Towards Precision Medicine for Hypertension: A Review of Genomic, Epigenomic, and Microbiomic Effects on Blood Pressure in Experimental Rat Models and Humans

Compelling evidence for the inherited nature of essential hypertension has led to extensive research in rats and humans. Rats have served as the primary model for research on the genetics of hypertension resulting in identification of genomic regions that are causally associated with hypertension. I...

Celý popis

Uloženo v:
Podrobná bibliografie
Vydáno v:Physiological reviews Ročník 97; číslo 4; s. 1469
Hlavní autoři: Padmanabhan, Sandosh, Joe, Bina
Médium: Journal Article
Jazyk:angličtina
Vydáno: United States 01.10.2017
Témata:
ISSN:1522-1210, 1522-1210
On-line přístup:Zjistit podrobnosti o přístupu
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo vytvoří štítek k tomuto záznamu!
Abstract Compelling evidence for the inherited nature of essential hypertension has led to extensive research in rats and humans. Rats have served as the primary model for research on the genetics of hypertension resulting in identification of genomic regions that are causally associated with hypertension. In more recent times, genome-wide studies in humans have also begun to improve our understanding of the inheritance of polygenic forms of hypertension. Based on the chronological progression of research into the genetics of hypertension as the "structural backbone," this review catalogs and discusses the rat and human genetic elements mapped and implicated in blood pressure regulation. Furthermore, the knowledge gained from these genetic studies that provide evidence to suggest that much of the genetic influence on hypertension residing within noncoding elements of our DNA and operating through pervasive epistasis or gene-gene interactions is highlighted. Lastly, perspectives on current thinking that the more complex "triad" of the genome, epigenome, and the microbiome operating to influence the inheritance of hypertension, is documented. Overall, the collective knowledge gained from rats and humans is disappointing in the sense that major hypertension-causing genes as targets for clinical management of essential hypertension may not be a clinical reality. On the other hand, the realization that the polygenic nature of hypertension prevents any single locus from being a relevant clinical target for all humans directs future studies on the genetics of hypertension towards an individualized genomic approach.
AbstractList Compelling evidence for the inherited nature of essential hypertension has led to extensive research in rats and humans. Rats have served as the primary model for research on the genetics of hypertension resulting in identification of genomic regions that are causally associated with hypertension. In more recent times, genome-wide studies in humans have also begun to improve our understanding of the inheritance of polygenic forms of hypertension. Based on the chronological progression of research into the genetics of hypertension as the "structural backbone," this review catalogs and discusses the rat and human genetic elements mapped and implicated in blood pressure regulation. Furthermore, the knowledge gained from these genetic studies that provide evidence to suggest that much of the genetic influence on hypertension residing within noncoding elements of our DNA and operating through pervasive epistasis or gene-gene interactions is highlighted. Lastly, perspectives on current thinking that the more complex "triad" of the genome, epigenome, and the microbiome operating to influence the inheritance of hypertension, is documented. Overall, the collective knowledge gained from rats and humans is disappointing in the sense that major hypertension-causing genes as targets for clinical management of essential hypertension may not be a clinical reality. On the other hand, the realization that the polygenic nature of hypertension prevents any single locus from being a relevant clinical target for all humans directs future studies on the genetics of hypertension towards an individualized genomic approach.Compelling evidence for the inherited nature of essential hypertension has led to extensive research in rats and humans. Rats have served as the primary model for research on the genetics of hypertension resulting in identification of genomic regions that are causally associated with hypertension. In more recent times, genome-wide studies in humans have also begun to improve our understanding of the inheritance of polygenic forms of hypertension. Based on the chronological progression of research into the genetics of hypertension as the "structural backbone," this review catalogs and discusses the rat and human genetic elements mapped and implicated in blood pressure regulation. Furthermore, the knowledge gained from these genetic studies that provide evidence to suggest that much of the genetic influence on hypertension residing within noncoding elements of our DNA and operating through pervasive epistasis or gene-gene interactions is highlighted. Lastly, perspectives on current thinking that the more complex "triad" of the genome, epigenome, and the microbiome operating to influence the inheritance of hypertension, is documented. Overall, the collective knowledge gained from rats and humans is disappointing in the sense that major hypertension-causing genes as targets for clinical management of essential hypertension may not be a clinical reality. On the other hand, the realization that the polygenic nature of hypertension prevents any single locus from being a relevant clinical target for all humans directs future studies on the genetics of hypertension towards an individualized genomic approach.
Compelling evidence for the inherited nature of essential hypertension has led to extensive research in rats and humans. Rats have served as the primary model for research on the genetics of hypertension resulting in identification of genomic regions that are causally associated with hypertension. In more recent times, genome-wide studies in humans have also begun to improve our understanding of the inheritance of polygenic forms of hypertension. Based on the chronological progression of research into the genetics of hypertension as the "structural backbone," this review catalogs and discusses the rat and human genetic elements mapped and implicated in blood pressure regulation. Furthermore, the knowledge gained from these genetic studies that provide evidence to suggest that much of the genetic influence on hypertension residing within noncoding elements of our DNA and operating through pervasive epistasis or gene-gene interactions is highlighted. Lastly, perspectives on current thinking that the more complex "triad" of the genome, epigenome, and the microbiome operating to influence the inheritance of hypertension, is documented. Overall, the collective knowledge gained from rats and humans is disappointing in the sense that major hypertension-causing genes as targets for clinical management of essential hypertension may not be a clinical reality. On the other hand, the realization that the polygenic nature of hypertension prevents any single locus from being a relevant clinical target for all humans directs future studies on the genetics of hypertension towards an individualized genomic approach.
Author Padmanabhan, Sandosh
Joe, Bina
Author_xml – sequence: 1
  givenname: Sandosh
  surname: Padmanabhan
  fullname: Padmanabhan, Sandosh
  organization: Institute of Cardiovascular and Medical Sciences, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, United Kingdom; and Center for Hypertension and Personalized Medicine; Department of Physiology and Pharmacology, University of Toledo College of Medicine and Life Sciences, Toledo, Ohio
– sequence: 2
  givenname: Bina
  surname: Joe
  fullname: Joe, Bina
  organization: Institute of Cardiovascular and Medical Sciences, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, United Kingdom; and Center for Hypertension and Personalized Medicine; Department of Physiology and Pharmacology, University of Toledo College of Medicine and Life Sciences, Toledo, Ohio
BackLink https://www.ncbi.nlm.nih.gov/pubmed/28931564$$D View this record in MEDLINE/PubMed
BookMark eNpNkM1OAjEUhRujEUFfwIXp0oVgf2cYd2oQTCAagmtSOrdaM9OO7YzIw_iuDgqJq3tyz8l3c24XHTrvAKFzSgaUSnZdvW1igM8BIYTLASM0OUAnrcH6lFFy-E93UDfG9zYnZSKPUYcNM05lIk7Q98KvVcgjfg6gbbTe4RnkVlsH2PiAJ5sKQg1u69zgWzyHTwtr7A0eg_Ol1Vd4VNnXvVYuxzOrg1_Z7QKPjAFdR9xi7wrv8-2ZGJsA2Do8-mrZtgRXqwLPVY1nPoci_kImTalcPEVHRhURznazh14eRov7SX_6NH68v532tciSuq85GUqdrngyTHkKzLSdU6ayNBdcS0MBtBCpllQbAobznBORZACpEYZoLlgPXf5xq-A_Goj1srRRQ1EoB76JS5oJypMkI1kbvdhFm1UJ-bJqG6iwWe5fyn4AxON9Tw
CitedBy_id crossref_primary_10_1007_s12672_025_03323_3
crossref_primary_10_12677_MD_2018_84011
crossref_primary_10_1667_RR15536_1
crossref_primary_10_3390_biomedicines10081855
crossref_primary_10_3390_jpm12050722
crossref_primary_10_1007_s11906_018_0852_4
crossref_primary_10_3390_nu12072130
crossref_primary_10_1161_HYPERTENSIONAHA_118_12409
crossref_primary_10_14814_phy2_16165
crossref_primary_10_1002_advs_201801039
crossref_primary_10_1007_s12291_022_01041_z
crossref_primary_10_7717_peerj_9849
crossref_primary_10_1093_nar_gkac912
crossref_primary_10_1093_ajh_hpaa166
crossref_primary_10_1097_HJH_0000000000001732
crossref_primary_10_1177_00368504221101636
crossref_primary_10_1016_j_cjca_2019_02_003
crossref_primary_10_1111_joim_13352
crossref_primary_10_3390_ijms21134709
crossref_primary_10_1016_j_archger_2025_105992
crossref_primary_10_1007_s00109_020_02002_w
crossref_primary_10_1038_s41419_021_03462_9
crossref_primary_10_1093_function_zqae045
crossref_primary_10_1038_s41598_021_84135_7
crossref_primary_10_1007_s40266_022_00966_7
crossref_primary_10_1038_s41401_021_00772_8
crossref_primary_10_3390_biomedicines10040875
crossref_primary_10_1186_s12864_023_09757_9
crossref_primary_10_1161_HYPERTENSIONAHA_124_21721
crossref_primary_10_1152_ajprenal_00359_2019
crossref_primary_10_1161_HYP_0000000000000090
crossref_primary_10_3389_fphar_2018_00168
crossref_primary_10_1016_j_cjca_2020_03_001
crossref_primary_10_1093_advances_nmz064
crossref_primary_10_1016_j_intimp_2020_106277
crossref_primary_10_1038_s41569_020_00466_4
crossref_primary_10_1002_j_2040_4603_2019_tb00095_x
crossref_primary_10_1161_CIRCRESAHA_119_314403
crossref_primary_10_1161_HYPERTENSIONAHA_120_15880
crossref_primary_10_1161_HYPERTENSIONAHA_120_14830
crossref_primary_10_1016_j_vph_2019_106633
crossref_primary_10_1038_s41598_020_58540_3
crossref_primary_10_3389_fcvm_2022_814502
crossref_primary_10_1002_j_2040_4603_2020_tb00115_x
crossref_primary_10_1016_j_drudis_2019_01_009
crossref_primary_10_1155_2020_9185697
crossref_primary_10_1038_s41440_022_00885_5
crossref_primary_10_1016_j_ctcp_2022_101641
crossref_primary_10_1155_2022_5849736
crossref_primary_10_1007_s44200_022_00016_y
crossref_primary_10_1161_HYPERTENSIONAHA_122_19307
crossref_primary_10_3389_fphar_2022_1045501
crossref_primary_10_1038_sdata_2018_284
crossref_primary_10_1161_HYPERTENSIONAHA_119_14109
crossref_primary_10_1161_HYPERTENSIONAHA_119_12723
crossref_primary_10_3389_fcvm_2022_888569
crossref_primary_10_1161_HYPERTENSIONAHA_125_24002
crossref_primary_10_1371_journal_pone_0221658
crossref_primary_10_1161_HYPERTENSIONAHA_124_23122
crossref_primary_10_3389_fgene_2023_1114174
crossref_primary_10_1093_ajh_hpaa022
crossref_primary_10_1152_ajpregu_00449_2017
crossref_primary_10_1007_s11906_022_01226_0
crossref_primary_10_1016_j_cyto_2023_156293
crossref_primary_10_1152_ajprenal_00624_2018
crossref_primary_10_1161_HYPERTENSIONAHA_125_17950
crossref_primary_10_1007_s11906_018_0863_1
crossref_primary_10_1161_HYPERTENSIONAHA_120_13896
crossref_primary_10_1016_j_ejphar_2024_176467
crossref_primary_10_1007_s11906_024_01315_2
crossref_primary_10_1093_cvr_cvaa164
crossref_primary_10_1016_j_ctim_2022_102818
crossref_primary_10_1016_j_ejphar_2024_176907
crossref_primary_10_1007_s11906_021_01157_2
crossref_primary_10_1242_dmm_048090
crossref_primary_10_1080_14622416_2025_2504865
crossref_primary_10_1016_j_ebiom_2022_104243
ContentType Journal Article
Copyright Copyright © 2017 the American Physiological Society.
Copyright_xml – notice: Copyright © 2017 the American Physiological Society.
DBID CGR
CUY
CVF
ECM
EIF
NPM
7X8
DOI 10.1152/physrev.00035.2016
DatabaseName Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
MEDLINE - Academic
DatabaseTitle MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
MEDLINE - Academic
DatabaseTitleList MEDLINE - Academic
MEDLINE
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: 7X8
  name: MEDLINE - Academic
  url: https://search.proquest.com/medline
  sourceTypes: Aggregation Database
DeliveryMethod no_fulltext_linktorsrc
Discipline Medicine
Anatomy & Physiology
EISSN 1522-1210
ExternalDocumentID 28931564
Genre Review
Research Support, Non-U.S. Gov't
Journal Article
Research Support, N.I.H., Extramural
GrantInformation_xml – fundername: British Heart Foundation
  grantid: SP/14/8/31352
– fundername: British Heart Foundation
  grantid: CS/16/1/31878
– fundername: British Heart Foundation
  grantid: PG/12/85/29925
– fundername: NHLBI NIH HHS
  grantid: R01 HL112641
– fundername: Medical Research Council
  grantid: MR/M016560/1
GroupedDBID ---
-DZ
-~X
.55
123
18M
2WC
4.4
53G
5VS
79B
85S
AAFWJ
AAYJJ
ABCQX
ABHWK
ABJNI
ABKWE
ABOCM
ABPPZ
ACGFO
ACGFS
ACGOD
ACNCT
ACPRK
ADBBV
ADFNX
ADIYS
AENEX
AETEA
AGHSJ
ALMA_UNASSIGNED_HOLDINGS
BAWUL
BKKCC
BTFSW
CGR
CS3
CUY
CVF
DIK
DU5
E3Z
EBS
ECM
EIF
EJD
EMOBN
F5P
GX1
H13
H~9
IH2
IHR
IOF
ITBOX
KQ8
L7B
N9A
NHB
NPM
OK1
P2P
PQQKQ
RAP
RHI
RPL
RPRKH
RWL
RXW
TAE
TN5
TR2
W8F
WH7
WOQ
X7M
XSW
YBH
YNT
YSK
ZCA
7X8
ID FETCH-LOGICAL-c496t-c3085c7b368737e2f12172a97d43c5f1eec447c51cf0ef33d30469ee7f4f0c342
IEDL.DBID 7X8
ISICitedReferencesCount 89
ISICitedReferencesURI http://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestLinkType=CitingArticles&DestApp=WOS_CPL&KeyUT=000423335500005&url=https%3A%2F%2Fcvtisr.summon.serialssolutions.com%2F%23%21%2Fsearch%3Fho%3Df%26include.ft.matches%3Dt%26l%3Dnull%26q%3D
ISSN 1522-1210
IngestDate Thu Oct 02 05:49:44 EDT 2025
Sat May 31 02:06:04 EDT 2025
IsDoiOpenAccess false
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 4
Language English
License Copyright © 2017 the American Physiological Society.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c496t-c3085c7b368737e2f12172a97d43c5f1eec447c51cf0ef33d30469ee7f4f0c342
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
ObjectType-Review-3
content type line 23
OpenAccessLink https://www.ncbi.nlm.nih.gov/pmc/articles/6347103
PMID 28931564
PQID 1941366909
PQPubID 23479
ParticipantIDs proquest_miscellaneous_1941366909
pubmed_primary_28931564
PublicationCentury 2000
PublicationDate 2017-10-01
PublicationDateYYYYMMDD 2017-10-01
PublicationDate_xml – month: 10
  year: 2017
  text: 2017-10-01
  day: 01
PublicationDecade 2010
PublicationPlace United States
PublicationPlace_xml – name: United States
PublicationTitle Physiological reviews
PublicationTitleAlternate Physiol Rev
PublicationYear 2017
SSID ssj0005565
Score 2.5410626
SecondaryResourceType review_article
Snippet Compelling evidence for the inherited nature of essential hypertension has led to extensive research in rats and humans. Rats have served as the primary model...
SourceID proquest
pubmed
SourceType Aggregation Database
Index Database
StartPage 1469
SubjectTerms Animals
Epigenesis, Genetic
Genome - physiology
Humans
Hypertension - genetics
Hypertension - microbiology
Hypertension - pathology
Microbiota
Rats
Title Towards Precision Medicine for Hypertension: A Review of Genomic, Epigenomic, and Microbiomic Effects on Blood Pressure in Experimental Rat Models and Humans
URI https://www.ncbi.nlm.nih.gov/pubmed/28931564
https://www.proquest.com/docview/1941366909
Volume 97
WOSCitedRecordID wos000423335500005&url=https%3A%2F%2Fcvtisr.summon.serialssolutions.com%2F%23%21%2Fsearch%3Fho%3Df%26include.ft.matches%3Dt%26l%3Dnull%26q%3D
hasFullText
inHoldings 1
isFullTextHit
isPrint
link http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1bS8MwFA7eEF-8zcu8cQTxybKlSZPFF5ky3cvGEIW9jTZNYKDtXKfgj_G_epJ2zBdB8KWUhobCOU3OOd-X8xFywawRCbc6UIkQAQ-1ChRTLEhCaVVKlaQ88WITst9vDYdqUBXciopWOV8T_UKd5trVyBuYbFMmMJdTN5O3wKlGOXS1ktBYJqsMQxnn1XK46BYeRV5KErcoJ-BBm_NDM1HYcHUDJ_LioTTH8BK_h5h-q7nf-u9HbpPNKsiEdukVO2TJZLuk1s4wwX79hEvwtE9fT98l670KXa-RryfPoS1gMK2Ud2A-CBjbQhdz1qlnvOfZNbShxBUgt_Bg_OnmK-hMfNdXfx9nKfTGZaMnfABlo-QCcNpbR5eH8mji1MA4g84PpQF4jGfgRNpeCj-JBxqKPfJ833m66waVfEOguRKzQDMM57RMmGhJJk1oqRPDipVMOdORpcZozqWOqLZNYxlLHUirjJGW26ZmPNwnK1memUMCiUavicNQWYYZFhMJtVKkHL1PUN1KZZ2cz-0xwt_DYR5xZvL3YrSwSJ0clEYdTco-HiPMNZnrlXP0h7ePyUboNnRP4zshqxYXB3NK1vTHbFxMz7zf4bU_6H0DQwLkFA
linkProvider ProQuest
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Towards+Precision+Medicine+for+Hypertension%3A+A+Review+of+Genomic%2C+Epigenomic%2C+and+Microbiomic+Effects+on+Blood+Pressure+in+Experimental+Rat+Models+and+Humans&rft.jtitle=Physiological+reviews&rft.au=Padmanabhan%2C+Sandosh&rft.au=Joe%2C+Bina&rft.date=2017-10-01&rft.issn=1522-1210&rft.eissn=1522-1210&rft.volume=97&rft.issue=4&rft.spage=1469&rft_id=info:doi/10.1152%2Fphysrev.00035.2016&rft.externalDBID=NO_FULL_TEXT
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1522-1210&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1522-1210&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1522-1210&client=summon