Lipidomic signatures of post-hepatectomy liver failure using porcine hepatectomy models.

Biomarkers lipidomics liver failure liver regeneration

Journal

Annals of translational medicine
ISSN: 2305-5839
Titre abrégé: Ann Transl Med
Pays: China
ID NLM: 101617978

Informations de publication

Date de publication:
Nov 2020
Historique:
entrez: 14 12 2020
pubmed: 15 12 2020
medline: 15 12 2020
Statut: ppublish

Résumé

Clinical diagnosis of post-hepatectomy liver failure (PHLF) can only be made on or after the 5th postoperative day. Biomarker for early diagnosis is considered as a critical unmet need. Twenty domestic female crossbreed (Yorkshire-landrace and duroc) pigs underwent sham operation (n=6), 70% (n=7) and 90% (n=7) partial hepatectomy (PH). A comprehensive lipidomic analysis was conducted using sera collected at pre-operation (PO), 14, 30, and 48 h after PH using nanoflow ultrahigh performance liquid chromatography-electrospray ionization-tandem mass spectrometry. Of the 184 quantified lipids, 14 lipids showed significant differences between the two resection groups starting at 30 h after surgery. Four phosphatidylcholine (PC) plasmalogen species (P-16:0/16:0, P-18:0/18:2, P-18:0/20:4, and P-18:0/22:6) and PC 32:2 significantly increased in the 90% PH group while these returned to PO level after 30 h in the 70% PH group, presumably implying the failure markers. In contrast, eight triacylglycerol (TG) species (40:0, 42:1, 42:0, 44:1, 44:2, 46:1, 46:2, and 48:3) and sphingomyelin d18:1/20:0 showed an opposite trend, wherein they significantly decreased in the 90% PH group while these in the 70% PH group were abruptly increased until 30 h but returned to near PO levels at 48 h, implying the recovery markers. Same trends could also be observed in the level of whole lipid classes of PC plasmalogens and TGs, in addition to selected individual lipid species. Characteristic lipidomic signatures of PHLF could be identified using large animal models. These candidates have a potential to serve as a tool for early diagnosis and may open new paths to the study to overcome PHLF.

Sections du résumé

BACKGROUND BACKGROUND
Clinical diagnosis of post-hepatectomy liver failure (PHLF) can only be made on or after the 5th postoperative day. Biomarker for early diagnosis is considered as a critical unmet need.
METHODS METHODS
Twenty domestic female crossbreed (Yorkshire-landrace and duroc) pigs underwent sham operation (n=6), 70% (n=7) and 90% (n=7) partial hepatectomy (PH). A comprehensive lipidomic analysis was conducted using sera collected at pre-operation (PO), 14, 30, and 48 h after PH using nanoflow ultrahigh performance liquid chromatography-electrospray ionization-tandem mass spectrometry.
RESULTS RESULTS
Of the 184 quantified lipids, 14 lipids showed significant differences between the two resection groups starting at 30 h after surgery. Four phosphatidylcholine (PC) plasmalogen species (P-16:0/16:0, P-18:0/18:2, P-18:0/20:4, and P-18:0/22:6) and PC 32:2 significantly increased in the 90% PH group while these returned to PO level after 30 h in the 70% PH group, presumably implying the failure markers. In contrast, eight triacylglycerol (TG) species (40:0, 42:1, 42:0, 44:1, 44:2, 46:1, 46:2, and 48:3) and sphingomyelin d18:1/20:0 showed an opposite trend, wherein they significantly decreased in the 90% PH group while these in the 70% PH group were abruptly increased until 30 h but returned to near PO levels at 48 h, implying the recovery markers. Same trends could also be observed in the level of whole lipid classes of PC plasmalogens and TGs, in addition to selected individual lipid species.
CONCLUSIONS CONCLUSIONS
Characteristic lipidomic signatures of PHLF could be identified using large animal models. These candidates have a potential to serve as a tool for early diagnosis and may open new paths to the study to overcome PHLF.

Identifiants

pubmed: 33313108
doi: 10.21037/atm-20-3596
pii: atm-08-21-1363
pmc: PMC7723583
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1363

Informations de copyright

2020 Annals of Translational Medicine. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/atm-20-3596). DSK reports grants from Ministry of Science and ICT through the National Research Foundation (NRF) of Korea, grants from Ministry of Science and ICT through the National Research Foundation (NRF) of Korea, during the conduct of the study. The other authors have no conflicts of interest to declare.

Références

J Gastrointest Surg. 2015 Nov;19(11):2079-92
pubmed: 26063080
Clin Chim Acta. 2019 Jun;493:1-7
pubmed: 30796899
Ann Med Surg (Lond). 2018 Aug 23;34:4-10
pubmed: 30181871
J Surg Res. 2004 Jan;116(1):181-6
pubmed: 14732366
J Anim Physiol Anim Nutr (Berl). 2008 Jun;92(3):272-83
pubmed: 18477307
Anal Bioanal Chem. 2016 Jul;408(18):4975-85
pubmed: 27178550
Anal Chem. 2017 May 2;89(9):4969-4977
pubmed: 28399627
Scand J Clin Lab Invest. 1987 Oct;47(6):613-7
pubmed: 3672034
Proc Natl Acad Sci U S A. 1996 Nov 12;93(23):13280-5
pubmed: 8917582
World J Surg. 2007 Aug;31(8):1643-51
pubmed: 17551779
BMC Gastroenterol. 2017 Apr 20;17(1):57
pubmed: 28427335
Hepatology. 2008 Oct;48(4):1097-105
pubmed: 18697204
Biochem J. 1978 Jan 15;170(1):1-8
pubmed: 24443
J Lipid Res. 1970 Nov;11(6):536-43
pubmed: 5504519
Hepatology. 2004 Dec;40(6):1252-5
pubmed: 15558710
Biochim Biophys Acta. 2012 Sep;1822(9):1442-52
pubmed: 22627108
Hepatobiliary Pancreat Dis Int. 2014 Aug;13(4):361-70
pubmed: 25100120
Oxid Med Cell Longev. 2014;2014:906965
pubmed: 24799983
Nat Rev Drug Discov. 2005 Jul;4(7):594-610
pubmed: 16052242
Hepatology. 2019 Jan;69(1):329-342
pubmed: 30022502
Ann Surg. 2005 Dec;242(6):824-8, discussion 828-9
pubmed: 16327492
Ann Surg. 2016 Mar;263(3):546-56
pubmed: 25775061
Arch Surg. 2008 Mar;143(3):247-53; discussion 253
pubmed: 18347271
Int J Hepatol. 2012;2012:549241
pubmed: 22319652
Biochim Biophys Acta. 1962 Nov 19;65:128-35
pubmed: 13948499
PLoS One. 2017 Oct 18;12(10):e0185685
pubmed: 29045432
Sci Rep. 2020 Jun 19;10(1):9960
pubmed: 32561884
Scand J Gastroenterol. 2018 Oct - Nov;53(10-11):1335-1339
pubmed: 30345846
Hepatology. 1998 May;27(5):1354-61
pubmed: 9581691
J Hepatobiliary Pancreat Sci. 2017 Jul;24(7):E6-E7
pubmed: 28672427
J Korean Med Sci. 2014 Sep;29 Suppl 2:S155-63
pubmed: 25317020
Biochem J. 1991 Aug 1;277 ( Pt 3):723-8
pubmed: 1872808
J Mass Spectrom. 2012 Aug;47(8):1004-14
pubmed: 22899509
Biochem J. 1988 Aug 1;253(3):693-701
pubmed: 3178736
Surg Today. 1997;27(6):518-26
pubmed: 9306545
J Gastrointest Surg. 2016 Mar;20(3):587-94
pubmed: 26573852
Scand J Gastroenterol. 2010 Apr;45(4):468-76
pubmed: 20082593
J Surg Res. 2011 Oct;170(2):e233-42
pubmed: 21816413
Hepatobiliary Surg Nutr. 2014 Oct;3(5):238-46
pubmed: 25392835
Gastroenterology. 2003 Aug;125(2):437-43
pubmed: 12891546
J Hepatobiliary Pancreat Surg. 1999;6(3):275-80
pubmed: 10526063
Surgery. 2011 May;149(5):713-24
pubmed: 21236455

Auteurs

Hye-Sung Jo (HS)

Department of Surgery, Korea University College of Medicine, Seoul, Korea.

Hae A Kim (HA)

Department of Chemistry, Yonsei University, Seoul, Korea.

Jong Cheol Lee (JC)

Department of Chemistry, Yonsei University, Seoul, Korea.

Kyung Chul Yoon (KC)

Department of Surgery, Korea University College of Medicine, Seoul, Korea.

Young-In Yoon (YI)

Department of Surgery, University of Ulsan College of Medicine, Seoul, Korea.

Yoon Young Choi (YY)

Department of Biomedical Science, Korea University College of Medicine Graduate School, Seoul, Korea.

Jin-I Seok (JI)

Department of Biomedical Science, Korea University College of Medicine Graduate School, Seoul, Korea.

Myeong Hee Moon (MH)

Department of Chemistry, Yonsei University, Seoul, Korea.

Dong-Sik Kim (DS)

Department of Surgery, Korea University College of Medicine, Seoul, Korea.

Classifications MeSH