Genetic variation in PNPLA3 but not APOC3 influences liver fat in non-alcoholic fatty liver disease

Background and Aim:  A recent study in Indian subjects suggested common variants in apolipoprotein C3 (APOC3) (T‐455C at rs2854116 and C‐482T at rs2854117) to contribute to non‐alcoholic fatty liver disease (NAFLD), plasma apoC3 and triglyceride concentrations. Our aim was to determine the contribut...

Full description

Saved in:
Bibliographic Details
Published inJournal of gastroenterology and hepatology Vol. 27; no. 5; pp. 951 - 956
Main Authors Hyysalo, Jenni, Stojkovic, Ivana, Kotronen, Anna, Hakkarainen, Antti, Sevastianova, Ksenia, Makkonen, Janne, Lundbom, Nina, Rissanen, Aila, Krauss, Ronald M, Melander, Olle, Orho-Melander, Marju, Yki-Järvinen, Hannele
Format Journal Article
LanguageEnglish
Published Melbourne, Australia Blackwell Publishing Asia 01.05.2012
Subjects
Online AccessGet full text
ISSN0815-9319
1440-1746
1440-1746
DOI10.1111/j.1440-1746.2011.07045.x

Cover

Abstract Background and Aim:  A recent study in Indian subjects suggested common variants in apolipoprotein C3 (APOC3) (T‐455C at rs2854116 and C‐482T at rs2854117) to contribute to non‐alcoholic fatty liver disease (NAFLD), plasma apoC3 and triglyceride concentrations. Our aim was to determine the contribution of genetic variation in APOC3 on liver fat content and plasma triglyceride and apoC3 concentrations in a larger European cohort. Methods:  A total of 417 Finnish individuals were genotyped for rs2854116 and rs2854117 in APOC3 and the known rs738409 in patatin‐like phospholipase domain‐containing protein 3 (PNPLA3) influencing liver fat. Plasma apoC3 concentration was measured enzymatically, and liver fat by proton magnetic resonance spectroscopy. Results:  APOC3 wild‐type homozygotes and variant allele (T‐455C or C‐482T or both) carriers did not differ with regard to liver fat, apoC3 concentrations, triglyceride‐, high density lipoprotein‐, fasting plasma glucose, insulin‐, alanine aminotransferase‐ and aspartate aminotransferase‐concentrations, nor was there a difference in prevalence of NAFLD. In contrast, carriers of the PNPLA3 GG genotype at rs738409 had a 2.7‐fold (median 11.3%) higher liver fat than those with the CC (median 4.2%) genotype. The PNPLA3 rs738409 was also an independent predictor of liver fat, together with age, gender, and body mass index. Conclusion:  Genetic variants in PNPLA3 but not APOC3 contribute to the variance in liver fat content due to NAFLD.
AbstractList Background and Aim:  A recent study in Indian subjects suggested common variants in apolipoprotein C3 ( APOC3 ) (T‐455C at rs2854116 and C‐482T at rs2854117) to contribute to non‐alcoholic fatty liver disease (NAFLD), plasma apoC3 and triglyceride concentrations. Our aim was to determine the contribution of genetic variation in APOC3 on liver fat content and plasma triglyceride and apoC3 concentrations in a larger European cohort. Methods:  A total of 417 Finnish individuals were genotyped for rs2854116 and rs2854117 in APOC3 and the known rs738409 in patatin‐like phospholipase domain‐containing protein 3 ( PNPLA3 ) influencing liver fat. Plasma apoC3 concentration was measured enzymatically, and liver fat by proton magnetic resonance spectroscopy. Results:  APOC3 wild‐type homozygotes and variant allele (T‐455C or C‐482T or both) carriers did not differ with regard to liver fat, apoC3 concentrations, triglyceride‐, high density lipoprotein‐, fasting plasma glucose, insulin‐, alanine aminotransferase‐ and aspartate aminotransferase‐concentrations, nor was there a difference in prevalence of NAFLD. In contrast, carriers of the PNPLA3 GG genotype at rs738409 had a 2.7‐fold (median 11.3%) higher liver fat than those with the CC (median 4.2%) genotype. The PNPLA3 rs738409 was also an independent predictor of liver fat, together with age, gender, and body mass index. Conclusion:  Genetic variants in PNPLA3 but not APOC3 contribute to the variance in liver fat content due to NAFLD.
Background and Aim:  A recent study in Indian subjects suggested common variants in apolipoprotein C3 (APOC3) (T‐455C at rs2854116 and C‐482T at rs2854117) to contribute to non‐alcoholic fatty liver disease (NAFLD), plasma apoC3 and triglyceride concentrations. Our aim was to determine the contribution of genetic variation in APOC3 on liver fat content and plasma triglyceride and apoC3 concentrations in a larger European cohort. Methods:  A total of 417 Finnish individuals were genotyped for rs2854116 and rs2854117 in APOC3 and the known rs738409 in patatin‐like phospholipase domain‐containing protein 3 (PNPLA3) influencing liver fat. Plasma apoC3 concentration was measured enzymatically, and liver fat by proton magnetic resonance spectroscopy. Results:  APOC3 wild‐type homozygotes and variant allele (T‐455C or C‐482T or both) carriers did not differ with regard to liver fat, apoC3 concentrations, triglyceride‐, high density lipoprotein‐, fasting plasma glucose, insulin‐, alanine aminotransferase‐ and aspartate aminotransferase‐concentrations, nor was there a difference in prevalence of NAFLD. In contrast, carriers of the PNPLA3 GG genotype at rs738409 had a 2.7‐fold (median 11.3%) higher liver fat than those with the CC (median 4.2%) genotype. The PNPLA3 rs738409 was also an independent predictor of liver fat, together with age, gender, and body mass index. Conclusion:  Genetic variants in PNPLA3 but not APOC3 contribute to the variance in liver fat content due to NAFLD.
A recent study in Indian subjects suggested common variants in apolipoprotein C3 (APOC3) (T-455C at rs2854116 and C-482T at rs2854117) to contribute to non-alcoholic fatty liver disease (NAFLD), plasma apoC3 and triglyceride concentrations. Our aim was to determine the contribution of genetic variation in APOC3 on liver fat content and plasma triglyceride and apoC3 concentrations in a larger European cohort. A total of 417 Finnish individuals were genotyped for rs2854116 and rs2854117 in APOC3 and the known rs738409 in patatin-like phospholipase domain-containing protein 3 (PNPLA3) influencing liver fat. Plasma apoC3 concentration was measured enzymatically, and liver fat by proton magnetic resonance spectroscopy. APOC3 wild-type homozygotes and variant allele (T-455C or C-482T or both) carriers did not differ with regard to liver fat, apoC3 concentrations, triglyceride-, high density lipoprotein-, fasting plasma glucose, insulin-, alanine aminotransferase- and aspartate aminotransferase-concentrations, nor was there a difference in prevalence of NAFLD. In contrast, carriers of the PNPLA3 GG genotype at rs738409 had a 2.7-fold (median 11.3%) higher liver fat than those with the CC (median 4.2%) genotype. The PNPLA3 rs738409 was also an independent predictor of liver fat, together with age, gender, and body mass index. Genetic variants in PNPLA3 but not APOC3 contribute to the variance in liver fat content due to NAFLD.
A recent study in Indian subjects suggested common variants in apolipoprotein C3 (APOC3) (T-455C at rs2854116 and C-482T at rs2854117) to contribute to non-alcoholic fatty liver disease (NAFLD), plasma apoC3 and triglyceride concentrations. Our aim was to determine the contribution of genetic variation in APOC3 on liver fat content and plasma triglyceride and apoC3 concentrations in a larger European cohort.BACKGROUND AND AIMA recent study in Indian subjects suggested common variants in apolipoprotein C3 (APOC3) (T-455C at rs2854116 and C-482T at rs2854117) to contribute to non-alcoholic fatty liver disease (NAFLD), plasma apoC3 and triglyceride concentrations. Our aim was to determine the contribution of genetic variation in APOC3 on liver fat content and plasma triglyceride and apoC3 concentrations in a larger European cohort.A total of 417 Finnish individuals were genotyped for rs2854116 and rs2854117 in APOC3 and the known rs738409 in patatin-like phospholipase domain-containing protein 3 (PNPLA3) influencing liver fat. Plasma apoC3 concentration was measured enzymatically, and liver fat by proton magnetic resonance spectroscopy.METHODSA total of 417 Finnish individuals were genotyped for rs2854116 and rs2854117 in APOC3 and the known rs738409 in patatin-like phospholipase domain-containing protein 3 (PNPLA3) influencing liver fat. Plasma apoC3 concentration was measured enzymatically, and liver fat by proton magnetic resonance spectroscopy.APOC3 wild-type homozygotes and variant allele (T-455C or C-482T or both) carriers did not differ with regard to liver fat, apoC3 concentrations, triglyceride-, high density lipoprotein-, fasting plasma glucose, insulin-, alanine aminotransferase- and aspartate aminotransferase-concentrations, nor was there a difference in prevalence of NAFLD. In contrast, carriers of the PNPLA3 GG genotype at rs738409 had a 2.7-fold (median 11.3%) higher liver fat than those with the CC (median 4.2%) genotype. The PNPLA3 rs738409 was also an independent predictor of liver fat, together with age, gender, and body mass index.RESULTSAPOC3 wild-type homozygotes and variant allele (T-455C or C-482T or both) carriers did not differ with regard to liver fat, apoC3 concentrations, triglyceride-, high density lipoprotein-, fasting plasma glucose, insulin-, alanine aminotransferase- and aspartate aminotransferase-concentrations, nor was there a difference in prevalence of NAFLD. In contrast, carriers of the PNPLA3 GG genotype at rs738409 had a 2.7-fold (median 11.3%) higher liver fat than those with the CC (median 4.2%) genotype. The PNPLA3 rs738409 was also an independent predictor of liver fat, together with age, gender, and body mass index.Genetic variants in PNPLA3 but not APOC3 contribute to the variance in liver fat content due to NAFLD.CONCLUSIONGenetic variants in PNPLA3 but not APOC3 contribute to the variance in liver fat content due to NAFLD.
Background and Aim: A recent study in Indian subjects suggested common variants in apolipoprotein C3 (APOC3) (T-455C at rs2854116 and C-482T at rs2854117) to contribute to non-alcoholic fatty liver disease (NAFLD), plasma apoC3 and triglyceride concentrations. Our aim was to determine the contribution of genetic variation in APOC3 on liver fat content and plasma triglyceride and apoC3 concentrations in a larger European cohort. Methods: Atotal of 417 Finnish individuals were genotyped for rs2854116 and rs2854117 in APOC3 and the known rs738409 in patatin-like phospholipase domain-containing protein 3 (PNPLA3) influencing liver fat. Plasma apoC3 concentration was measured enzymatically, and liver fat by proton magnetic resonance spectroscopy. Results: APOC3 wild-type homozygotes and variant allele (T-455C or C-482T or both) carriers did not differ with regard to liver fat, apoC3 concentrations, triglyceride-, high density lipoprotein-, fasting plasma glucose, insulin-, alanine aminotransferase-and aspartate aminotransferase-concentrations, nor was there a difference in prevalence of NAFLD. In contrast, carriers of the PNPLA3 GG genotype at rs738409 had a 2.7-fold (median 11.3%) higher liver fat than those with the CC (median 4.2%) genotype. The PNPLA3 rs738409 was also an independent predictor of liver fat, together with age, gender, and body mass index. Conclusion: Genetic variants in PNPLA3 but not APOC3 contribute to the variance in liver fat content due to NAFLD.
Author Sevastianova, Ksenia
Krauss, Ronald M
Kotronen, Anna
Hyysalo, Jenni
Hakkarainen, Antti
Rissanen, Aila
Yki-Järvinen, Hannele
Stojkovic, Ivana
Lundbom, Nina
Orho-Melander, Marju
Makkonen, Janne
Melander, Olle
Author_xml – sequence: 1
  givenname: Jenni
  surname: Hyysalo
  fullname: Hyysalo, Jenni
  organization: Department of Medicine, Division of Diabetes, Helsinki University Central Hospital, Finland
– sequence: 2
  givenname: Ivana
  surname: Stojkovic
  fullname: Stojkovic, Ivana
  organization: Department of Clinical Sciences, Diabetes and Endocrinology, University Hospital Malmö, Lund University, Malmö, Sweden
– sequence: 3
  givenname: Anna
  surname: Kotronen
  fullname: Kotronen, Anna
  organization: Department of Medicine, Division of Diabetes, Helsinki University Central Hospital, Finland
– sequence: 4
  givenname: Antti
  surname: Hakkarainen
  fullname: Hakkarainen, Antti
  organization: Department of Medicine, Division of Diabetes, Helsinki University Central Hospital, Finland
– sequence: 5
  givenname: Ksenia
  surname: Sevastianova
  fullname: Sevastianova, Ksenia
  organization: Department of Medicine, Division of Diabetes, Helsinki University Central Hospital, Finland
– sequence: 6
  givenname: Janne
  surname: Makkonen
  fullname: Makkonen, Janne
  organization: Department of Medicine, Division of Diabetes, Helsinki University Central Hospital, Finland
– sequence: 7
  givenname: Nina
  surname: Lundbom
  fullname: Lundbom, Nina
  organization: Department of Radiology, Helsinki University Central Hospital, Finland
– sequence: 8
  givenname: Aila
  surname: Rissanen
  fullname: Rissanen, Aila
  organization: Obesity Research Unit, Department of Psychiatry, Helsinki University Central Hospital, Finland
– sequence: 9
  givenname: Ronald M
  surname: Krauss
  fullname: Krauss, Ronald M
  organization: Department of Clinical Sciences, Diabetes and Endocrinology, University Hospital Malmö, Lund University, Malmö, Sweden
– sequence: 10
  givenname: Olle
  surname: Melander
  fullname: Melander, Olle
  organization: Department of Clinical Sciences, Diabetes and Endocrinology, University Hospital Malmö, Lund University, Malmö, Sweden
– sequence: 11
  givenname: Marju
  surname: Orho-Melander
  fullname: Orho-Melander, Marju
  organization: Department of Clinical Sciences, Diabetes and Endocrinology, University Hospital Malmö, Lund University, Malmö, Sweden
– sequence: 12
  givenname: Hannele
  surname: Yki-Järvinen
  fullname: Yki-Järvinen, Hannele
  email: ykijarvi@cc.helsinki.fi
  organization: Department of Medicine, Division of Diabetes, Helsinki University Central Hospital, Finland
BackLink https://www.ncbi.nlm.nih.gov/pubmed/22141340$$D View this record in MEDLINE/PubMed
BookMark eNqNUU1v0zAYjtAQ6wZ_AeXIJcGOv5IDSFWBjql0FQLt-Mpx3mguaVLsZGv_PU7b9cBpvth6_XzZz1V00XYtRlFMSUrD-rhOKeckoYrLNCOUpkQRLtLdq2hyvriIJiSnIikYLS6jK-_XhBBOlHgTXWYZ5ZRxMonMHFvsrYkftbO6t10b2zZeLVeLKYvLoY_bro-nq7sZC_O6GbA16OPGPqKLa92P4JAt0Y3pHrom6IRhvz8BKutRe3wbva514_Hdab-Ofn_7-mt2kyzu5t9n00ViBFcikVnFqTDSZEygISViZhRTeV1WGlFWNSuI1EphUSDPSyIoEXmVGWYk8oxqdh3po65_wu1QwtbZjXZ76LSFbed63YDDkMiZB2gG8AgBFTIfnu2B1EYWFaNgJOfAuWKgWZ5BZTSTtWJZbkTw-HD02Lru74C-h431BptGt9gNHiihUiqhchag70_QodxgdY7z_PkB8PkIMK7z3mENxvaHML3TtglaMLYNaxhLhbFUGNuGQ9uwCwL5fwLPHi-gfjpSn2yD-xfz4HZ-M54CPznyre9xd-Zr9wdkKE3A_XIOtz_Jj_vZlyUw9g_3eNBW
CitedBy_id crossref_primary_10_1016_j_atherosclerosis_2016_12_018
crossref_primary_10_1097_JCMA_0000000000000564
crossref_primary_10_1007_s12328_017_0732_5
crossref_primary_10_1080_17474124_2020_1780915
crossref_primary_10_3390_antiox10020270
crossref_primary_10_3748_wjg_v21_i39_11088
crossref_primary_10_3923_ajbmb_2018_16_22
crossref_primary_10_1016_j_molmet_2021_101238
crossref_primary_10_3389_fgene_2022_971484
crossref_primary_10_1016_j_molmet_2020_101092
crossref_primary_10_3390_biomedicines11010106
crossref_primary_10_1016_j_clnu_2024_10_007
crossref_primary_10_3390_children4060049
crossref_primary_10_1016_j_tem_2014_08_001
crossref_primary_10_1155_2020_8869674
crossref_primary_10_1371_journal_pone_0108381
crossref_primary_10_1007_s12263_014_0388_4
crossref_primary_10_1111_ijpo_12852
crossref_primary_10_1111_jgh_16521
crossref_primary_10_15406_bbij_2018_07_00227
crossref_primary_10_1002_iub_2302
crossref_primary_10_3390_v15081724
crossref_primary_10_1016_j_flm_2017_10_002
crossref_primary_10_1111_apt_12609
crossref_primary_10_5812_hepatmon_23100
crossref_primary_10_1002_hep_26672
crossref_primary_10_1097_MPG_0000000000001979
crossref_primary_10_3390_ijms19030911
crossref_primary_10_1016_j_ygeno_2013_03_007
crossref_primary_10_1111_jgh_12656
crossref_primary_10_5223_pghn_2021_24_5_455
crossref_primary_10_3748_wjg_v20_i38_14010
crossref_primary_10_1007_s12664_014_0504_9
crossref_primary_10_1007_s10620_016_4120_7
crossref_primary_10_1002_oby_20366
crossref_primary_10_1111_obr_12820
crossref_primary_10_1002_oby_20523
crossref_primary_10_1016_j_tips_2015_07_001
crossref_primary_10_3748_wjg_v20_i36_12956
crossref_primary_10_1586_1744666X_2013_816484
crossref_primary_10_1111_j_1440_1746_2012_07103_x
Cites_doi 10.1152/ajpendo.00381.2004
10.1152/ajpendo.00444.2007
10.1097/00004424-199304000-00006
10.1152/ajpendo.00064.2004
10.1002/hep.24567
10.1093/qjmed/hcl027
10.1210/jc.2007-0482
10.1002/hep.24659
10.1210/jc.2003-032056
10.1016/S0140-6736(05)67402-8
10.1038/oby.2009.326
10.1016/j.atherosclerosis.2010.02.025
10.1056/NEJMoa0907295
10.1007/s00125-009-1285-z
10.1194/jlr.M500455-JLR200
10.1161/CIRCULATIONAHA.109.875807
10.1042/CS20070308
10.1016/j.arcmed.2006.10.013
10.1002/hep.24283
10.1161/01.ATV.0000064383.88696.24
ContentType Journal Article
Copyright 2011 Journal of Gastroenterology and Hepatology Foundation and Blackwell Publishing Asia Pty Ltd
2011 Journal of Gastroenterology and Hepatology Foundation and Blackwell Publishing Asia Pty Ltd.
Copyright_xml – notice: 2011 Journal of Gastroenterology and Hepatology Foundation and Blackwell Publishing Asia Pty Ltd
– notice: 2011 Journal of Gastroenterology and Hepatology Foundation and Blackwell Publishing Asia Pty Ltd.
CorporateAuthor Lunds universitet
Profile areas and other strong research environments
Department of Clinical Sciences, Malmö
Lund University
Kardiovaskulär forskning - hypertoni
Diabetes - Cardiovascular Disease
Strategiska forskningsområden (SFO)
EpiHealth: Epidemiology for Health
EXODIAB: Excellence of Diabetes Research in Sweden
Faculty of Medicine
Strategic research areas (SRA)
Diabetes - kardiovaskulär sjukdom
Medicinska fakulteten
Profilområden och andra starka forskningsmiljöer
Institutionen för kliniska vetenskaper, Malmö
Cardiovascular Research - Hypertension
CorporateAuthor_xml – name: Faculty of Medicine
– name: Medicinska fakulteten
– name: Diabetes - kardiovaskulär sjukdom
– name: Strategiska forskningsområden (SFO)
– name: Cardiovascular Research - Hypertension
– name: Kardiovaskulär forskning - hypertoni
– name: EpiHealth: Epidemiology for Health
– name: Institutionen för kliniska vetenskaper, Malmö
– name: Strategic research areas (SRA)
– name: Lunds universitet
– name: Diabetes - Cardiovascular Disease
– name: Profilområden och andra starka forskningsmiljöer
– name: Lund University
– name: EXODIAB: Excellence of Diabetes Research in Sweden
– name: Profile areas and other strong research environments
– name: Department of Clinical Sciences, Malmö
DBID BSCLL
AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
7X8
ADTPV
AOWAS
D95
DOI 10.1111/j.1440-1746.2011.07045.x
DatabaseName Istex
CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
MEDLINE - Academic
SwePub
SwePub Articles
SWEPUB Lunds universitet
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
MEDLINE - Academic
DatabaseTitleList CrossRef

MEDLINE
MEDLINE - Academic

Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 1440-1746
EndPage 956
ExternalDocumentID oai_portal_research_lu_se_publications_0fc69d31_c644_4473_a382_dca36f7328c5
22141340
10_1111_j_1440_1746_2011_07045_x
JGH7045
ark_67375_WNG_JR0MWCDN_3
Genre article
Research Support, Non-U.S. Gov't
Journal Article
GeographicLocations Finland
GeographicLocations_xml – name: Finland
GroupedDBID ---
.3N
.GA
.Y3
05W
0R~
10A
1OB
1OC
29K
31~
33P
36B
3SF
4.4
50Y
50Z
51W
51X
52M
52N
52O
52P
52R
52S
52T
52U
52V
52W
52X
53G
5GY
5HH
5LA
5VS
66C
702
7PT
8-0
8-1
8-3
8-4
8-5
8UM
930
A01
A03
AAESR
AAEVG
AAHQN
AAIPD
AAMMB
AAMNL
AANHP
AANLZ
AAONW
AASGY
AAXRX
AAYCA
AAZKR
ABCQN
ABCUV
ABEML
ABJNI
ABPVW
ABQWH
ABXGK
ACAHQ
ACBWZ
ACCZN
ACGFS
ACGOF
ACMXC
ACPOU
ACPRK
ACRPL
ACSCC
ACXBN
ACXQS
ACYXJ
ADBBV
ADBTR
ADEOM
ADIZJ
ADKYN
ADMGS
ADNMO
ADOZA
ADXAS
ADZMN
AEFGJ
AEGXH
AEIGN
AEIMD
AENEX
AEUYR
AEYWJ
AFBPY
AFEBI
AFFPM
AFGKR
AFWVQ
AFZJQ
AGHNM
AGQPQ
AGXDD
AGYGG
AHBTC
AHEFC
AIACR
AIDQK
AIDYY
AIQQE
AITYG
AIURR
ALAGY
ALMA_UNASSIGNED_HOLDINGS
ALUQN
ALVPJ
AMBMR
AMYDB
ASPBG
ATUGU
AVWKF
AZBYB
AZFZN
AZVAB
BAFTC
BDRZF
BFHJK
BHBCM
BMXJE
BROTX
BRXPI
BSCLL
BY8
C45
CAG
COF
CS3
D-6
D-7
D-E
D-F
D-I
DCZOG
DPXWK
DR2
DRFUL
DRMAN
DRSTM
DTERQ
DU5
EBS
EJD
EMOBN
EX3
F00
F01
F04
F5P
FEDTE
FUBAC
FZ0
G-S
G.N
GODZA
H.X
HF~
HGLYW
HVGLF
HZI
HZ~
IHE
IX1
J0M
K48
KBYEO
KMS
LATKE
LC2
LC3
LEEKS
LH4
LITHE
LOXES
LP6
LP7
LUTES
LW6
LYRES
MEWTI
MK4
MRFUL
MRMAN
MRSTM
MSFUL
MSMAN
MSSTM
MXFUL
MXMAN
MXSTM
N04
N05
N9A
NF~
O66
O9-
OIG
OVD
P2P
P2W
P2X
P2Z
P4B
P4D
PALCI
Q.N
Q11
QB0
R.K
RIWAO
RJQFR
ROL
RX1
SAMSI
SUPJJ
TEORI
UB1
W8V
W99
WBKPD
WH7
WHWMO
WIH
WIJ
WIK
WOHZO
WOQ
WOW
WQJ
WVDHM
WXI
WXSBR
XG1
YFH
ZZTAW
~IA
~WT
AAHHS
AAYXX
ACCFJ
AEEZP
AEQDE
AIWBW
AJBDE
CITATION
AEUQT
AFPWT
CGR
CUY
CVF
ECM
EIF
ESX
NPM
WRC
WUP
7X8
ADTPV
AOWAS
D95
ID FETCH-LOGICAL-c5475-62d415c6c235ec0bee2c7378fbdaee6df3906a77e99e48b051058d2c3c6e421a3
IEDL.DBID DR2
ISSN 0815-9319
1440-1746
IngestDate Tue Sep 09 23:29:11 EDT 2025
Fri Sep 05 13:17:43 EDT 2025
Wed Feb 19 01:49:12 EST 2025
Thu Apr 24 22:59:42 EDT 2025
Tue Jul 01 01:44:59 EDT 2025
Sun Sep 21 06:23:30 EDT 2025
Sun Sep 21 06:29:20 EDT 2025
IsDoiOpenAccess false
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 5
Language English
License 2011 Journal of Gastroenterology and Hepatology Foundation and Blackwell Publishing Asia Pty Ltd.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c5475-62d415c6c235ec0bee2c7378fbdaee6df3906a77e99e48b051058d2c3c6e421a3
Notes istex:49F5B67F899B176C6871EE25B0C08BCC1A39975E
ArticleID:JGH7045
ark:/67375/WNG-JR0MWCDN-3
These authors contributed equally to this work.
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
OpenAccessLink https://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/j.1440-1746.2011.07045.x
PMID 22141340
PQID 1016675783
PQPubID 23479
PageCount 6
ParticipantIDs swepub_primary_oai_portal_research_lu_se_publications_0fc69d31_c644_4473_a382_dca36f7328c5
proquest_miscellaneous_1016675783
pubmed_primary_22141340
crossref_citationtrail_10_1111_j_1440_1746_2011_07045_x
crossref_primary_10_1111_j_1440_1746_2011_07045_x
wiley_primary_10_1111_j_1440_1746_2011_07045_x_JGH7045
istex_primary_ark_67375_WNG_JR0MWCDN_3
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate May 2012
PublicationDateYYYYMMDD 2012-05-01
PublicationDate_xml – month: 05
  year: 2012
  text: May 2012
PublicationDecade 2010
PublicationPlace Melbourne, Australia
PublicationPlace_xml – name: Melbourne, Australia
– name: Australia
PublicationTitle Journal of gastroenterology and hepatology
PublicationTitleAlternate J Gastroenterol Hepatol
PublicationYear 2012
Publisher Blackwell Publishing Asia
Publisher_xml – name: Blackwell Publishing Asia
References Kotronen A, Yki-Jarvinen H, Sevastianova K et al. Comparison of the relative contributions of intra-abdominal and liver fat to components of the metabolic syndrome. Obesity (Silver Spring) 2010; 18: 937-44.
Alberti KG, Zimmet P, Shaw J. The metabolic syndrome-a new worldwide definition. Lancet 2005; 366: 1059-62.
Sookoian S, Pirola CJ. Meta-analysis of the influence of I148M variant of patatin-like phospholipase domain containing 3 gene (PNPLA3) on the susceptibility and histological severity of nonalcoholic fatty liver disease. Hepatology 2011; 53: 1883-94.
Miller M, Rhyne J, Chen H et al. APOC3 promoter polymorphisms C-482T and T-455C are associated with the metabolic syndrome. Arch. Med. Res. 2007; 38: 444-57.
Li X, Zhao Q, Wu K, Fan D. I148M variant of PNPLA3 confer increased risk for nonalcoholic fatty liver disease not only in European population, but also in Chinese population. Hepatology 2011; 54: 2276.
Li Y, Xing C, Cohen JC, Hobbs HH. Genetic variant in PNPLA3 associated with nonalcoholic fatty liver disease in China. Hepatology 2012; 55: 327-8.
Longo R, Ricci C, Masutti F et al. Fatty infiltration of the liver. Quantification by 1H localized magnetic resonance spectroscopy and comparison with computed tomography. Invest. Radiol. 1993; 28: 297-302.
Cohn JS, Patterson BW, Uffelman KD, Davignon J, Steiner G. Rate of production of plasma and very-low-density lipoprotein (VLDL) apolipoprotein C-III is strongly related to the concentration and level of production of VLDL triglyceride in male subjects with different body weights and levels of insulin sensitivity. J. Clin. Endocrinol. Metab. 2004; 89: 3949-55.
Szczepaniak LS, Nurenberg P, Leonard D et al. Magnetic resonance spectroscopy to measure hepatic triglyceride content: prevalence of hepatic steatosis in the general population. Am. J. Physiol. Endocrinol. Metab. 2005; 288: E462-8.
Ooi EM, Barrett PH, Chan DC, Watts GF. Apolipoprotein C-III: understanding an emerging cardiovascular risk factor. Clin. Sci. 2008; 114: 611-24.
Pietilainen KH, Rissanen A, Kaprio J et al. Acquired obesity is associated with increased liver fat, intra-abdominal fat, and insulin resistance in young adult monozygotic twins. Am. J. Physiol. Endocrinol. Metab. 2005; 288: E768-74.
Skogsberg J, Kannisto K, Cassel TN, Hamsten A, Eriksson P, Ehrenborg E. Evidence that peroxisome proliferator-activated receptor delta influences cholesterol metabolism in men. Arterioscler. Thromb. Vasc. Biol. 2003; 23: 637-43.
Kotronen A, Johansson LE, Johansson LM et al. A common variant in PNPLA3, which encodes adiponutrin, is associated with liver fat content in humans. Diabetologia 2009; 52: 1056-60.
Mauger JF, Couture P, Bergeron N, Lamarche B. Apolipoprotein C-III isoforms: kinetics and relative implication in lipid metabolism. J. Lipid Res. 2006; 47: 1212-18.
Kotronen A, Westerbacka J, Bergholm R, Pietilainen KH, Yki-Jarvinen H. Liver fat in the metabolic syndrome. J. Clin. Endocrinol. Metab. 2007; 92: 3490-7.
Petersen KF, Dufour S, Hariri A et al. Apolipoprotein C3 gene variants in nonalcoholic fatty liver disease. N. Engl. J. Med. 2010; 362: 1082-9.
Chan DC, Watts GF. Apolipoproteins as markers and managers of coronary risk. QJM 2006; 99: 277-87.
Zheng C, Khoo C, Furtado J, Sacks FM. Apolipoprotein C-III and the metabolic basis for hypertriglyceridemia and the dense low-density lipoprotein phenotype. Circulation 2010; 121: 1722-34.
Kotronen A, Vehkavaara S, Seppala-Lindroos A, Bergholm R, Yki-Jarvinen H. Effect of liver fat on insulin clearance. Am. J. Physiol. Endocrinol. Metab. 2007; 293: E1709-15.
Shin MJ, Krauss RM. Apolipoprotein CIII bound to apoB-containing lipoproteins is associated with small, dense LDL independent of plasma triglyceride levels in healthy men. Atherosclerosis 2010; 211: 337-41.
2009; 52
1993; 28
2007; 293
2005; 288
2010; 18
2006; 99
2005; 366
2006; 47
2004; 89
2010; 211
2011; 53
2010; 121
2007; 92
2011; 54
2010; 362
2008; 114
2012; 55
2003; 23
2007; 38
e_1_2_7_5_2
e_1_2_7_4_2
e_1_2_7_3_2
e_1_2_7_2_2
e_1_2_7_9_2
e_1_2_7_8_2
e_1_2_7_7_2
e_1_2_7_6_2
e_1_2_7_19_2
e_1_2_7_18_2
e_1_2_7_17_2
e_1_2_7_16_2
e_1_2_7_15_2
e_1_2_7_14_2
e_1_2_7_13_2
e_1_2_7_12_2
e_1_2_7_11_2
e_1_2_7_10_2
e_1_2_7_21_2
e_1_2_7_20_2
22369128 - J Gastroenterol Hepatol. 2012 May;27(5):848-51
References_xml – reference: Pietilainen KH, Rissanen A, Kaprio J et al. Acquired obesity is associated with increased liver fat, intra-abdominal fat, and insulin resistance in young adult monozygotic twins. Am. J. Physiol. Endocrinol. Metab. 2005; 288: E768-74.
– reference: Sookoian S, Pirola CJ. Meta-analysis of the influence of I148M variant of patatin-like phospholipase domain containing 3 gene (PNPLA3) on the susceptibility and histological severity of nonalcoholic fatty liver disease. Hepatology 2011; 53: 1883-94.
– reference: Li X, Zhao Q, Wu K, Fan D. I148M variant of PNPLA3 confer increased risk for nonalcoholic fatty liver disease not only in European population, but also in Chinese population. Hepatology 2011; 54: 2276.
– reference: Kotronen A, Vehkavaara S, Seppala-Lindroos A, Bergholm R, Yki-Jarvinen H. Effect of liver fat on insulin clearance. Am. J. Physiol. Endocrinol. Metab. 2007; 293: E1709-15.
– reference: Zheng C, Khoo C, Furtado J, Sacks FM. Apolipoprotein C-III and the metabolic basis for hypertriglyceridemia and the dense low-density lipoprotein phenotype. Circulation 2010; 121: 1722-34.
– reference: Kotronen A, Johansson LE, Johansson LM et al. A common variant in PNPLA3, which encodes adiponutrin, is associated with liver fat content in humans. Diabetologia 2009; 52: 1056-60.
– reference: Alberti KG, Zimmet P, Shaw J. The metabolic syndrome-a new worldwide definition. Lancet 2005; 366: 1059-62.
– reference: Mauger JF, Couture P, Bergeron N, Lamarche B. Apolipoprotein C-III isoforms: kinetics and relative implication in lipid metabolism. J. Lipid Res. 2006; 47: 1212-18.
– reference: Kotronen A, Yki-Jarvinen H, Sevastianova K et al. Comparison of the relative contributions of intra-abdominal and liver fat to components of the metabolic syndrome. Obesity (Silver Spring) 2010; 18: 937-44.
– reference: Li Y, Xing C, Cohen JC, Hobbs HH. Genetic variant in PNPLA3 associated with nonalcoholic fatty liver disease in China. Hepatology 2012; 55: 327-8.
– reference: Petersen KF, Dufour S, Hariri A et al. Apolipoprotein C3 gene variants in nonalcoholic fatty liver disease. N. Engl. J. Med. 2010; 362: 1082-9.
– reference: Longo R, Ricci C, Masutti F et al. Fatty infiltration of the liver. Quantification by 1H localized magnetic resonance spectroscopy and comparison with computed tomography. Invest. Radiol. 1993; 28: 297-302.
– reference: Skogsberg J, Kannisto K, Cassel TN, Hamsten A, Eriksson P, Ehrenborg E. Evidence that peroxisome proliferator-activated receptor delta influences cholesterol metabolism in men. Arterioscler. Thromb. Vasc. Biol. 2003; 23: 637-43.
– reference: Chan DC, Watts GF. Apolipoproteins as markers and managers of coronary risk. QJM 2006; 99: 277-87.
– reference: Cohn JS, Patterson BW, Uffelman KD, Davignon J, Steiner G. Rate of production of plasma and very-low-density lipoprotein (VLDL) apolipoprotein C-III is strongly related to the concentration and level of production of VLDL triglyceride in male subjects with different body weights and levels of insulin sensitivity. J. Clin. Endocrinol. Metab. 2004; 89: 3949-55.
– reference: Szczepaniak LS, Nurenberg P, Leonard D et al. Magnetic resonance spectroscopy to measure hepatic triglyceride content: prevalence of hepatic steatosis in the general population. Am. J. Physiol. Endocrinol. Metab. 2005; 288: E462-8.
– reference: Kotronen A, Westerbacka J, Bergholm R, Pietilainen KH, Yki-Jarvinen H. Liver fat in the metabolic syndrome. J. Clin. Endocrinol. Metab. 2007; 92: 3490-7.
– reference: Miller M, Rhyne J, Chen H et al. APOC3 promoter polymorphisms C-482T and T-455C are associated with the metabolic syndrome. Arch. Med. Res. 2007; 38: 444-57.
– reference: Shin MJ, Krauss RM. Apolipoprotein CIII bound to apoB-containing lipoproteins is associated with small, dense LDL independent of plasma triglyceride levels in healthy men. Atherosclerosis 2010; 211: 337-41.
– reference: Ooi EM, Barrett PH, Chan DC, Watts GF. Apolipoprotein C-III: understanding an emerging cardiovascular risk factor. Clin. Sci. 2008; 114: 611-24.
– volume: 52
  start-page: 1056
  year: 2009
  end-page: 60
  article-title: A common variant in PNPLA3, which encodes adiponutrin, is associated with liver fat content in humans
  publication-title: Diabetologia
– volume: 55
  start-page: 327
  year: 2012
  end-page: 8
  article-title: Genetic variant in PNPLA3 associated with nonalcoholic fatty liver disease in China
  publication-title: Hepatology
– volume: 89
  start-page: 3949
  year: 2004
  end-page: 55
  article-title: Rate of production of plasma and very‐low‐density lipoprotein (VLDL) apolipoprotein C‐III is strongly related to the concentration and level of production of VLDL triglyceride in male subjects with different body weights and levels of insulin sensitivity
  publication-title: J. Clin. Endocrinol. Metab.
– volume: 114
  start-page: 611
  year: 2008
  end-page: 24
  article-title: Apolipoprotein C‐III: understanding an emerging cardiovascular risk factor
  publication-title: Clin. Sci.
– volume: 293
  start-page: E1709
  year: 2007
  end-page: 15
  article-title: Effect of liver fat on insulin clearance
  publication-title: Am. J. Physiol. Endocrinol. Metab.
– volume: 288
  start-page: E768
  year: 2005
  end-page: 74
  article-title: Acquired obesity is associated with increased liver fat, intra‐abdominal fat, and insulin resistance in young adult monozygotic twins
  publication-title: Am. J. Physiol. Endocrinol. Metab.
– volume: 362
  start-page: 1082
  year: 2010
  end-page: 9
  article-title: Apolipoprotein C3 gene variants in nonalcoholic fatty liver disease
  publication-title: N. Engl. J. Med.
– volume: 366
  start-page: 1059
  year: 2005
  end-page: 62
  article-title: The metabolic syndrome—a new worldwide definition
  publication-title: Lancet
– volume: 121
  start-page: 1722
  year: 2010
  end-page: 34
  article-title: Apolipoprotein C‐III and the metabolic basis for hypertriglyceridemia and the dense low‐density lipoprotein phenotype
  publication-title: Circulation
– volume: 38
  start-page: 444
  year: 2007
  end-page: 57
  article-title: APOC3 promoter polymorphisms C‐482T and T‐455C are associated with the metabolic syndrome
  publication-title: Arch. Med. Res.
– volume: 23
  start-page: 637
  year: 2003
  end-page: 43
  article-title: Evidence that peroxisome proliferator‐activated receptor delta influences cholesterol metabolism in men
  publication-title: Arterioscler. Thromb. Vasc. Biol.
– volume: 28
  start-page: 297
  year: 1993
  end-page: 302
  article-title: Fatty infiltration of the liver. Quantification by 1H localized magnetic resonance spectroscopy and comparison with computed tomography
  publication-title: Invest. Radiol.
– volume: 54
  start-page: 2276
  year: 2011
  article-title: I148M variant of PNPLA3 confer increased risk for nonalcoholic fatty liver disease not only in European population, but also in Chinese population
  publication-title: Hepatology
– volume: 18
  start-page: 937
  year: 2010
  end-page: 44
  article-title: Comparison of the relative contributions of intra‐abdominal and liver fat to components of the metabolic syndrome
  publication-title: Obesity (Silver Spring)
– volume: 92
  start-page: 3490
  year: 2007
  end-page: 7
  article-title: Liver fat in the metabolic syndrome
  publication-title: J. Clin. Endocrinol. Metab.
– volume: 53
  start-page: 1883
  year: 2011
  end-page: 94
  article-title: Meta‐analysis of the influence of I148M variant of patatin‐like phospholipase domain containing 3 gene (PNPLA3) on the susceptibility and histological severity of nonalcoholic fatty liver disease
  publication-title: Hepatology
– volume: 288
  start-page: E462
  year: 2005
  end-page: 8
  article-title: Magnetic resonance spectroscopy to measure hepatic triglyceride content: prevalence of hepatic steatosis in the general population
  publication-title: Am. J. Physiol. Endocrinol. Metab.
– volume: 47
  start-page: 1212
  year: 2006
  end-page: 18
  article-title: Apolipoprotein C‐III isoforms: kinetics and relative implication in lipid metabolism
  publication-title: J. Lipid Res.
– volume: 211
  start-page: 337
  year: 2010
  end-page: 41
  article-title: Apolipoprotein CIII bound to apoB‐containing lipoproteins is associated with small, dense LDL independent of plasma triglyceride levels in healthy men
  publication-title: Atherosclerosis
– volume: 99
  start-page: 277
  year: 2006
  end-page: 87
  article-title: Apolipoproteins as markers and managers of coronary risk
  publication-title: QJM
– ident: e_1_2_7_2_2
  doi: 10.1152/ajpendo.00381.2004
– ident: e_1_2_7_13_2
  doi: 10.1152/ajpendo.00444.2007
– ident: e_1_2_7_11_2
  doi: 10.1097/00004424-199304000-00006
– ident: e_1_2_7_12_2
  doi: 10.1152/ajpendo.00064.2004
– ident: e_1_2_7_6_2
  doi: 10.1002/hep.24567
– ident: e_1_2_7_9_2
  doi: 10.1093/qjmed/hcl027
– ident: e_1_2_7_3_2
  doi: 10.1210/jc.2007-0482
– ident: e_1_2_7_7_2
  doi: 10.1002/hep.24659
– ident: e_1_2_7_18_2
  doi: 10.1210/jc.2003-032056
– ident: e_1_2_7_15_2
  doi: 10.1016/S0140-6736(05)67402-8
– ident: e_1_2_7_4_2
  doi: 10.1038/oby.2009.326
– ident: e_1_2_7_19_2
  doi: 10.1016/j.atherosclerosis.2010.02.025
– ident: e_1_2_7_8_2
  doi: 10.1056/NEJMoa0907295
– ident: e_1_2_7_10_2
  doi: 10.1007/s00125-009-1285-z
– ident: e_1_2_7_16_2
  doi: 10.1194/jlr.M500455-JLR200
– ident: e_1_2_7_17_2
  doi: 10.1161/CIRCULATIONAHA.109.875807
– ident: e_1_2_7_20_2
  doi: 10.1042/CS20070308
– ident: e_1_2_7_21_2
  doi: 10.1016/j.arcmed.2006.10.013
– ident: e_1_2_7_5_2
  doi: 10.1002/hep.24283
– ident: e_1_2_7_14_2
  doi: 10.1161/01.ATV.0000064383.88696.24
– reference: 22369128 - J Gastroenterol Hepatol. 2012 May;27(5):848-51
SSID ssj0004075
Score 2.2381392
Snippet Background and Aim:  A recent study in Indian subjects suggested common variants in apolipoprotein C3 (APOC3) (T‐455C at rs2854116 and C‐482T at rs2854117) to...
Background and Aim:  A recent study in Indian subjects suggested common variants in apolipoprotein C3 ( APOC3 ) (T‐455C at rs2854116 and C‐482T at rs2854117)...
A recent study in Indian subjects suggested common variants in apolipoprotein C3 (APOC3) (T-455C at rs2854116 and C-482T at rs2854117) to contribute to...
Background and Aim: A recent study in Indian subjects suggested common variants in apolipoprotein C3 (APOC3) (T-455C at rs2854116 and C-482T at rs2854117) to...
SourceID swepub
proquest
pubmed
crossref
wiley
istex
SourceType Open Access Repository
Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 951
SubjectTerms Adult
Age Factors
Alanine Transaminase - blood
Alleles
Analysis of Variance
Apolipoprotein C-III - blood
Apolipoprotein C-III - genetics
Aspartate Aminotransferases - blood
Blood Glucose - metabolism
Body Mass Index
Clinical Medicine
diabetes mellitus type 2
Fatty Liver - genetics
Fatty Liver - pathology
Female
Finland
Gastroenterologi och hepatologi
Gastroenterology and Hepatology
Homozygote
Humans
Insulin - blood
insulin resistance
Intra-Abdominal Fat
Klinisk medicin
Lipase - genetics
Lipoproteins, HDL - blood
Liver - pathology
Male
Medical and Health Sciences
Medicin och hälsovetenskap
Membrane Proteins - genetics
metabolic syndrome
Middle Aged
Non-alcoholic Fatty Liver Disease
Polymorphism, Single Nucleotide
proton magnetic resonance spectroscopy
Sex Factors
Statistics, Nonparametric
Triglycerides - blood
Title Genetic variation in PNPLA3 but not APOC3 influences liver fat in non-alcoholic fatty liver disease
URI https://api.istex.fr/ark:/67375/WNG-JR0MWCDN-3/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fj.1440-1746.2011.07045.x
https://www.ncbi.nlm.nih.gov/pubmed/22141340
https://www.proquest.com/docview/1016675783
Volume 27
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1ba9swFBajg7GX3S_eDQ3G3hxsSZbsx5CuDWHJQllp2YuQZJmOBKc0dmn3tJ-w37hfsnNsx2tKH8rYm9DNSP6O9Mk6_g4hHyIvjFQ2C41J4YAiUx5mNkHVfcmBLcMK2AjPT2dyfCgmx8lx5_-E_8K0-hD9Bze0jGa9RgM3dn3NyPFeUgnZKXEqoCcD5JMxlyijv3vwV0lKtJq7sAEmYQaw23bqubGjrZ3qLk76xU00tNcY3aa3zf6095AsNiNr3VIWg7qyA_fjmujj_xn6I_Kgo7F02OLuMbnjyyfk3rS7qH9KPMpZQxk9h7N48_Lp95LOZ_PPQ05tXdFyVdHh_MuIQ34XJmVNl-gkQgtTYeVyVf7--cu0IXyhJ8iuLrsq3bXSM3K49-nraBx2ER1ClwiVhJLlQBicdIwn3kXWe-YUV2lhc-O9zAueRdIo5bPMi9TigpGkOXPcSS9YbPhzsgNP9y8J9TZztsgAXMoICzh0KvUCtYAyZgUrAqI2b0-7Tu4co24s9dVjj4A0zKLGWdTNLOqLgMR9y9NW8uMWbT42AOkbmLMFusypRB_N9vXkIJoejXZnmgfk_QZBGgwZb2dM6Vf1uvG1kxhdAOq8aKHV98ZYDGRDRAH51mKtL0F18Pagpjt1qBO9rPXa69Mrn311VDiZ5TzWDvivFkJxbXjKdO4MlwUKNrkkILIB3a0HrSf7Y0y9-teGr8l9yGat_-gbslOd1f4tcLzKvmus9w9N9UAT
linkProvider Wiley-Blackwell
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1db9MwFLXQJgEvfDPCZ5AQb6lS27GTx6qwldKWatq0iRfLdhyBVqXTmqDBEz-B38gv4V4nDeu0hwnxFiW2Izvn2se-N-cS8iZ2XAtpskjrFDYoImVRZhJU3RcM2DLMgF54fjoTo0M-Pk6O23RA-C9Mow_RHbihZfj5Gg0cD6QvWTk6JiUXrRSnBH7SA0K57d11yJD2_2pJ8UZ1F5bAJMoAeJthPVe2tLFWbeOwn19FRDuV0U2C61eo3btkse5bE5hy0qsr07M_Lsk-_qfO3yN3WiYbDhro3Sc3XPmA3Jy2vvqHxKGiNTwLv8F23H__8GsZzmfzyYCFpq7CclmFg_mnIYP7baaUVbjAOJGw0BUWLpfl75-_dJPFF1qC29X3tkjrWXpEDnffHwxHUZvUIbIJl0kkaA6cwQpLWeJsbJyjVjKZFibXzom8YFkstJQuyxxPDc4ZSZpTy6xwnPY1e0y24O3uCQmdyawpMsCX1NwAFK1MHUc5oIwaTouAyPXnU7ZVPMfEGwt1cefD4RpGUeEoKj-K6jwg_a7maaP6cY06bz1Cugr67ASj5mSijmZ7arwfT4-G72aKBeT1GkIKbBkdNLp0y3rlw-0EJhiAMjsNtrrWKO0D3-BxQD43YOueoEB4s1dTrUDUF7Wo1cqp0wsnvyourMhy1lcWKLDiXDKlWUpVbjUTBWo22SQgwqPu2p1W470RXj3914qvyK3RwXSiJh9mH5-R21CENuGkz8lWdVa7F0D5KvPSm_IfUeFEMQ
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1bb9MwFLbQJk28cIeFa5AQb6lS27Hjx6qjK2UN1cS0iRfLdhyBWqXVmqDBEz-B38gv4ThOwzrtYUK8WfElsvMd-7N98h2E3sSWKsa1iJRKYYPCUhIJnTjVfUaALcMM2AjPTzM2PqGTs-Ss9X9y_8J4fYjuwM1ZRjNfOwNf5cUVI3f3kpyyVomTAz3pAZ_cpQxWTUeQjv9KSVEvugsrYBIJwN22V8-1LW0tVbtu1C-u46GdyOg2v20WqNFdNN90zfulzHt1pXvmxxXVx__T93voTstjw4EH3n10y5YP0N60val_iKzTs4a88BtsxpuvH34tw1k2OxqQUNdVWC6rcDD7OCTwvI2Tsg4XzkskLFTlCpfL8vfPX8rH8IWW4HH1vS3S3is9Qiejd5-G46gN6RCZhPIkYjgHxmCYwSSxJtbWYsMJTwudK2tZXhARM8W5FcLSVLsZI0lzbIhhluK-Io_RDrzd7qPQamF0IQBdXFENQDQ8tdSJAQmsKS4CxDdfT5pW79yF3VjIy_seCmkYRelGUTajKC8C1O9qrrzmxw3qvG0A0lVQ53PnM8cTeZodyslxPD0dHmSSBOj1BkESLNldz6jSLut142zHXHgBKPPEQ6trDeM-sA0aB-izx1qX4-TB_U5NtvJQX-SilmsrV5fOfWVcGCZy0pcGCLCklBOpSIplbhRhhVNsMkmAWAO6G3daTg7HLvX0Xyu-Qnuzg5E8ep99eIZuQwnsfUmfo53qvLYvgO9V-mVjyH8AOQtC4A
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=Genetic+variation+in+PNPLA3+but+not+APOC3+influences+liver+fat+in+non-alcoholic+fatty+liver+disease&rft.jtitle=Journal+of+gastroenterology+and+hepatology&rft.au=Hyysalo%2C+Jenni&rft.au=Stojkovic%2C+Ivana&rft.au=Kotronen%2C+Anna&rft.au=Hakkarainen%2C+Antti&rft.date=2012-05-01&rft.eissn=1440-1746&rft.volume=27&rft.issue=5&rft.spage=951&rft_id=info:doi/10.1111%2Fj.1440-1746.2011.07045.x&rft_id=info%3Apmid%2F22141340&rft.externalDocID=22141340
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0815-9319&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0815-9319&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0815-9319&client=summon