorp=SKIPOGH%20team&rft.date=2013-12-01&rft.volume=19&rft.issue=12&rft.spage=1655&rft.epage=1660&rft.pages=1655-1660&rft.issn=1078-8956&rft.eissn=1546-170X&rft_id=info:doi/10.1038/nm.3384&rft_dat=%3Cgale_pubme%3EA353323181%3C/gale_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1465311290&rft_id=info:pmid/24185693&rft_galeid=A353323181&rfr_iscdi=true |