Association Between aquaporin-1 and Endurance Performance: A Systematic Review
Background There is abundant and mounting information related to the molecular and biological structure and function of the Aquaporin-1 ( AQP1 ) gene and the AQP1-Aquaporin channel. Regulation of water flow across cell membranes is essential for supporting inter- and intracellular fluid balance, whi...
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description | Background
There is abundant and mounting information related to the molecular and biological structure and function of the
Aquaporin-1
(
AQP1
) gene and the AQP1-Aquaporin channel. Regulation of water flow across cell membranes is essential for supporting inter- and intracellular fluid balance, which is critical for health and exercise performance. The transmembrane water channel AQP1 is important for cardiorespiratory endurance (CE) because it influences fluid transfers in erythrocytes, endothelial, and pulmonary cells and is vital for transport of ammonium, bicarbonate, carbon dioxide, glycerol, nitric oxide, potassium ion, water, and trans-epithelial and renal water. Very recent publications suggest the association between a DNA sequence variant, rs1049305 (C > G), in the 3′-untranslated region of the
AQP1
gene and CE performance. Other reports indicate further significant associations between AQP1 channel and CE phenotypes. The purposes of this systematic review were to examine the extent of the associations between the
AQP1
rs1049305 genotype and CE exercise performance and body fluid loss in long-distance runners and AQP1 channel associations with other CE phenotypes.
Methods
Data sources: A comprehensive review was conducted using PubMed, EMBASE, CINAHL, and Cochrane electronic databases. The search ranged from January 1, 1988, to December 31, 2018. Studies reported in English, French, and Spanish were considered. Eligibility criteria: The criteria for inclusion in the review were (a) case-control study; (b) unequivocal definition of cases and controls; (c) CE was defined as performance in endurance events, laboratory tests, and/or maximal oxygen consumption; (d) exclusion criteria of known causes; (e) genotyping performed by PCR or sequencing; (f) genotype frequencies reported; and (g) no deviation of genotype frequencies from Hardy-Weinberg equilibrium in the control group. Study appraisal: The systematic review included studies examining the
AQP1
gene and AQP1 channel structure and function, associations between the
AQP1
gene sequence variant rs1049305 (C > G) and CE performance, body fluid loss in long-distance runners, and other studies reporting on the
AQP1
gene and channel CE phenotype associations. Synthesis methods: For each selected study, the following data were extracted: authors, year of publication, sample size and number of cases and controls, CE definition, exclusion criteria, inclusion criteria for cases and controls, methods used |
doi_str_mv | 10.1186/s40798-019-0213-0 |
format | Article |
fullrecord | <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6728102</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A598567773</galeid><sourcerecordid>A598567773</sourcerecordid><originalsourceid>FETCH-LOGICAL-c509t-65cb7e32b78216a47729efb666ca24f545cad4c1bde377c48ebb83a55783fee93</originalsourceid><addsrcrecordid>eNp1UctuFDEQtBCIREs-gAsaifMkfj84IC1RSCJFEAU4Wx5Pz2K0Y2_smUT5e7xMCHBAPrjVXVVddiH0muBjQrQ8KRwro1tMTIspYS1-hg4pqR2jJHn-qzYtIQofoKNSQocF5pwzzF6iA0a4lobqQ_RpXUrywU0hxeYDTPcAsXG3s9ulHGJLGhf75iz2c3bRQ3MNeUh53NfvmnXz5aFMMFayb27gLsD9K_RicNsCR4_3Cn37ePb19KK9-nx-ebq-ar3AZmql8J0CRjulKZGOK0UNDJ2U0jvKB8GFdz33pOuBKeW5hq7TzAmhNBsADFuh94vubu5G6D3EKbut3eUwuvxgkwv230kM3-0m3VmpqCaYVoG3jwI53c5QJvsjzTlWz5ZSzbXm-09doeMFtXFbsCEOqYr5enoYg08RhlD7a2G0kEopVglkIficSskwPFki2O5js0tstsZm9xssrpw3f7_lifE7pAqgC6DUUdxA_uP1_6o_AbL9ozg</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2284884021</pqid></control><display><type>article</type><title>Association Between aquaporin-1 and Endurance Performance: A Systematic Review</title><source>Springer Online Journals Complete</source><source>DOAJ Directory of Open Access Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><source>Springer Nature OA/Free Journals</source><source>PubMed Central Open Access</source><creator>Rivera, Miguel A. ; Fahey, Thomas D.</creator><creatorcontrib>Rivera, Miguel A. ; Fahey, Thomas D.</creatorcontrib><description>Background
There is abundant and mounting information related to the molecular and biological structure and function of the
Aquaporin-1
(
AQP1
) gene and the AQP1-Aquaporin channel. Regulation of water flow across cell membranes is essential for supporting inter- and intracellular fluid balance, which is critical for health and exercise performance. The transmembrane water channel AQP1 is important for cardiorespiratory endurance (CE) because it influences fluid transfers in erythrocytes, endothelial, and pulmonary cells and is vital for transport of ammonium, bicarbonate, carbon dioxide, glycerol, nitric oxide, potassium ion, water, and trans-epithelial and renal water. Very recent publications suggest the association between a DNA sequence variant, rs1049305 (C > G), in the 3′-untranslated region of the
AQP1
gene and CE performance. Other reports indicate further significant associations between AQP1 channel and CE phenotypes. The purposes of this systematic review were to examine the extent of the associations between the
AQP1
rs1049305 genotype and CE exercise performance and body fluid loss in long-distance runners and AQP1 channel associations with other CE phenotypes.
Methods
Data sources: A comprehensive review was conducted using PubMed, EMBASE, CINAHL, and Cochrane electronic databases. The search ranged from January 1, 1988, to December 31, 2018. Studies reported in English, French, and Spanish were considered. Eligibility criteria: The criteria for inclusion in the review were (a) case-control study; (b) unequivocal definition of cases and controls; (c) CE was defined as performance in endurance events, laboratory tests, and/or maximal oxygen consumption; (d) exclusion criteria of known causes; (e) genotyping performed by PCR or sequencing; (f) genotype frequencies reported; and (g) no deviation of genotype frequencies from Hardy-Weinberg equilibrium in the control group. Study appraisal: The systematic review included studies examining the
AQP1
gene and AQP1 channel structure and function, associations between the
AQP1
gene sequence variant rs1049305 (C > G) and CE performance, body fluid loss in long-distance runners, and other studies reporting on the
AQP1
gene and channel CE phenotype associations. Synthesis methods: For each selected study, the following data were extracted: authors, year of publication, sample size and number of cases and controls, CE definition, exclusion criteria, inclusion criteria for cases and controls, methods used for genotyping, genotype, allele frequencies and HWE for genotype frequencies in cases and control groups, and method of
AQP1
gene and AQP1 channel analysis.
Results
The initial databases search found 172 pertinent studies. Of those, 46 studies were utilized in the final synthesis of the systematic review. The most relevant findings were (a) the identification of an independent replication of the association between
AQP1
gene sequence variant rs1049305 (C > G) and CE performance; (b) the association of the rs1049305 C-allele with faster CE running performance; (c) in knockout model, using a linear regression analysis of distance run as a function of Aqp1 status (Aqp1-null vs. wild-type mice) and conditions of hypoxia (ambient [O
2
] = 16%), normoxia (21%), and hyperoxia (40%) indicated that the Aqp1 knockout ran less distance than the wild-type mice (
p
< 0.001); (d) in vitro, a reduced
AQP1
expression was associated with the presence of the rs1049305 G-allele; (e) AQP1 null humans led normal lives and were entirely unaware of any physical limitations. However, they could not support fluid homeostasis when exposed to chronic fluid overload. The limited number of studies with “adequate sample sizes” in various racial and ethnic groups precluding to perform proper in-depth statistical analysis.
Conclusions
The
AQP1
gene and AQP1 channel seems to support homeostatic mechanisms, yet to be totally understood, that are auxiliary in achieving an advantage during endurance exercise. AQP1 functions are vital during exercise and have a profound influence on endurance running performance. AQP1s are underappreciated structures that play vital roles in cellular homeostasis at rest and during CE endurance running exercise. The outcome of the present systematic review provide support to the statement of hypotheses and further research endeavors on the likely influence of
AQP1
gene and AQP1 channel on CE performance.
Registration
: The protocol is not registered.</description><identifier>ISSN: 2199-1170</identifier><identifier>EISSN: 2198-9761</identifier><identifier>DOI: 10.1186/s40798-019-0213-0</identifier><identifier>PMID: 31486928</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Analysis ; Aquaporins ; Carbonates ; Database searching ; DNA sequencing ; Genotype & phenotype ; Homeostasis ; Hydraulic measurements ; Internet/Web search services ; Medicine ; Medicine & Public Health ; Nitric oxide ; Nucleotide sequencing ; Online searching ; Running ; Sports Medicine ; Studies ; Systematic Review</subject><ispartof>Sports Medicine - Open, 2019-09, Vol.5 (1), p.40-12, Article 40</ispartof><rights>The Author(s). 2019</rights><rights>COPYRIGHT 2019 Springer</rights><rights>Sports Medicine - Open is a copyright of Springer, (2019). All Rights Reserved. © 2019. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c509t-65cb7e32b78216a47729efb666ca24f545cad4c1bde377c48ebb83a55783fee93</citedby><cites>FETCH-LOGICAL-c509t-65cb7e32b78216a47729efb666ca24f545cad4c1bde377c48ebb83a55783fee93</cites><orcidid>0000-0001-7244-8494</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6728102/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6728102/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,41096,41464,42165,42533,51294,51551,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31486928$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rivera, Miguel A.</creatorcontrib><creatorcontrib>Fahey, Thomas D.</creatorcontrib><title>Association Between aquaporin-1 and Endurance Performance: A Systematic Review</title><title>Sports Medicine - Open</title><addtitle>Sports Med - Open</addtitle><addtitle>Sports Med Open</addtitle><description>Background
There is abundant and mounting information related to the molecular and biological structure and function of the
Aquaporin-1
(
AQP1
) gene and the AQP1-Aquaporin channel. Regulation of water flow across cell membranes is essential for supporting inter- and intracellular fluid balance, which is critical for health and exercise performance. The transmembrane water channel AQP1 is important for cardiorespiratory endurance (CE) because it influences fluid transfers in erythrocytes, endothelial, and pulmonary cells and is vital for transport of ammonium, bicarbonate, carbon dioxide, glycerol, nitric oxide, potassium ion, water, and trans-epithelial and renal water. Very recent publications suggest the association between a DNA sequence variant, rs1049305 (C > G), in the 3′-untranslated region of the
AQP1
gene and CE performance. Other reports indicate further significant associations between AQP1 channel and CE phenotypes. The purposes of this systematic review were to examine the extent of the associations between the
AQP1
rs1049305 genotype and CE exercise performance and body fluid loss in long-distance runners and AQP1 channel associations with other CE phenotypes.
Methods
Data sources: A comprehensive review was conducted using PubMed, EMBASE, CINAHL, and Cochrane electronic databases. The search ranged from January 1, 1988, to December 31, 2018. Studies reported in English, French, and Spanish were considered. Eligibility criteria: The criteria for inclusion in the review were (a) case-control study; (b) unequivocal definition of cases and controls; (c) CE was defined as performance in endurance events, laboratory tests, and/or maximal oxygen consumption; (d) exclusion criteria of known causes; (e) genotyping performed by PCR or sequencing; (f) genotype frequencies reported; and (g) no deviation of genotype frequencies from Hardy-Weinberg equilibrium in the control group. Study appraisal: The systematic review included studies examining the
AQP1
gene and AQP1 channel structure and function, associations between the
AQP1
gene sequence variant rs1049305 (C > G) and CE performance, body fluid loss in long-distance runners, and other studies reporting on the
AQP1
gene and channel CE phenotype associations. Synthesis methods: For each selected study, the following data were extracted: authors, year of publication, sample size and number of cases and controls, CE definition, exclusion criteria, inclusion criteria for cases and controls, methods used for genotyping, genotype, allele frequencies and HWE for genotype frequencies in cases and control groups, and method of
AQP1
gene and AQP1 channel analysis.
Results
The initial databases search found 172 pertinent studies. Of those, 46 studies were utilized in the final synthesis of the systematic review. The most relevant findings were (a) the identification of an independent replication of the association between
AQP1
gene sequence variant rs1049305 (C > G) and CE performance; (b) the association of the rs1049305 C-allele with faster CE running performance; (c) in knockout model, using a linear regression analysis of distance run as a function of Aqp1 status (Aqp1-null vs. wild-type mice) and conditions of hypoxia (ambient [O
2
] = 16%), normoxia (21%), and hyperoxia (40%) indicated that the Aqp1 knockout ran less distance than the wild-type mice (
p
< 0.001); (d) in vitro, a reduced
AQP1
expression was associated with the presence of the rs1049305 G-allele; (e) AQP1 null humans led normal lives and were entirely unaware of any physical limitations. However, they could not support fluid homeostasis when exposed to chronic fluid overload. The limited number of studies with “adequate sample sizes” in various racial and ethnic groups precluding to perform proper in-depth statistical analysis.
Conclusions
The
AQP1
gene and AQP1 channel seems to support homeostatic mechanisms, yet to be totally understood, that are auxiliary in achieving an advantage during endurance exercise. AQP1 functions are vital during exercise and have a profound influence on endurance running performance. AQP1s are underappreciated structures that play vital roles in cellular homeostasis at rest and during CE endurance running exercise. The outcome of the present systematic review provide support to the statement of hypotheses and further research endeavors on the likely influence of
AQP1
gene and AQP1 channel on CE performance.
Registration
: The protocol is not registered.</description><subject>Analysis</subject><subject>Aquaporins</subject><subject>Carbonates</subject><subject>Database searching</subject><subject>DNA sequencing</subject><subject>Genotype & phenotype</subject><subject>Homeostasis</subject><subject>Hydraulic measurements</subject><subject>Internet/Web search services</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Nitric oxide</subject><subject>Nucleotide sequencing</subject><subject>Online searching</subject><subject>Running</subject><subject>Sports Medicine</subject><subject>Studies</subject><subject>Systematic Review</subject><issn>2199-1170</issn><issn>2198-9761</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>BENPR</sourceid><recordid>eNp1UctuFDEQtBCIREs-gAsaifMkfj84IC1RSCJFEAU4Wx5Pz2K0Y2_smUT5e7xMCHBAPrjVXVVddiH0muBjQrQ8KRwro1tMTIspYS1-hg4pqR2jJHn-qzYtIQofoKNSQocF5pwzzF6iA0a4lobqQ_RpXUrywU0hxeYDTPcAsXG3s9ulHGJLGhf75iz2c3bRQ3MNeUh53NfvmnXz5aFMMFayb27gLsD9K_RicNsCR4_3Cn37ePb19KK9-nx-ebq-ar3AZmql8J0CRjulKZGOK0UNDJ2U0jvKB8GFdz33pOuBKeW5hq7TzAmhNBsADFuh94vubu5G6D3EKbut3eUwuvxgkwv230kM3-0m3VmpqCaYVoG3jwI53c5QJvsjzTlWz5ZSzbXm-09doeMFtXFbsCEOqYr5enoYg08RhlD7a2G0kEopVglkIficSskwPFki2O5js0tstsZm9xssrpw3f7_lifE7pAqgC6DUUdxA_uP1_6o_AbL9ozg</recordid><startdate>20190905</startdate><enddate>20190905</enddate><creator>Rivera, Miguel A.</creator><creator>Fahey, Thomas D.</creator><general>Springer International Publishing</general><general>Springer</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IAO</scope><scope>3V.</scope><scope>7RV</scope><scope>7TS</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>KB0</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-7244-8494</orcidid></search><sort><creationdate>20190905</creationdate><title>Association Between aquaporin-1 and Endurance Performance: A Systematic Review</title><author>Rivera, Miguel A. ; Fahey, Thomas D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c509t-65cb7e32b78216a47729efb666ca24f545cad4c1bde377c48ebb83a55783fee93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Analysis</topic><topic>Aquaporins</topic><topic>Carbonates</topic><topic>Database searching</topic><topic>DNA sequencing</topic><topic>Genotype & phenotype</topic><topic>Homeostasis</topic><topic>Hydraulic measurements</topic><topic>Internet/Web search services</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Nitric oxide</topic><topic>Nucleotide sequencing</topic><topic>Online searching</topic><topic>Running</topic><topic>Sports Medicine</topic><topic>Studies</topic><topic>Systematic Review</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rivera, Miguel A.</creatorcontrib><creatorcontrib>Fahey, Thomas D.</creatorcontrib><collection>Springer Nature OA/Free Journals</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale Academic OneFile</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Physical Education Index</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Nursing & Allied Health Premium</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Sports Medicine - Open</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rivera, Miguel A.</au><au>Fahey, Thomas D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association Between aquaporin-1 and Endurance Performance: A Systematic Review</atitle><jtitle>Sports Medicine - Open</jtitle><stitle>Sports Med - Open</stitle><addtitle>Sports Med Open</addtitle><date>2019-09-05</date><risdate>2019</risdate><volume>5</volume><issue>1</issue><spage>40</spage><epage>12</epage><pages>40-12</pages><artnum>40</artnum><issn>2199-1170</issn><eissn>2198-9761</eissn><abstract>Background
There is abundant and mounting information related to the molecular and biological structure and function of the
Aquaporin-1
(
AQP1
) gene and the AQP1-Aquaporin channel. Regulation of water flow across cell membranes is essential for supporting inter- and intracellular fluid balance, which is critical for health and exercise performance. The transmembrane water channel AQP1 is important for cardiorespiratory endurance (CE) because it influences fluid transfers in erythrocytes, endothelial, and pulmonary cells and is vital for transport of ammonium, bicarbonate, carbon dioxide, glycerol, nitric oxide, potassium ion, water, and trans-epithelial and renal water. Very recent publications suggest the association between a DNA sequence variant, rs1049305 (C > G), in the 3′-untranslated region of the
AQP1
gene and CE performance. Other reports indicate further significant associations between AQP1 channel and CE phenotypes. The purposes of this systematic review were to examine the extent of the associations between the
AQP1
rs1049305 genotype and CE exercise performance and body fluid loss in long-distance runners and AQP1 channel associations with other CE phenotypes.
Methods
Data sources: A comprehensive review was conducted using PubMed, EMBASE, CINAHL, and Cochrane electronic databases. The search ranged from January 1, 1988, to December 31, 2018. Studies reported in English, French, and Spanish were considered. Eligibility criteria: The criteria for inclusion in the review were (a) case-control study; (b) unequivocal definition of cases and controls; (c) CE was defined as performance in endurance events, laboratory tests, and/or maximal oxygen consumption; (d) exclusion criteria of known causes; (e) genotyping performed by PCR or sequencing; (f) genotype frequencies reported; and (g) no deviation of genotype frequencies from Hardy-Weinberg equilibrium in the control group. Study appraisal: The systematic review included studies examining the
AQP1
gene and AQP1 channel structure and function, associations between the
AQP1
gene sequence variant rs1049305 (C > G) and CE performance, body fluid loss in long-distance runners, and other studies reporting on the
AQP1
gene and channel CE phenotype associations. Synthesis methods: For each selected study, the following data were extracted: authors, year of publication, sample size and number of cases and controls, CE definition, exclusion criteria, inclusion criteria for cases and controls, methods used for genotyping, genotype, allele frequencies and HWE for genotype frequencies in cases and control groups, and method of
AQP1
gene and AQP1 channel analysis.
Results
The initial databases search found 172 pertinent studies. Of those, 46 studies were utilized in the final synthesis of the systematic review. The most relevant findings were (a) the identification of an independent replication of the association between
AQP1
gene sequence variant rs1049305 (C > G) and CE performance; (b) the association of the rs1049305 C-allele with faster CE running performance; (c) in knockout model, using a linear regression analysis of distance run as a function of Aqp1 status (Aqp1-null vs. wild-type mice) and conditions of hypoxia (ambient [O
2
] = 16%), normoxia (21%), and hyperoxia (40%) indicated that the Aqp1 knockout ran less distance than the wild-type mice (
p
< 0.001); (d) in vitro, a reduced
AQP1
expression was associated with the presence of the rs1049305 G-allele; (e) AQP1 null humans led normal lives and were entirely unaware of any physical limitations. However, they could not support fluid homeostasis when exposed to chronic fluid overload. The limited number of studies with “adequate sample sizes” in various racial and ethnic groups precluding to perform proper in-depth statistical analysis.
Conclusions
The
AQP1
gene and AQP1 channel seems to support homeostatic mechanisms, yet to be totally understood, that are auxiliary in achieving an advantage during endurance exercise. AQP1 functions are vital during exercise and have a profound influence on endurance running performance. AQP1s are underappreciated structures that play vital roles in cellular homeostasis at rest and during CE endurance running exercise. The outcome of the present systematic review provide support to the statement of hypotheses and further research endeavors on the likely influence of
AQP1
gene and AQP1 channel on CE performance.
Registration
: The protocol is not registered.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>31486928</pmid><doi>10.1186/s40798-019-0213-0</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0001-7244-8494</orcidid><oa>free_for_read</oa></addata></record> |
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source | Springer Online Journals Complete; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Springer Nature OA/Free Journals; PubMed Central Open Access |
subjects | Analysis Aquaporins Carbonates Database searching DNA sequencing Genotype & phenotype Homeostasis Hydraulic measurements Internet/Web search services Medicine Medicine & Public Health Nitric oxide Nucleotide sequencing Online searching Running Sports Medicine Studies Systematic Review |
title | Association Between aquaporin-1 and Endurance Performance: A Systematic Review |
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