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The interaction between glycemic index, glycemic load, and the genetic variant ADIPOQ T45G (rs2241766) in the risk of colorectal cancer: a case–control study in a Korean population
Purpose The glycemic index (GI), glycemic load (GL), and adiponectin level contribute to glycemic response and insulin sensitivity in the body. Studies have shown that tumor development is related to glycemic disorders; however, the results are contradictory. We aimed to investigate the association...
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Published in: | European journal of nutrition 2022-08, Vol.61 (5), p.2601-2614 |
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container_end_page | 2614 |
container_issue | 5 |
container_start_page | 2601 |
container_title | European journal of nutrition |
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creator | Lu, Y-Thanh Gunathilake, Madhawa Lee, Jeonghee Oh, Jae Hwan Chang, Hee Jin Sohn, Dae Kyung Shin, Aesun Kim, Jeongseon |
description | Purpose
The glycemic index (GI), glycemic load (GL), and adiponectin level contribute to glycemic response and insulin sensitivity in the body. Studies have shown that tumor development is related to glycemic disorders; however, the results are contradictory. We aimed to investigate the association of GI and GL with colorectal cancer (CRC) risk in a Korean population and their possible interactions with the genetic variant
ADIPOQ
T45G.
Methods and results
A case–control study including 2096 participants with 695 CRC cases was conducted. The results showed that diets with high GI or GL were significantly associated with an increased risk of CRC [odds ratio (OR) = 5.44, 95% confidence interval (CI) 3.85–7.68; OR = 4.43, 95% CI 3.18–6.15, respectively; all
p
-trends |
doi_str_mv | 10.1007/s00394-022-02845-8 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2636148892</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2688768364</sourcerecordid><originalsourceid>FETCH-LOGICAL-c375t-5d227e097ca1d1c1e2945a05a00fa0b517eb9e6e2a716f1e8ffbb8a1c114c2623</originalsourceid><addsrcrecordid>eNp9kc1u1DAUhS0EoqXwAiyQJTZFasD_cdhVBUpFpYI0rKMb52ZIydiD7QCz4x14Fx6IJ8HTKa3EAsmWr-3vHF_5EPKYs-ecsfpFYkw2qmJClGmVruwdss-VNJURXN-9qVm9Rx6kdMkYE9Lw-2RPaqGk1nKf_Fp8Qjr6jBFcHoOnHeZviJ4up43D1ejKZY_fj273U4D-iILvaS7SJXrM5fQrxBF8psevzt5ffKALpU_pYUxCKF4b86y4XOFxTJ9pGKgLU4joMkzUgXcYX1IoVcLfP3664HMME0157jdbIdB3BQZP12E9T7Bt8yG5N8CU8NH1ekA-vnm9OHlbnV-cnp0cn1dO1jpXuheiRtbUDnjPHUfRKA2sDDYA6zSvsWvQoICam4GjHYaus1BIrpwwQh6Qw53vOoYvM6bcrsbkcJrAY5hTK0z5UGVts0Wf_oNehjn60l2hrK2NlUYVSuwoF0NKEYd2HccVxE3LWbtNtd2l2pZU26tUW1tET66t526F_Y3kb4wFkDsglSu_xHj79n9s_wDjf62h</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2688768364</pqid></control><display><type>article</type><title>The interaction between glycemic index, glycemic load, and the genetic variant ADIPOQ T45G (rs2241766) in the risk of colorectal cancer: a case–control study in a Korean population</title><source>Springer Link</source><source>SPORTDiscus with Full Text</source><creator>Lu, Y-Thanh ; Gunathilake, Madhawa ; Lee, Jeonghee ; Oh, Jae Hwan ; Chang, Hee Jin ; Sohn, Dae Kyung ; Shin, Aesun ; Kim, Jeongseon</creator><creatorcontrib>Lu, Y-Thanh ; Gunathilake, Madhawa ; Lee, Jeonghee ; Oh, Jae Hwan ; Chang, Hee Jin ; Sohn, Dae Kyung ; Shin, Aesun ; Kim, Jeongseon</creatorcontrib><description>Purpose
The glycemic index (GI), glycemic load (GL), and adiponectin level contribute to glycemic response and insulin sensitivity in the body. Studies have shown that tumor development is related to glycemic disorders; however, the results are contradictory. We aimed to investigate the association of GI and GL with colorectal cancer (CRC) risk in a Korean population and their possible interactions with the genetic variant
ADIPOQ
T45G.
Methods and results
A case–control study including 2096 participants with 695 CRC cases was conducted. The results showed that diets with high GI or GL were significantly associated with an increased risk of CRC [odds ratio (OR) = 5.44, 95% confidence interval (CI) 3.85–7.68; OR = 4.43, 95% CI 3.18–6.15, respectively; all
p
-trends < 0.001]. Moreover, even with a low-GI and low-GL diet, G/G genotype carriers may have 2.93-fold and 3.77-fold higher risk of rectal cancer compared to carriers of other genotypes (T/T + T/G), (OR = 2.93, 95% CI 1.01–8.59,
p
-interaction = 0.011 for GI; OR = 3.77, 95% CI 1.46–9.77,
p
-interaction = 0.025 for GL).
Conclusions
Overall, our study suggests positive associations of GI and GL with CRC risk. Moreover, the associations of GI and GL with rectal cancer risk could be modified by
ADIPOQ
T45G in a Korean population. Further studies with larger sample sizes are needed to confirm our findings.</description><identifier>ISSN: 1436-6207</identifier><identifier>EISSN: 1436-6215</identifier><identifier>DOI: 10.1007/s00394-022-02845-8</identifier><identifier>PMID: 35243553</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Adiponectin ; Adiponectin - genetics ; Blood Glucose ; Cancer ; Case-Control Studies ; Chemistry ; Chemistry and Materials Science ; Colorectal cancer ; Colorectal carcinoma ; Diet ; Dietary Carbohydrates ; Genetic diversity ; Genotype & phenotype ; Genotypes ; Glycemic Index ; Glycemic Load ; Health risks ; Humans ; Insulin ; Mutation ; Nutrient deficiency ; Nutrition ; Original Contribution ; Population studies ; Rectal Neoplasms ; Rectum ; Republic of Korea - epidemiology ; Risk Factors ; Tumors</subject><ispartof>European journal of nutrition, 2022-08, Vol.61 (5), p.2601-2614</ispartof><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany 2022</rights><rights>2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany.</rights><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany 2022.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-5d227e097ca1d1c1e2945a05a00fa0b517eb9e6e2a716f1e8ffbb8a1c114c2623</citedby><cites>FETCH-LOGICAL-c375t-5d227e097ca1d1c1e2945a05a00fa0b517eb9e6e2a716f1e8ffbb8a1c114c2623</cites><orcidid>0000-0002-0889-2686</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35243553$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lu, Y-Thanh</creatorcontrib><creatorcontrib>Gunathilake, Madhawa</creatorcontrib><creatorcontrib>Lee, Jeonghee</creatorcontrib><creatorcontrib>Oh, Jae Hwan</creatorcontrib><creatorcontrib>Chang, Hee Jin</creatorcontrib><creatorcontrib>Sohn, Dae Kyung</creatorcontrib><creatorcontrib>Shin, Aesun</creatorcontrib><creatorcontrib>Kim, Jeongseon</creatorcontrib><title>The interaction between glycemic index, glycemic load, and the genetic variant ADIPOQ T45G (rs2241766) in the risk of colorectal cancer: a case–control study in a Korean population</title><title>European journal of nutrition</title><addtitle>Eur J Nutr</addtitle><addtitle>Eur J Nutr</addtitle><description>Purpose
The glycemic index (GI), glycemic load (GL), and adiponectin level contribute to glycemic response and insulin sensitivity in the body. Studies have shown that tumor development is related to glycemic disorders; however, the results are contradictory. We aimed to investigate the association of GI and GL with colorectal cancer (CRC) risk in a Korean population and their possible interactions with the genetic variant
ADIPOQ
T45G.
Methods and results
A case–control study including 2096 participants with 695 CRC cases was conducted. The results showed that diets with high GI or GL were significantly associated with an increased risk of CRC [odds ratio (OR) = 5.44, 95% confidence interval (CI) 3.85–7.68; OR = 4.43, 95% CI 3.18–6.15, respectively; all
p
-trends < 0.001]. Moreover, even with a low-GI and low-GL diet, G/G genotype carriers may have 2.93-fold and 3.77-fold higher risk of rectal cancer compared to carriers of other genotypes (T/T + T/G), (OR = 2.93, 95% CI 1.01–8.59,
p
-interaction = 0.011 for GI; OR = 3.77, 95% CI 1.46–9.77,
p
-interaction = 0.025 for GL).
Conclusions
Overall, our study suggests positive associations of GI and GL with CRC risk. Moreover, the associations of GI and GL with rectal cancer risk could be modified by
ADIPOQ
T45G in a Korean population. Further studies with larger sample sizes are needed to confirm our findings.</description><subject>Adiponectin</subject><subject>Adiponectin - genetics</subject><subject>Blood Glucose</subject><subject>Cancer</subject><subject>Case-Control Studies</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Colorectal cancer</subject><subject>Colorectal carcinoma</subject><subject>Diet</subject><subject>Dietary Carbohydrates</subject><subject>Genetic diversity</subject><subject>Genotype & phenotype</subject><subject>Genotypes</subject><subject>Glycemic Index</subject><subject>Glycemic Load</subject><subject>Health risks</subject><subject>Humans</subject><subject>Insulin</subject><subject>Mutation</subject><subject>Nutrient deficiency</subject><subject>Nutrition</subject><subject>Original Contribution</subject><subject>Population studies</subject><subject>Rectal Neoplasms</subject><subject>Rectum</subject><subject>Republic of Korea - epidemiology</subject><subject>Risk Factors</subject><subject>Tumors</subject><issn>1436-6207</issn><issn>1436-6215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9kc1u1DAUhS0EoqXwAiyQJTZFasD_cdhVBUpFpYI0rKMb52ZIydiD7QCz4x14Fx6IJ8HTKa3EAsmWr-3vHF_5EPKYs-ecsfpFYkw2qmJClGmVruwdss-VNJURXN-9qVm9Rx6kdMkYE9Lw-2RPaqGk1nKf_Fp8Qjr6jBFcHoOnHeZviJ4up43D1ejKZY_fj273U4D-iILvaS7SJXrM5fQrxBF8psevzt5ffKALpU_pYUxCKF4b86y4XOFxTJ9pGKgLU4joMkzUgXcYX1IoVcLfP3664HMME0157jdbIdB3BQZP12E9T7Bt8yG5N8CU8NH1ekA-vnm9OHlbnV-cnp0cn1dO1jpXuheiRtbUDnjPHUfRKA2sDDYA6zSvsWvQoICam4GjHYaus1BIrpwwQh6Qw53vOoYvM6bcrsbkcJrAY5hTK0z5UGVts0Wf_oNehjn60l2hrK2NlUYVSuwoF0NKEYd2HccVxE3LWbtNtd2l2pZU26tUW1tET66t526F_Y3kb4wFkDsglSu_xHj79n9s_wDjf62h</recordid><startdate>20220801</startdate><enddate>20220801</enddate><creator>Lu, Y-Thanh</creator><creator>Gunathilake, Madhawa</creator><creator>Lee, Jeonghee</creator><creator>Oh, Jae Hwan</creator><creator>Chang, Hee Jin</creator><creator>Sohn, Dae Kyung</creator><creator>Shin, Aesun</creator><creator>Kim, Jeongseon</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</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>3V.</scope><scope>7QP</scope><scope>7RQ</scope><scope>7RV</scope><scope>7TS</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</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>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-0889-2686</orcidid></search><sort><creationdate>20220801</creationdate><title>The interaction between glycemic index, glycemic load, and the genetic variant ADIPOQ T45G (rs2241766) in the risk of colorectal cancer: a case–control study in a Korean population</title><author>Lu, Y-Thanh ; Gunathilake, Madhawa ; Lee, Jeonghee ; Oh, Jae Hwan ; Chang, Hee Jin ; Sohn, Dae Kyung ; Shin, Aesun ; Kim, Jeongseon</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-5d227e097ca1d1c1e2945a05a00fa0b517eb9e6e2a716f1e8ffbb8a1c114c2623</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Adiponectin</topic><topic>Adiponectin - genetics</topic><topic>Blood Glucose</topic><topic>Cancer</topic><topic>Case-Control Studies</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Colorectal cancer</topic><topic>Colorectal carcinoma</topic><topic>Diet</topic><topic>Dietary Carbohydrates</topic><topic>Genetic diversity</topic><topic>Genotype & phenotype</topic><topic>Genotypes</topic><topic>Glycemic Index</topic><topic>Glycemic Load</topic><topic>Health risks</topic><topic>Humans</topic><topic>Insulin</topic><topic>Mutation</topic><topic>Nutrient deficiency</topic><topic>Nutrition</topic><topic>Original Contribution</topic><topic>Population studies</topic><topic>Rectal Neoplasms</topic><topic>Rectum</topic><topic>Republic of Korea - epidemiology</topic><topic>Risk Factors</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lu, Y-Thanh</creatorcontrib><creatorcontrib>Gunathilake, Madhawa</creatorcontrib><creatorcontrib>Lee, Jeonghee</creatorcontrib><creatorcontrib>Oh, Jae Hwan</creatorcontrib><creatorcontrib>Chang, Hee Jin</creatorcontrib><creatorcontrib>Sohn, Dae Kyung</creatorcontrib><creatorcontrib>Shin, Aesun</creatorcontrib><creatorcontrib>Kim, Jeongseon</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Career & Technical Education Database</collection><collection>Proquest Nursing & Allied Health Source</collection><collection>Physical Education Index</collection><collection>Health & Medical Complete (ProQuest Database)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest Public Health Database</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)</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</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>Consumer Health Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest Central (New)</collection><collection>ProQuest One Academic (New)</collection><collection>ProQuest Health & Medical Research Collection</collection><collection>ProQuest One Academic Middle East (New)</collection><collection>ProQuest One Health & Nursing</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>MEDLINE - Academic</collection><jtitle>European journal of nutrition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lu, Y-Thanh</au><au>Gunathilake, Madhawa</au><au>Lee, Jeonghee</au><au>Oh, Jae Hwan</au><au>Chang, Hee Jin</au><au>Sohn, Dae Kyung</au><au>Shin, Aesun</au><au>Kim, Jeongseon</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The interaction between glycemic index, glycemic load, and the genetic variant ADIPOQ T45G (rs2241766) in the risk of colorectal cancer: a case–control study in a Korean population</atitle><jtitle>European journal of nutrition</jtitle><stitle>Eur J Nutr</stitle><addtitle>Eur J Nutr</addtitle><date>2022-08-01</date><risdate>2022</risdate><volume>61</volume><issue>5</issue><spage>2601</spage><epage>2614</epage><pages>2601-2614</pages><issn>1436-6207</issn><eissn>1436-6215</eissn><abstract>Purpose
The glycemic index (GI), glycemic load (GL), and adiponectin level contribute to glycemic response and insulin sensitivity in the body. Studies have shown that tumor development is related to glycemic disorders; however, the results are contradictory. We aimed to investigate the association of GI and GL with colorectal cancer (CRC) risk in a Korean population and their possible interactions with the genetic variant
ADIPOQ
T45G.
Methods and results
A case–control study including 2096 participants with 695 CRC cases was conducted. The results showed that diets with high GI or GL were significantly associated with an increased risk of CRC [odds ratio (OR) = 5.44, 95% confidence interval (CI) 3.85–7.68; OR = 4.43, 95% CI 3.18–6.15, respectively; all
p
-trends < 0.001]. Moreover, even with a low-GI and low-GL diet, G/G genotype carriers may have 2.93-fold and 3.77-fold higher risk of rectal cancer compared to carriers of other genotypes (T/T + T/G), (OR = 2.93, 95% CI 1.01–8.59,
p
-interaction = 0.011 for GI; OR = 3.77, 95% CI 1.46–9.77,
p
-interaction = 0.025 for GL).
Conclusions
Overall, our study suggests positive associations of GI and GL with CRC risk. Moreover, the associations of GI and GL with rectal cancer risk could be modified by
ADIPOQ
T45G in a Korean population. Further studies with larger sample sizes are needed to confirm our findings.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>35243553</pmid><doi>10.1007/s00394-022-02845-8</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0002-0889-2686</orcidid></addata></record> |
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source | Springer Link; SPORTDiscus with Full Text |
subjects | Adiponectin Adiponectin - genetics Blood Glucose Cancer Case-Control Studies Chemistry Chemistry and Materials Science Colorectal cancer Colorectal carcinoma Diet Dietary Carbohydrates Genetic diversity Genotype & phenotype Genotypes Glycemic Index Glycemic Load Health risks Humans Insulin Mutation Nutrient deficiency Nutrition Original Contribution Population studies Rectal Neoplasms Rectum Republic of Korea - epidemiology Risk Factors Tumors |
title | The interaction between glycemic index, glycemic load, and the genetic variant ADIPOQ T45G (rs2241766) in the risk of colorectal cancer: a case–control study in a Korean population |
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