High-sensitive troponin T, suPAR and Beta-2-microglobulin changes in concentration during hemodialysis

Hemodialysis (HD) patients are at high risk of cardiovascular disease and death. Reliable biomarkers for risk stratification and detection of acute myocardial infarction (AMI) are therefore pivotal. Cardiac troponins (cTn) are the preferred biomarkers for AMI. It remains unclear, if cTn concentratio...

Full description

Saved in:
Bibliographic Details
Published in:Scandinavian journal of clinical and laboratory investigation Vol. 84; no. 5; pp. 362 - 368
Main Authors: Kampmann, Jan D, Hunderup, Michael M, Petersen, Eva R Brix, Andersen, Vivi, Skovsted, Thor A
Format: Journal Article
Language:English
Published: England 01-09-2024
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Abstract Hemodialysis (HD) patients are at high risk of cardiovascular disease and death. Reliable biomarkers for risk stratification and detection of acute myocardial infarction (AMI) are therefore pivotal. Cardiac troponins (cTn) are the preferred biomarkers for AMI. It remains unclear, if cTn concentrations changes as a consequence of HD treatment itself during dialysis. In this study, cTn was compared with soluble urokinase plasminogen activator receptor (suPAR) and Beta-2-microglobulin (B2M). We performed a prospective study including 17 HD patients measuring high-sensitive cardiac troponin t (hs-cTnT), suPAR and B2M before and after a dialysis session and verified the results in a random subgroup of eight patients from the group by repeating their measurements before and after a dialysis session 15 weeks later. Biomarker concentrations after dialysis were adjusted according to hemodilution or concentration according to the hemoglobin concentration. The average hs-cTnT concentration decreased significantly by -9.9% after dialysis (95% CI: -13.6% to -6.2%). The average (paired) difference were - 6.7 ng/L (  = 0.0104) after dialysis comparing 25 HD treatment occasions. SuPAR was not significantly influenced by dialysis. B2M decreased by -58% after HD as an expected result from the molecular size of the biomarker. The hs-cTnT in average decreased by -9.9% after dialysis. This is a diagnostic challenge since the current guidelines suggest a 20% change in hs-cTnT in patients with acute myocardial infarction. Larger prospective studies investigating the different factors influencing hs-cTnT after HD are warranted. Adjusting biomarker concentrations according to hemodilution or concentration using the hemoglobin concentration, should be considered in future studies to determine more exact changes in concentrations of cTnT and other relevant biomarkers.
AbstractList Hemodialysis (HD) patients are at high risk of cardiovascular disease and death. Reliable biomarkers for risk stratification and detection of acute myocardial infarction (AMI) are therefore pivotal. Cardiac troponins (cTn) are the preferred biomarkers for AMI. It remains unclear, if cTn concentrations changes as a consequence of HD treatment itself during dialysis. In this study, cTn was compared with soluble urokinase plasminogen activator receptor (suPAR) and Beta-2-microglobulin (B2M). We performed a prospective study including 17 HD patients measuring high-sensitive cardiac troponin t (hs-cTnT), suPAR and B2M before and after a dialysis session and verified the results in a random subgroup of eight patients from the group by repeating their measurements before and after a dialysis session 15 weeks later. Biomarker concentrations after dialysis were adjusted according to hemodilution or concentration according to the hemoglobin concentration. The average hs-cTnT concentration decreased significantly by -9.9% after dialysis (95% CI: -13.6% to -6.2%). The average (paired) difference were - 6.7 ng/L (p = 0.0104) after dialysis comparing 25 HD treatment occasions. SuPAR was not significantly influenced by dialysis. B2M decreased by -58% after HD as an expected result from the molecular size of the biomarker. The hs-cTnT in average decreased by -9.9% after dialysis. This is a diagnostic challenge since the current guidelines suggest a 20% change in hs-cTnT in patients with acute myocardial infarction. Larger prospective studies investigating the different factors influencing hs-cTnT after HD are warranted. Adjusting biomarker concentrations according to hemodilution or concentration using the hemoglobin concentration, should be considered in future studies to determine more exact changes in concentrations of cTnT and other relevant biomarkers.Hemodialysis (HD) patients are at high risk of cardiovascular disease and death. Reliable biomarkers for risk stratification and detection of acute myocardial infarction (AMI) are therefore pivotal. Cardiac troponins (cTn) are the preferred biomarkers for AMI. It remains unclear, if cTn concentrations changes as a consequence of HD treatment itself during dialysis. In this study, cTn was compared with soluble urokinase plasminogen activator receptor (suPAR) and Beta-2-microglobulin (B2M). We performed a prospective study including 17 HD patients measuring high-sensitive cardiac troponin t (hs-cTnT), suPAR and B2M before and after a dialysis session and verified the results in a random subgroup of eight patients from the group by repeating their measurements before and after a dialysis session 15 weeks later. Biomarker concentrations after dialysis were adjusted according to hemodilution or concentration according to the hemoglobin concentration. The average hs-cTnT concentration decreased significantly by -9.9% after dialysis (95% CI: -13.6% to -6.2%). The average (paired) difference were - 6.7 ng/L (p = 0.0104) after dialysis comparing 25 HD treatment occasions. SuPAR was not significantly influenced by dialysis. B2M decreased by -58% after HD as an expected result from the molecular size of the biomarker. The hs-cTnT in average decreased by -9.9% after dialysis. This is a diagnostic challenge since the current guidelines suggest a 20% change in hs-cTnT in patients with acute myocardial infarction. Larger prospective studies investigating the different factors influencing hs-cTnT after HD are warranted. Adjusting biomarker concentrations according to hemodilution or concentration using the hemoglobin concentration, should be considered in future studies to determine more exact changes in concentrations of cTnT and other relevant biomarkers.
Hemodialysis (HD) patients are at high risk of cardiovascular disease and death. Reliable biomarkers for risk stratification and detection of acute myocardial infarction (AMI) are therefore pivotal. Cardiac troponins (cTn) are the preferred biomarkers for AMI. It remains unclear, if cTn concentrations changes as a consequence of HD treatment itself during dialysis. In this study, cTn was compared with soluble urokinase plasminogen activator receptor (suPAR) and Beta-2-microglobulin (B2M). We performed a prospective study including 17 HD patients measuring high-sensitive cardiac troponin t (hs-cTnT), suPAR and B2M before and after a dialysis session and verified the results in a random subgroup of eight patients from the group by repeating their measurements before and after a dialysis session 15 weeks later. Biomarker concentrations after dialysis were adjusted according to hemodilution or concentration according to the hemoglobin concentration. The average hs-cTnT concentration decreased significantly by -9.9% after dialysis (95% CI: -13.6% to -6.2%). The average (paired) difference were - 6.7 ng/L (  = 0.0104) after dialysis comparing 25 HD treatment occasions. SuPAR was not significantly influenced by dialysis. B2M decreased by -58% after HD as an expected result from the molecular size of the biomarker. The hs-cTnT in average decreased by -9.9% after dialysis. This is a diagnostic challenge since the current guidelines suggest a 20% change in hs-cTnT in patients with acute myocardial infarction. Larger prospective studies investigating the different factors influencing hs-cTnT after HD are warranted. Adjusting biomarker concentrations according to hemodilution or concentration using the hemoglobin concentration, should be considered in future studies to determine more exact changes in concentrations of cTnT and other relevant biomarkers.
Author Andersen, Vivi
Skovsted, Thor A
Kampmann, Jan D
Petersen, Eva R Brix
Hunderup, Michael M
Author_xml – sequence: 1
  givenname: Jan D
  surname: Kampmann
  fullname: Kampmann, Jan D
  organization: Department of Internal Medicine, University Hospital of Southern Denmark, Sønderborg, Denmark
– sequence: 2
  givenname: Michael M
  surname: Hunderup
  fullname: Hunderup, Michael M
  organization: Department of Blood Test, Biochemistry and Immunology, University Hospital of Southern Denmark, Sønderborg, Denmark
– sequence: 3
  givenname: Eva R Brix
  surname: Petersen
  fullname: Petersen, Eva R Brix
  organization: Department of Biochemistry, Lillebaelt Hospital, University Hospital of Southern Denmark, Vejle, Denmark
– sequence: 4
  givenname: Vivi
  surname: Andersen
  fullname: Andersen, Vivi
  organization: Department of Internal Medicine, University Hospital of Southern Denmark, Sønderborg, Denmark
– sequence: 5
  givenname: Thor A
  orcidid: 0000-0003-3147-3030
  surname: Skovsted
  fullname: Skovsted, Thor A
  organization: Department of Blood Test, Biochemistry and Immunology, University Hospital of Southern Denmark, Sønderborg, Denmark
BackLink https://www.ncbi.nlm.nih.gov/pubmed/39180468$$D View this record in MEDLINE/PubMed
BookMark eNo9kN9LwzAQx4NM3A_9E5Q--mDnpUnT5HEOdcJAkflc0iTdIm0ym1bYf2_LNp_uDj7fO-4zRSPnnUHoFsMcA4dHAMLSFJN5AgmdJ0TQTNALNMEpJHHGOBuhycDEAzRG0xC-oZ8Jp1doTATmQBmfoHJlt7s4GBdsa39N1DZ-75110eYhCt3H4jOSTkdPppVxEtdWNX5b-aKrekLtpNuaEA2td8q4tpGt9S7SXWPdNtqZ2msrq0Ow4RpdlrIK5uZUZ-jr5XmzXMXr99e35WIdq4TQNqZCZFAwpQVWGS6JBmCUMabKgmFNOEshzQSXnFNKiTQ6ySgkilNIMdaSkxm6P-7dN_6nM6HNaxuUqSrpjO9CTkD06_qM6NH0iPY_hdCYMt83tpbNIceQD4rzs-J8UJyfFPe5u9OJrqiN_k-dnZI_R5d3zQ
Cites_doi 10.1111/j.1440-1797.2012.01625.x
10.1111/sdi.13178
10.3349/ymj.2011.52.4.595
10.1016/j.amjcard.2017.08.026
10.1016/j.ekir.2018.05.004
10.3390/diagnostics12020276
10.1038/ki.2009.541
10.1016/j.jacc.2018.08.1038
10.1373/clinchem.2013.216978
10.1155/2009/504294
10.1038/srep41350
10.1161/CIR.0000000000000617
10.1093/ndt/gfi125
10.1159/000524965
10.1080/00365513.2020.1741674
10.1373/clinchem.2016.261644
10.1373/clinchem.2007.095679
10.1016/j.jacc.2019.08.1017
10.1111/hdi.12514
10.1053/ajkd.2002.34913
10.1038/sj.ki.5000048
10.1136/hrt.2005.071282
10.5812/numonthly.23563
10.5301/ijao.5000387
10.1093/ckj/sfs122
10.1111/j.1755-6686.2010.00171.x
10.1046/j.1525-139x.2002.00083.x
10.1016/s0009-9120(02)00328-4
10.1161/CIRCULATIONAHA.106.683722
10.1053/j.ajkd.2016.12.004
10.1038/ki.2014.197
10.1016/S0140-6736(16)30448-2
10.1136/openhrt-2014-000108
10.1080/00365513.2016.1230886
10.5301/jn.5000169
10.1093/ndt/gfz189
10.1016/j.clinbiochem.2019.05.010
10.1515/cclm-2021-5004
ContentType Journal Article
DBID CGR
CUY
CVF
ECM
EIF
NPM
AAYXX
CITATION
7X8
DOI 10.1080/00365513.2024.2394794
DatabaseName Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
CrossRef
MEDLINE - Academic
DatabaseTitle MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
CrossRef
MEDLINE - Academic
DatabaseTitleList MEDLINE - Academic
MEDLINE
Database_xml – sequence: 1
  dbid: ECM
  name: MEDLINE
  url: https://search.ebscohost.com/login.aspx?direct=true&db=cmedm&site=ehost-live
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 1502-7686
EndPage 368
ExternalDocumentID 10_1080_00365513_2024_2394794
39180468
Genre Journal Article
GroupedDBID ---
-~X
.55
.GJ
00X
03L
0BK
0R~
123
34G
36B
39C
3O-
4.4
53G
5RE
5VS
AALIY
AALUX
AAMIU
AAORF
AAPUL
AAPXX
AAQQT
AAQRR
AAWTL
ABBKH
ABDBF
ABEIZ
ABJNI
ABLIJ
ABLJU
ABLKL
ABOCM
ABUPF
ABWCV
ABXYU
ABZEW
ACENM
ACGEJ
ACGFS
ACIEZ
ACKZS
ADCVX
ADFOM
ADFZZ
ADRBQ
ADXPE
AECIN
AEIIZ
AENEX
AEOZL
AFFNX
AFKVX
AFLEI
AGDLA
AGFJD
AGRBW
AGYJP
AIJEM
AIRBT
AJVHN
AJWEG
AKBVH
ALMA_UNASSIGNED_HOLDINGS
ALQZU
ALYBC
AMDAE
AWYRJ
BABNJ
BLEHA
BOHLJ
BRMBE
CAG
CCCUG
CGR
COF
CS3
CUY
CVF
CYYVM
CZDIS
DKSSO
DRXRE
DU5
DWTOO
EAP
EAS
EBB
EBC
EBD
EBS
EBX
ECM
EHN
EIF
EJD
EMB
EMK
EMOBN
EPL
EPT
ESX
F5P
H13
HZ~
JENTW
KRBQP
KSSTO
KWAYT
KYCEM
L7B
LJTGL
M44
M4Z
NPM
NUSFT
O9-
OVD
P2P
QQXMO
Q~Q
RNANH
RVRKI
SV3
TBQAZ
TDBHL
TEORI
TERGH
TFDNU
TFL
TFW
TUROJ
TUS
UEQFS
UHWXJ
V1S
WH7
X7M
ZGI
ZXP
~1N
AAYXX
CITATION
7X8
ID FETCH-LOGICAL-c234t-49970b6cd91c71f3d0064666cfb61d386505798a884443aed27402c840511da83
ISSN 0036-5513
1502-7686
IngestDate Sat Oct 26 03:57:58 EDT 2024
Wed Nov 20 13:22:14 EST 2024
Sat Nov 02 12:00:51 EDT 2024
IsDoiOpenAccess false
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 5
Keywords soluble urokinase plasminogen activator receptor
cardiovascular disease
end-stage kidney disease
high-sensitive cardiac troponin t
Hemodialysis
acute myocardial infarction
Language English
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-c234t-49970b6cd91c71f3d0064666cfb61d386505798a884443aed27402c840511da83
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ORCID 0000-0003-3147-3030
OpenAccessLink https://www.tandfonline.com/doi/pdf/10.1080/00365513.2024.2394794?needAccess=true
PMID 39180468
PQID 3096664029
PQPubID 23479
PageCount 7
ParticipantIDs proquest_miscellaneous_3096664029
crossref_primary_10_1080_00365513_2024_2394794
pubmed_primary_39180468
PublicationCentury 2000
PublicationDate 2024-Sep
PublicationDateYYYYMMDD 2024-09-01
PublicationDate_xml – month: 09
  year: 2024
  text: 2024-Sep
PublicationDecade 2020
PublicationPlace England
PublicationPlace_xml – name: England
PublicationTitle Scandinavian journal of clinical and laboratory investigation
PublicationTitleAlternate Scand J Clin Lab Invest
PublicationYear 2024
References e_1_3_3_30_1
e_1_3_3_18_1
e_1_3_3_17_1
e_1_3_3_39_1
e_1_3_3_19_1
e_1_3_3_14_1
e_1_3_3_37_1
e_1_3_3_13_1
e_1_3_3_38_1
e_1_3_3_16_1
e_1_3_3_35_1
e_1_3_3_15_1
e_1_3_3_36_1
e_1_3_3_10_1
e_1_3_3_34_1
e_1_3_3_12_1
e_1_3_3_31_1
e_1_3_3_11_1
e_1_3_3_32_1
e_1_3_3_40_1
e_1_3_3_41_1
Saran R (e_1_3_3_4_1) 2017; 69
The Clinical & Laboratory Standards Institute (CLSI) (e_1_3_3_33_1) 2017
e_1_3_3_7_1
e_1_3_3_6_1
e_1_3_3_9_1
e_1_3_3_8_1
e_1_3_3_29_1
e_1_3_3_28_1
e_1_3_3_25_1
e_1_3_3_24_1
e_1_3_3_27_1
e_1_3_3_26_1
e_1_3_3_3_1
e_1_3_3_21_1
e_1_3_3_2_1
e_1_3_3_20_1
e_1_3_3_5_1
e_1_3_3_23_1
e_1_3_3_42_1
e_1_3_3_22_1
References_xml – ident: e_1_3_3_39_1
  doi: 10.1111/j.1440-1797.2012.01625.x
– ident: e_1_3_3_12_1
  doi: 10.1111/sdi.13178
– ident: e_1_3_3_25_1
  doi: 10.3349/ymj.2011.52.4.595
– ident: e_1_3_3_11_1
  doi: 10.1016/j.amjcard.2017.08.026
– ident: e_1_3_3_21_1
  doi: 10.1016/j.ekir.2018.05.004
– ident: e_1_3_3_27_1
  doi: 10.3390/diagnostics12020276
– ident: e_1_3_3_29_1
  doi: 10.1038/ki.2009.541
– ident: e_1_3_3_5_1
  doi: 10.1016/j.jacc.2018.08.1038
– ident: e_1_3_3_8_1
  doi: 10.1373/clinchem.2013.216978
– ident: e_1_3_3_31_1
  doi: 10.1155/2009/504294
– ident: e_1_3_3_26_1
  doi: 10.1038/srep41350
– volume-title: Collection of diagnostic venous blood specimens
  year: 2017
  ident: e_1_3_3_33_1
  contributor:
    fullname: The Clinical & Laboratory Standards Institute (CLSI)
– ident: e_1_3_3_7_1
  doi: 10.1161/CIR.0000000000000617
– ident: e_1_3_3_14_1
  doi: 10.1093/ndt/gfi125
– ident: e_1_3_3_17_1
  doi: 10.1159/000524965
– ident: e_1_3_3_36_1
  doi: 10.1080/00365513.2020.1741674
– ident: e_1_3_3_32_1
  doi: 10.1373/clinchem.2016.261644
– ident: e_1_3_3_6_1
  doi: 10.1373/clinchem.2007.095679
– ident: e_1_3_3_10_1
  doi: 10.1016/j.jacc.2019.08.1017
– ident: e_1_3_3_42_1
  doi: 10.1111/hdi.12514
– ident: e_1_3_3_41_1
  doi: 10.1053/ajkd.2002.34913
– ident: e_1_3_3_22_1
  doi: 10.1038/sj.ki.5000048
– ident: e_1_3_3_9_1
  doi: 10.1136/hrt.2005.071282
– ident: e_1_3_3_23_1
  doi: 10.5812/numonthly.23563
– ident: e_1_3_3_15_1
  doi: 10.5301/ijao.5000387
– ident: e_1_3_3_40_1
  doi: 10.1093/ckj/sfs122
– ident: e_1_3_3_3_1
  doi: 10.1111/j.1755-6686.2010.00171.x
– ident: e_1_3_3_18_1
  doi: 10.1046/j.1525-139x.2002.00083.x
– ident: e_1_3_3_13_1
  doi: 10.1016/s0009-9120(02)00328-4
– ident: e_1_3_3_24_1
  doi: 10.1161/CIRCULATIONAHA.106.683722
– volume: 69
  start-page: ):S1
  issue: 3
  year: 2017
  ident: e_1_3_3_4_1
  article-title: US Renal Data System 2016 Annual Data Report: epidemiology of kidney disease in the United States
  publication-title: Am J Kidney Dis
  doi: 10.1053/j.ajkd.2016.12.004
  contributor:
    fullname: Saran R
– ident: e_1_3_3_20_1
  doi: 10.1038/ki.2014.197
– ident: e_1_3_3_2_1
  doi: 10.1016/S0140-6736(16)30448-2
– ident: e_1_3_3_34_1
– ident: e_1_3_3_16_1
  doi: 10.1136/openhrt-2014-000108
– ident: e_1_3_3_38_1
  doi: 10.1080/00365513.2016.1230886
– ident: e_1_3_3_19_1
  doi: 10.5301/jn.5000169
– ident: e_1_3_3_37_1
– ident: e_1_3_3_28_1
  doi: 10.1093/ndt/gfz189
– ident: e_1_3_3_30_1
  doi: 10.1016/j.clinbiochem.2019.05.010
– ident: e_1_3_3_35_1
  doi: 10.1515/cclm-2021-5004
SSID ssj0003384
Score 2.4224632
Snippet Hemodialysis (HD) patients are at high risk of cardiovascular disease and death. Reliable biomarkers for risk stratification and detection of acute myocardial...
SourceID proquest
crossref
pubmed
SourceType Aggregation Database
Index Database
StartPage 362
SubjectTerms Aged
beta 2-Microglobulin - blood
Biomarkers - blood
Female
Humans
Male
Middle Aged
Myocardial Infarction - blood
Myocardial Infarction - diagnosis
Prospective Studies
Receptors, Urokinase Plasminogen Activator - blood
Renal Dialysis
Troponin T - blood
Title High-sensitive troponin T, suPAR and Beta-2-microglobulin changes in concentration during hemodialysis
URI https://www.ncbi.nlm.nih.gov/pubmed/39180468
https://www.proquest.com/docview/3096664029
Volume 84
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1La9wwEBabBEovoe9umhQVemu92JYsy8dt4pBDsi2JU3IzsmXTPaw3ZNdLfn5nZPmxdAvpoRchZCybmY-RRvpmhpDPsAf2ApXnjoqYcLjQmQMdDQ0LpeCKCZNd_-ImnN3Js5jHo1FbW7Af-6-ahjHQNUbO_oO2u0lhAPqgc2hB69A-Se9I3HBWSEs3pKA1VkHABKoJCnNV_5hem_uCb8VaOb6zQD4eJgVpCOkm1MAwZHMMZ6xsTt02mPFXsVhioAlmMRnuam9yExyjNnN7rG-3uF3YJX7Rwg3v9Od9co8BC0AtMBKiiRWBec56xGEATn0_YPn3Z7iGX9yeIm3Ul2s87njsDzd09_TnfDMfnnH4vCNxdWYZ7DY4RjZp9o4xa8ubcnMWs8HAMLPG5v-xYLQMS8Bk4LEJfnyC1eLDpvTydoLu2ff0_PbyMk3iu2SPHPhg28C0HkxP49lVt_yDz2-oDO3vtWFjmNB912e2N0R_8XLMbid5QQ6tm0KnDb5eklFRvSLPriwR4zUpt2FGW5jR5Cs1IKOgcroLZNSCjGJ3CDLagIwOQfaG3J7HyemFY0t2OLnP-NoB_zl0M5HryMtDr2Qat7zgIedlJjyN9WUx-FkqKTnnTBXaD7nr5xLcBs_TSrK3ZL9aVsV7QjNWahnAGxHPeMCUUm6keeGXsMQUXLljMmnllt43mVlSr094awSdoqBTK-gx-dRKNwUbihdjqiqW9Spl4McLAT8Sjcm7RuzdlCzypMuFPHrC2x_I8x69x2R__VAXJ2RvpeuPFiW_AfQblhw
link.rule.ids 315,782,786,27933,27934
linkProvider Taylor & Francis
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=High-sensitive+troponin+T%2C+suPAR+and+Beta-2-microglobulin+changes+in+concentration+during+hemodialysis&rft.jtitle=Scandinavian+journal+of+clinical+and+laboratory+investigation&rft.au=Kampmann%2C+Jan+D&rft.au=Hunderup%2C+Michael+M&rft.au=Petersen%2C+Eva+R+Brix&rft.au=Andersen%2C+Vivi&rft.date=2024-09-01&rft.issn=1502-7686&rft.eissn=1502-7686&rft.volume=84&rft.issue=5&rft.spage=362&rft_id=info:doi/10.1080%2F00365513.2024.2394794&rft.externalDBID=NO_FULL_TEXT
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0036-5513&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0036-5513&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0036-5513&client=summon