Serum Angiopoietin-like Protein 6, Risk of Type 2 Diabetes, and Response to Hyperglycemia: A Prospective Cohort Study

Abstract Context Angiopoietin-like protein 6 (ANGPTL6) is a hepatokine that improves insulin sensitivity in animals. However, serum ANGPTL6 concentration was found to be higher in human participants with diabetes or metabolic syndrome in cross-sectional studies, implying that ANGPTL6 may be induced...

Full description

Saved in:
Bibliographic Details
Published inThe journal of clinical endocrinology and metabolism Vol. 105; no. 5; pp. e1949 - e1957
Main Authors Fan, Kang-Chih, Wu, Hung-Tsung, Wei, Jung-Nan, Chuang, Lee-Ming, Hsu, Chih-Yao, Yen, I-Weng, Lin, Chia-Hung, Lin, Mao-Shin, Shih, Shyang-Rong, Wang, Shu-Huei, Chang, Tien-Jyun, Li, Hung-Yuan
Format Journal Article
LanguageEnglish
Published US Oxford University Press 01.05.2020
Copyright Oxford University Press
Subjects
Online AccessGet full text
ISSN0021-972X
1945-7197
1945-7197
DOI10.1210/clinem/dgaa103

Cover

Abstract Abstract Context Angiopoietin-like protein 6 (ANGPTL6) is a hepatokine that improves insulin sensitivity in animals. However, serum ANGPTL6 concentration was found to be higher in human participants with diabetes or metabolic syndrome in cross-sectional studies, implying that ANGPTL6 may be induced to counteract hyperglycemia. Objective To investigate whether serum ANGPTL6 can predict incident diabetes and explore whether glucose or insulin can regulate ANGPTL6 expression and secretion. Design This cohort study included adults without diabetes at baseline who were followed every 2 years for incident diabetes. Serum ANGPTL6 concentrations were measured at baseline and during oral glucose tolerance tests (OGTTs). A hepatic cell line, HepG2, and diet-induced obesity mouse model were used to evaluate the response of ANGPTL6 expression and secretion to hyperglycemia and the metabolic syndrome. Results We recruited 1103 participants without diabetes at baseline. During the 4.22-year follow-up, 113 (10.2%) participants developed incident diabetes. Serum ANGPTL6 was negatively associated with the incidence of diabetes (adjusted hazard ratio, 0.77; P = 0.042). However, serum ANGPTL6 level was higher in participants with prediabetes (P = 0.018) and was elevated during OGTT. In HepG2 cells, treatment with glucose, but not insulin, induced ANGPTL6 expression. Hepatic ANGPTL6 expression and serum ANGPTL6 concentrations were significantly higher in mice fed with a high-fat diet than in those fed with a standard chow (both P < 0.05). Conclusion A high serum ANGPTL6 level is associated with a low incidence of diabetes in humans. ANGPTL6 is expressed and secreted in response to hyperglycemia to maintain glucose homeostasis.
AbstractList Abstract Context Angiopoietin-like protein 6 (ANGPTL6) is a hepatokine that improves insulin sensitivity in animals. However, serum ANGPTL6 concentration was found to be higher in human participants with diabetes or metabolic syndrome in cross-sectional studies, implying that ANGPTL6 may be induced to counteract hyperglycemia. Objective To investigate whether serum ANGPTL6 can predict incident diabetes and explore whether glucose or insulin can regulate ANGPTL6 expression and secretion. Design This cohort study included adults without diabetes at baseline who were followed every 2 years for incident diabetes. Serum ANGPTL6 concentrations were measured at baseline and during oral glucose tolerance tests (OGTTs). A hepatic cell line, HepG2, and diet-induced obesity mouse model were used to evaluate the response of ANGPTL6 expression and secretion to hyperglycemia and the metabolic syndrome. Results We recruited 1103 participants without diabetes at baseline. During the 4.22-year follow-up, 113 (10.2%) participants developed incident diabetes. Serum ANGPTL6 was negatively associated with the incidence of diabetes (adjusted hazard ratio, 0.77; P = 0.042). However, serum ANGPTL6 level was higher in participants with prediabetes (P = 0.018) and was elevated during OGTT. In HepG2 cells, treatment with glucose, but not insulin, induced ANGPTL6 expression. Hepatic ANGPTL6 expression and serum ANGPTL6 concentrations were significantly higher in mice fed with a high-fat diet than in those fed with a standard chow (both P < 0.05). Conclusion A high serum ANGPTL6 level is associated with a low incidence of diabetes in humans. ANGPTL6 is expressed and secreted in response to hyperglycemia to maintain glucose homeostasis.
Context Angiopoietin-like protein 6 (ANGPTL6) is a hepatokine that improves insulin sensitivity in animals. However, serum ANGPTL6 concentration was found to be higher in human participants with diabetes or metabolic syndrome in cross-sectional studies, implying that ANGPTL6 may be induced to counteract hyperglycemia. Objective To investigate whether serum ANGPTL6 can predict incident diabetes and explore whether glucose or insulin can regulate ANGPTL6 expression and secretion. Design This cohort study included adults without diabetes at baseline who were followed every 2 years for incident diabetes. Serum ANGPTL6 concentrations were measured at baseline and during oral glucose tolerance tests (OGTTs). A hepatic cell line, HepG2, and diet-induced obesity mouse model were used to evaluate the response of ANGPTL6 expression and secretion to hyperglycemia and the metabolic syndrome. Results We recruited 1103 participants without diabetes at baseline. During the 4.22-year follow-up, 113 (10.2%) participants developed incident diabetes. Serum ANGPTL6 was negatively associated with the incidence of diabetes (adjusted hazard ratio, 0.77; P = 0.042). However, serum ANGPTL6 level was higher in participants with prediabetes (P = 0.018) and was elevated during OGTT. In HepG2 cells, treatment with glucose, but not insulin, induced ANGPTL6 expression. Hepatic ANGPTL6 expression and serum ANGPTL6 concentrations were significantly higher in mice fed with a high-fat diet than in those fed with a standard chow (both P < 0.05). Conclusion A high serum ANGPTL6 level is associated with a low incidence of diabetes in humans. ANGPTL6 is expressed and secreted in response to hyperglycemia to maintain glucose homeostasis.
Angiopoietin-like protein 6 (ANGPTL6) is a hepatokine that improves insulin sensitivity in animals. However, serum ANGPTL6 concentration was found to be higher in human participants with diabetes or metabolic syndrome in cross-sectional studies, implying that ANGPTL6 may be induced to counteract hyperglycemia. To investigate whether serum ANGPTL6 can predict incident diabetes and explore whether glucose or insulin can regulate ANGPTL6 expression and secretion. This cohort study included adults without diabetes at baseline who were followed every 2 years for incident diabetes. Serum ANGPTL6 concentrations were measured at baseline and during oral glucose tolerance tests (OGTTs). A hepatic cell line, HepG2, and diet-induced obesity mouse model were used to evaluate the response of ANGPTL6 expression and secretion to hyperglycemia and the metabolic syndrome. We recruited 1103 participants without diabetes at baseline. During the 4.22-year follow-up, 113 (10.2%) participants developed incident diabetes. Serum ANGPTL6 was negatively associated with the incidence of diabetes (adjusted hazard ratio, 0.77; P = 0.042). However, serum ANGPTL6 level was higher in participants with prediabetes (P = 0.018) and was elevated during OGTT. In HepG2 cells, treatment with glucose, but not insulin, induced ANGPTL6 expression. Hepatic ANGPTL6 expression and serum ANGPTL6 concentrations were significantly higher in mice fed with a high-fat diet than in those fed with a standard chow (both P < 0.05). A high serum ANGPTL6 level is associated with a low incidence of diabetes in humans. ANGPTL6 is expressed and secreted in response to hyperglycemia to maintain glucose homeostasis.
Angiopoietin-like protein 6 (ANGPTL6) is a hepatokine that improves insulin sensitivity in animals. However, serum ANGPTL6 concentration was found to be higher in human participants with diabetes or metabolic syndrome in cross-sectional studies, implying that ANGPTL6 may be induced to counteract hyperglycemia.CONTEXTAngiopoietin-like protein 6 (ANGPTL6) is a hepatokine that improves insulin sensitivity in animals. However, serum ANGPTL6 concentration was found to be higher in human participants with diabetes or metabolic syndrome in cross-sectional studies, implying that ANGPTL6 may be induced to counteract hyperglycemia.To investigate whether serum ANGPTL6 can predict incident diabetes and explore whether glucose or insulin can regulate ANGPTL6 expression and secretion.OBJECTIVETo investigate whether serum ANGPTL6 can predict incident diabetes and explore whether glucose or insulin can regulate ANGPTL6 expression and secretion.This cohort study included adults without diabetes at baseline who were followed every 2 years for incident diabetes. Serum ANGPTL6 concentrations were measured at baseline and during oral glucose tolerance tests (OGTTs). A hepatic cell line, HepG2, and diet-induced obesity mouse model were used to evaluate the response of ANGPTL6 expression and secretion to hyperglycemia and the metabolic syndrome.DESIGNThis cohort study included adults without diabetes at baseline who were followed every 2 years for incident diabetes. Serum ANGPTL6 concentrations were measured at baseline and during oral glucose tolerance tests (OGTTs). A hepatic cell line, HepG2, and diet-induced obesity mouse model were used to evaluate the response of ANGPTL6 expression and secretion to hyperglycemia and the metabolic syndrome.We recruited 1103 participants without diabetes at baseline. During the 4.22-year follow-up, 113 (10.2%) participants developed incident diabetes. Serum ANGPTL6 was negatively associated with the incidence of diabetes (adjusted hazard ratio, 0.77; P = 0.042). However, serum ANGPTL6 level was higher in participants with prediabetes (P = 0.018) and was elevated during OGTT. In HepG2 cells, treatment with glucose, but not insulin, induced ANGPTL6 expression. Hepatic ANGPTL6 expression and serum ANGPTL6 concentrations were significantly higher in mice fed with a high-fat diet than in those fed with a standard chow (both P < 0.05).RESULTSWe recruited 1103 participants without diabetes at baseline. During the 4.22-year follow-up, 113 (10.2%) participants developed incident diabetes. Serum ANGPTL6 was negatively associated with the incidence of diabetes (adjusted hazard ratio, 0.77; P = 0.042). However, serum ANGPTL6 level was higher in participants with prediabetes (P = 0.018) and was elevated during OGTT. In HepG2 cells, treatment with glucose, but not insulin, induced ANGPTL6 expression. Hepatic ANGPTL6 expression and serum ANGPTL6 concentrations were significantly higher in mice fed with a high-fat diet than in those fed with a standard chow (both P < 0.05).A high serum ANGPTL6 level is associated with a low incidence of diabetes in humans. ANGPTL6 is expressed and secreted in response to hyperglycemia to maintain glucose homeostasis.CONCLUSIONA high serum ANGPTL6 level is associated with a low incidence of diabetes in humans. ANGPTL6 is expressed and secreted in response to hyperglycemia to maintain glucose homeostasis.
Author Hsu, Chih-Yao
Yen, I-Weng
Li, Hung-Yuan
Chuang, Lee-Ming
Lin, Mao-Shin
Lin, Chia-Hung
Shih, Shyang-Rong
Chang, Tien-Jyun
Wu, Hung-Tsung
Wang, Shu-Huei
Fan, Kang-Chih
Wei, Jung-Nan
AuthorAffiliation Division of Endocrinology and Metabolism, Department of Internal Medicine, National, Taiwan University Hospital Hsinchu Branch, Hsinchu, Taiwan Graduate Institute of Clinical Medicine, College of Medicine, National Taiwan University, Taipei, Taiwan Graduate Institute of Metabolism and Obesity Sciences, College of Nutrition, Taipei, Medical University, Taipei, Taiwan Chia Nan University of Pharmacy and Science, Tainan, Taiwan Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan Department of Anatomy and Cell Biology, National Taiwan University, Taipei, Taiwan
AuthorAffiliation_xml – name: Division of Endocrinology and Metabolism, Department of Internal Medicine, National, Taiwan University Hospital Hsinchu Branch, Hsinchu, Taiwan Graduate Institute of Clinical Medicine, College of Medicine, National Taiwan University, Taipei, Taiwan Graduate Institute of Metabolism and Obesity Sciences, College of Nutrition, Taipei, Medical University, Taipei, Taiwan Chia Nan University of Pharmacy and Science, Tainan, Taiwan Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan Department of Anatomy and Cell Biology, National Taiwan University, Taipei, Taiwan
Author_xml – sequence: 1
  givenname: Kang-Chih
  surname: Fan
  fullname: Fan, Kang-Chih
  organization: Division of Endocrinology and Metabolism, Department of Internal Medicine, National Taiwan University Hospital Hsinchu Branch, Hsinchu, Taiwan
– sequence: 2
  givenname: Hung-Tsung
  surname: Wu
  fullname: Wu, Hung-Tsung
  organization: Graduate Institute of Metabolism and Obesity Sciences, College of Nutrition, Taipei Medical University, Taipei, Taiwan
– sequence: 3
  givenname: Jung-Nan
  surname: Wei
  fullname: Wei, Jung-Nan
  organization: Chia Nan University of Pharmacy and Science, Tainan, Taiwan
– sequence: 4
  givenname: Lee-Ming
  surname: Chuang
  fullname: Chuang, Lee-Ming
  organization: Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan
– sequence: 5
  givenname: Chih-Yao
  surname: Hsu
  fullname: Hsu, Chih-Yao
  organization: Division of Endocrinology and Metabolism, Department of Internal Medicine, National Taiwan University Hospital Hsinchu Branch, Hsinchu, Taiwan
– sequence: 6
  givenname: I-Weng
  surname: Yen
  fullname: Yen, I-Weng
  organization: Division of Endocrinology and Metabolism, Department of Internal Medicine, National Taiwan University Hospital Hsinchu Branch, Hsinchu, Taiwan
– sequence: 7
  givenname: Chia-Hung
  surname: Lin
  fullname: Lin, Chia-Hung
  organization: Division of Endocrinology and Metabolism, Department of Internal Medicine, National Taiwan University Hospital Hsinchu Branch, Hsinchu, Taiwan
– sequence: 8
  givenname: Mao-Shin
  surname: Lin
  fullname: Lin, Mao-Shin
  organization: Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan
– sequence: 9
  givenname: Shyang-Rong
  orcidid: 0000-0001-7424-1358
  surname: Shih
  fullname: Shih, Shyang-Rong
  organization: Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan
– sequence: 10
  givenname: Shu-Huei
  surname: Wang
  fullname: Wang, Shu-Huei
  organization: Graduate Institute of Anatomy and Cell Biology, College of Medicine, National Taiwan University, Taipei, Taiwan
– sequence: 11
  givenname: Tien-Jyun
  surname: Chang
  fullname: Chang, Tien-Jyun
  email: tjc922@gmail.com
  organization: Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan
– sequence: 12
  givenname: Hung-Yuan
  orcidid: 0000-0001-9644-2855
  surname: Li
  fullname: Li, Hung-Yuan
  email: larsli@ntuh.gov.tw
  organization: Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan
BackLink https://www.ncbi.nlm.nih.gov/pubmed/32123920$$D View this record in MEDLINE/PubMed
BookMark eNqFkU1v1DAQhi1URLeFK0dkiQtITevPuOG2WgpFqgRqi8QtcpzJrruOHWyHav99U2XhUKniNJfneTUz7xE68MEDQm8pOaWMkjPjrIf-rF1rTQl_gRa0ErJQtFIHaEEIo0Wl2K9DdJTSHSFUCMlfoUPOKOMVIws03kAce7z0axuGYCFbXzi7BfwjhgzW4_IEX9u0xaHDt7sBMMOfrW4gQzrB2rf4GtIQfAKcA76cgLh2OwO91Z_w8jEkDWCy_QN4FTYhZnyTx3b3Gr3stEvwZj-P0c8vF7ery-Lq-9dvq-VVYURZ8gJkC5Ib4CA6I0vTcCWaljWkVEoaTkAKQ41qzyuudMuF4NoYzs41Y6qTUvBj9GHOHWL4PULKdW-TAee0hzCmmnFFRCVpKSf0_RP0LozRT9vVTPDpt1xINlHv9tTY9NDWQ7S9jrv670Mn4HQGzHR6itD9QyipHxur58bqfWOTIJ4IxmadbfA5auue19is3QeXIaatG-8h1hvQLm-elz7OUhiH_-31ANL7u78
CitedBy_id crossref_primary_10_1016_j_cjca_2023_06_002
crossref_primary_10_2169_internalmedicine_3609_24
crossref_primary_10_3389_fmolb_2022_909151
crossref_primary_10_1016_j_molmet_2020_101138
crossref_primary_10_1111_jdi_14311
crossref_primary_10_1210_clinem_dgaa103
crossref_primary_10_1210_clinem_dgac414
crossref_primary_10_1007_s00592_024_02335_9
crossref_primary_10_3390_jcm11185477
Cites_doi 10.1016/j.jhep.2006.01.010
10.1210/jc.2018-01828
10.1007/s001250100580
10.2337/dc12-1452
10.1016/j.metabol.2008.11.016
10.1016/j.molmet.2014.05.005
10.2337/dc10-0646
10.1016/j.metabol.2010.05.013
10.1016/j.cmet.2009.08.003
10.1055/s-0034-1382078
10.1194/jlr.M500005-JLR200
10.2337/dc12-0166
10.1016/j.tcm.2007.10.003
10.2337/diacare.21.12.2191
10.2337/dc08-1478
10.1210/clinem/dgaa103
10.1038/srep39777
10.2337/dc19-S002
10.3389/fendo.2014.00004
10.1002/dme.1996.13.s6.109
10.1111/j.1742-4658.2010.07979.x
10.1111/j.1365-2265.2011.04129.x
10.1038/nm1214
10.1016/j.molmed.2005.08.002
ContentType Journal Article
Copyright Endocrine Society 2020. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com 2020
Copyright © Oxford University Press 2015
Endocrine Society 2020. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.
Copyright_xml – notice: Endocrine Society 2020. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com 2020
– notice: Copyright © Oxford University Press 2015
– notice: Endocrine Society 2020. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.
DBID AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
3V.
7QP
7T5
7TM
7X7
7XB
88E
8FI
8FJ
8FK
ABUWG
AFKRA
BENPR
CCPQU
FYUFA
GHDGH
H94
K9.
M0S
M1P
PHGZM
PHGZT
PJZUB
PKEHL
PPXIY
PQEST
PQQKQ
PQUKI
7X8
DOI 10.1210/clinem/dgaa103
DatabaseName CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
ProQuest Central (Corporate)
Calcium & Calcified Tissue Abstracts
Immunology Abstracts
Nucleic Acids Abstracts
Health & Medical Collection
ProQuest Central (purchase pre-March 2016)
Medical Database (Alumni Edition)
Hospital Premium Collection
Hospital Premium Collection (Alumni Edition)
ProQuest Central (Alumni) (purchase pre-March 2016)
ProQuest Central (Alumni)
ProQuest Central UK/Ireland
ProQuest Central
ProQuest One Community College
Health Research Premium Collection (UHCL Subscription)
Health Research Premium Collection (Alumni)
AIDS and Cancer Research Abstracts
ProQuest Health & Medical Complete (Alumni)
ProQuest Health & Medical Collection
Medical Database
Proquest Central Premium
ProQuest One Academic (New)
ProQuest Health & Medical Research Collection
ProQuest One Academic Middle East (New)
ProQuest One Health & Nursing
ProQuest One Academic Eastern Edition (DO NOT USE)
ProQuest One Academic
ProQuest One Academic UKI Edition
MEDLINE - Academic
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
ProQuest One Academic Middle East (New)
Nucleic Acids Abstracts
ProQuest Health & Medical Complete (Alumni)
ProQuest Central (Alumni Edition)
ProQuest One Community College
ProQuest One Health & Nursing
ProQuest Central
ProQuest Health & Medical Research Collection
Health Research Premium Collection
Health and Medicine Complete (Alumni Edition)
Health & Medical Research Collection
AIDS and Cancer Research Abstracts
ProQuest Central (New)
ProQuest Medical Library (Alumni)
ProQuest One Academic Eastern Edition
ProQuest Hospital Collection
Health Research Premium Collection (Alumni)
ProQuest Hospital Collection (Alumni)
ProQuest Health & Medical Complete
ProQuest Medical Library
ProQuest One Academic UKI Edition
Immunology Abstracts
ProQuest One Academic
Calcium & Calcified Tissue Abstracts
ProQuest One Academic (New)
ProQuest Central (Alumni)
MEDLINE - Academic
DatabaseTitleList
ProQuest One Academic Middle East (New)
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
– sequence: 3
  dbid: BENPR
  name: ProQuest Central
  url: http://www.proquest.com/pqcentral?accountid=15518
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 1945-7197
EndPage e1957
ExternalDocumentID 32123920
10_1210_clinem_dgaa103
10.1210/clinem/dgaa103
Genre Research Support, Non-U.S. Gov't
Journal Article
GeographicLocations Taiwan
GeographicLocations_xml – name: Taiwan
GroupedDBID ---
-~X
.55
.GJ
.XZ
08P
0R~
18M
1TH
29K
2WC
34G
354
39C
3O-
3V.
4.4
48X
53G
5GY
5RS
5YH
8F7
AABZA
AACZT
AAIMJ
AAJQQ
AAKAS
AAPGJ
AAPQZ
AAPXW
AAQQT
AARHZ
AAUAY
AAUQX
AAVAP
AAWDT
AAWTL
AAYJJ
ABBLC
ABJNI
ABLJU
ABMNT
ABNHQ
ABOCM
ABPMR
ABPPZ
ABPQP
ABPTD
ABQNK
ABSAR
ABWST
ABXVV
ACFRR
ACGFO
ACGFS
ACPRK
ACUTJ
ACYHN
ACZBC
ADBBV
ADGKP
ADGZP
ADHKW
ADQBN
ADRTK
ADVEK
ADZCM
AELWJ
AEMDU
AENEX
AENZO
AERZD
AETBJ
AEWNT
AFCHL
AFFNX
AFFZL
AFGWE
AFOFC
AFRAH
AFXAL
AFYAG
AGINJ
AGKRT
AGMDO
AGQXC
AGUTN
AHMBA
AI.
AJEEA
ALMA_UNASSIGNED_HOLDINGS
APIBT
APJGH
AQDSO
AQKUS
ARIXL
ASPBG
ATGXG
AVNTJ
AVWKF
AZFZN
BAWUL
BAYMD
BCRHZ
BENPR
BEYMZ
BPHCQ
BSWAC
BTRTY
BVXVI
C45
CDBKE
CS3
D-I
DAKXR
DIK
E3Z
EBS
EIHJH
EJD
EMOBN
ENERS
F5P
FECEO
FEDTE
FHSFR
FLUFQ
FOEOM
FOTVD
FQBLK
G8K
GAUVT
GJXCC
GX1
H13
HVGLF
HZ~
H~9
IAO
IHR
INH
J5H
KBUDW
KOP
KQ8
KSI
KSN
L7B
M5~
MBLQV
MHKGH
MJL
N4W
N9A
NLBLG
NOMLY
NOYVH
NVLIB
O9-
OAUYM
OBH
OCB
ODMLO
OFXIZ
OGEVE
OHH
OJZSN
OK1
OPAEJ
OVD
OVIDX
P2P
P6G
PQQKQ
PROAC
REU
ROX
ROZ
TEORI
TJX
TLC
TMA
TR2
TWZ
VH1
VVN
W8F
WHG
WOQ
X52
X7M
YBU
YFH
YHG
YOC
YSK
ZGI
ZXP
ZY1
~02
~H1
7X7
88E
8FI
8FJ
ABDFA
ABEJV
ABGNP
ABUWG
ABVGC
ABXZS
ADNBA
AEMQT
AEOTA
AFKRA
AGORE
AHGBF
AHMMS
AJBYB
ALXQX
CCPQU
FYUFA
HMCUK
ITC
M1P
NU-
PHGZM
PHGZT
PSQYO
UKHRP
AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
PJZUB
PPXIY
7QP
7T5
7TM
7XB
8FK
AEHZK
H94
K9.
PKEHL
PQEST
PQUKI
PUEGO
7X8
ID FETCH-LOGICAL-c4663-e5de53ce3e4fc56cb374bd2b06775c30e54c1c7d8937ad3443acc328a227f5543
IEDL.DBID 7X7
ISSN 0021-972X
1945-7197
IngestDate Sat Sep 27 16:37:24 EDT 2025
Fri Sep 19 20:51:43 EDT 2025
Mon Jul 21 06:08:38 EDT 2025
Tue Jul 01 01:10:55 EDT 2025
Thu Apr 24 23:08:49 EDT 2025
Fri May 16 03:53:32 EDT 2025
Wed Aug 28 03:18:40 EDT 2024
IsPeerReviewed true
IsScholarly true
Issue 5
Keywords hyperglycemia
angiopoietin-like protein 6
biomarker
diabetes
Language English
License This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model)
https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model
Endocrine Society 2020. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c4663-e5de53ce3e4fc56cb374bd2b06775c30e54c1c7d8937ad3443acc328a227f5543
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ORCID 0000-0001-7424-1358
0000-0001-9644-2855
PMID 32123920
PQID 2431033452
PQPubID 2046206
ParticipantIDs proquest_miscellaneous_2370495165
proquest_journals_2431033452
pubmed_primary_32123920
crossref_primary_10_1210_clinem_dgaa103
crossref_citationtrail_10_1210_clinem_dgaa103
wolterskluwer_health_10_1210_clinem_dgaa103
oup_primary_10_1210_clinem_dgaa103
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2020-05-01
PublicationDateYYYYMMDD 2020-05-01
PublicationDate_xml – month: 05
  year: 2020
  text: 2020-05-01
  day: 01
PublicationDecade 2020
PublicationPlace US
PublicationPlace_xml – name: US
– name: United States
– name: Washington
PublicationTitle The journal of clinical endocrinology and metabolism
PublicationTitleAlternate J Clin Endocrinol Metab
PublicationYear 2020
Publisher Oxford University Press
Copyright Oxford University Press
Publisher_xml – name: Oxford University Press
– name: Copyright Oxford University Press
References Tabata (2020051909382899000_CIT0004) 2009; 10
Ge (2020051909382899000_CIT0003) 2005; 46
Hato (2020051909382899000_CIT0008) 2008; 18
DeFronzo (2020051909382899000_CIT0021) 2010; 33
Kadomatsu (2020051909382899000_CIT0007) 2011; 278
Santulli (2020051909382899000_CIT0019) 2014; 5
Ebert (2020051909382899000_CIT0010) 2014; 46
George (2020051909382899000_CIT0018) 2006; 44
Pratley (2020051909382899000_CIT0022) 2001; 44
Doi (2020051909382899000_CIT0006) 2013; 36
Association AD (2020051909382899000_CIT0016) 2019; 42
Oike (2020051909382899000_CIT0005) 2005; 11
Ebert (2020051909382899000_CIT0009) 2009; 58
Fan (2020051909382899000_CIT0017) 2020
Peddinti (2020051909382899000_CIT0020) 2019; 104
Oike (2020051909382899000_CIT0002) 2005; 11
Namkung (2020051909382899000_CIT0011) 2011; 60
Hung (2020051909382899000_CIT0013) 2011; 75
Yu (2020051909382899000_CIT0014) 2017; 7
Ma (2020051909382899000_CIT0012) 2013; 36
Levy (2020051909382899000_CIT0015) 1998; 21
Kosaka (2020051909382899000_CIT0023) 1996; 13
Abdul-Wahed (2020051909382899000_CIT0001) 2014; 3
Utzschneider (2020051909382899000_CIT0024) 2009; 32
References_xml – volume: 44
  start-page: 832
  issue: 4
  year: 2006
  ident: 2020051909382899000_CIT0018
  article-title: Angiopoietin-like proteins: another player in the metabolic field
  publication-title: J Hepatol.
  doi: 10.1016/j.jhep.2006.01.010
– volume: 104
  start-page: 1131
  issue: 4
  year: 2019
  ident: 2020051909382899000_CIT0020
  article-title: 1-hour post-OGTT glucose improves the early prediction of type 2 diabetes by clinical and metabolic markers
  publication-title: J Clin Endocrinol Metab.
  doi: 10.1210/jc.2018-01828
– volume: 44
  start-page: 929
  issue: 8
  year: 2001
  ident: 2020051909382899000_CIT0022
  article-title: The role of impaired early insulin secretion in the pathogenesis of type II diabetes mellitus
  publication-title: Diabetologia.
  doi: 10.1007/s001250100580
– volume: 36
  start-page: 1660
  issue: 6
  year: 2013
  ident: 2020051909382899000_CIT0012
  article-title: Measurement of waist circumference: midabdominal or iliac crest?
  publication-title: Diabetes Care.
  doi: 10.2337/dc12-1452
– volume: 58
  start-page: 547
  issue: 4
  year: 2009
  ident: 2020051909382899000_CIT0009
  article-title: Serum levels of angiopoietin-related growth factor in diabetes mellitus and chronic hemodialysis
  publication-title: Metabolism.
  doi: 10.1016/j.metabol.2008.11.016
– volume: 3
  start-page: 531
  issue: 5
  year: 2014
  ident: 2020051909382899000_CIT0001
  article-title: A link between hepatic glucose production and peripheral energy metabolism via hepatokines
  publication-title: Mol Metab.
  doi: 10.1016/j.molmet.2014.05.005
– volume: 33
  start-page: e93
  issue: 7
  year: 2010
  ident: 2020051909382899000_CIT0021
  article-title: Reduced time points to calculate the composite index
  publication-title: Diabetes Care.
  doi: 10.2337/dc10-0646
– volume: 60
  start-page: 564
  issue: 4
  year: 2011
  ident: 2020051909382899000_CIT0011
  article-title: Serum levels of angiopoietin-related growth factor are increased in metabolic syndrome
  publication-title: Metabolism.
  doi: 10.1016/j.metabol.2010.05.013
– volume: 10
  start-page: 178
  issue: 3
  year: 2009
  ident: 2020051909382899000_CIT0004
  article-title: Angiopoietin-like protein 2 promotes chronic adipose tissue inflammation and obesity-related systemic insulin resistance
  publication-title: Cell Metab.
  doi: 10.1016/j.cmet.2009.08.003
– volume: 46
  start-page: 685
  issue: 10
  year: 2014
  ident: 2020051909382899000_CIT0010
  article-title: Relationship between serum levels of angiopoietin-related growth factor and metabolic risk factors
  publication-title: Horm Metab Res.
  doi: 10.1055/s-0034-1382078
– volume: 46
  start-page: 1484
  issue: 7
  year: 2005
  ident: 2020051909382899000_CIT0003
  article-title: Differential regulation and properties of angiopoietin-like proteins 3 and 4
  publication-title: J Lipid Res.
  doi: 10.1194/jlr.M500005-JLR200
– volume: 36
  start-page: 98
  issue: 1
  year: 2013
  ident: 2020051909382899000_CIT0006
  article-title: Angiopoietin-like protein 2 and risk of type 2 diabetes in a general Japanese population: the Hisayama study
  publication-title: Diabetes Care.
  doi: 10.2337/dc12-0166
– volume: 18
  start-page: 6
  issue: 1
  year: 2008
  ident: 2020051909382899000_CIT0008
  article-title: The role of angiopoietin-like proteins in angiogenesis and metabolism
  publication-title: Trends Cardiovasc Med.
  doi: 10.1016/j.tcm.2007.10.003
– volume: 21
  start-page: 2191
  issue: 12
  year: 1998
  ident: 2020051909382899000_CIT0015
  article-title: Correct homeostasis model assessment (HOMA) evaluation uses the computer program
  publication-title: Diabetes Care.
  doi: 10.2337/diacare.21.12.2191
– volume: 32
  start-page: 335
  issue: 2
  year: 2009
  ident: 2020051909382899000_CIT0024
  article-title: Oral disposition index predicts the development of future diabetes above and beyond fasting and 2-h glucose levels
  publication-title: Diabetes Care.
  doi: 10.2337/dc08-1478
– year: 2020
  ident: 2020051909382899000_CIT0017
  article-title: Serum angiopoietin-like protein 6, risk of type 2 diabetes, and response to hyperglycemia: a prospective cohort study. Supplementary tables
  doi: 10.1210/clinem/dgaa103
– volume: 7
  start-page: 39777
  year: 2017
  ident: 2020051909382899000_CIT0014
  article-title: The impact of gastric atrophy on the incidence of diabetes
  publication-title: Sci Rep.
  doi: 10.1038/srep39777
– volume: 42
  start-page: S13
  year: 2019
  ident: 2020051909382899000_CIT0016
  article-title: 2. Classification and diagnosis of diabetes: standards of medical care in diabetes—2019
  publication-title: Diabetes Care.
  doi: 10.2337/dc19-S002
– volume: 5
  start-page: 4
  year: 2014
  ident: 2020051909382899000_CIT0019
  article-title: Angiopoietin-like proteins: a comprehensive look
  publication-title: Front Endocrinol (Lausanne).
  doi: 10.3389/fendo.2014.00004
– volume: 13
  start-page: S109
  issue: 9 Suppl 6
  year: 1996
  ident: 2020051909382899000_CIT0023
  article-title: Insulin response to oral glucose load is consistently decreased in established non-insulin-dependent diabetes mellitus: the usefulness of decreased early insulin response as a predictor of non-insulin-dependent diabetes mellitus
  publication-title: Diabet Med.
  doi: 10.1002/dme.1996.13.s6.109
– volume: 278
  start-page: 559
  issue: 4
  year: 2011
  ident: 2020051909382899000_CIT0007
  article-title: Angiopoietin-like proteins: emerging targets for treatment of obesity and related metabolic diseases
  publication-title: FEBS J.
  doi: 10.1111/j.1742-4658.2010.07979.x
– volume: 75
  start-page: 780
  issue: 6
  year: 2011
  ident: 2020051909382899000_CIT0013
  article-title: Haemoglobin A1c is associated with carotid intima-media thickness in a Chinese population
  publication-title: Clin Endocrinol (Oxf).
  doi: 10.1111/j.1365-2265.2011.04129.x
– volume: 11
  start-page: 400
  issue: 4
  year: 2005
  ident: 2020051909382899000_CIT0005
  article-title: Angiopoietin-related growth factor antagonizes obesity and insulin resistance
  publication-title: Nat Med.
  doi: 10.1038/nm1214
– volume: 11
  start-page: 473
  issue: 10
  year: 2005
  ident: 2020051909382899000_CIT0002
  article-title: Angiopoietin-like proteins: potential new targets for metabolic syndrome therapy
  publication-title: Trends Mol Med.
  doi: 10.1016/j.molmed.2005.08.002
SSID ssj0014453
Score 2.398247
Snippet Abstract Context Angiopoietin-like protein 6 (ANGPTL6) is a hepatokine that improves insulin sensitivity in animals. However, serum ANGPTL6 concentration was...
Angiopoietin-like protein 6 (ANGPTL6) is a hepatokine that improves insulin sensitivity in animals. However, serum ANGPTL6 concentration was found to be higher...
Context Angiopoietin-like protein 6 (ANGPTL6) is a hepatokine that improves insulin sensitivity in animals. However, serum ANGPTL6 concentration was found to...
SourceID proquest
pubmed
crossref
wolterskluwer
oup
SourceType Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage e1949
SubjectTerms Adult
Angiopoietin
Angiopoietin-like Proteins - blood
Animals
Cohort analysis
Cohort Studies
Cross-sectional studies
Diabetes
Diabetes mellitus (non-insulin dependent)
Diabetes Mellitus, Type 2 - blood
Diabetes Mellitus, Type 2 - epidemiology
Diabetes Mellitus, Type 2 - etiology
Female
Follow-Up Studies
Glucose
Glucose tolerance
Hep G2 Cells
High fat diet
Homeostasis
Humans
Hyperglycemia
Hyperglycemia - blood
Hyperglycemia - epidemiology
Incidence
Insulin
Liver
Male
Metabolic syndrome
Mice
Mice, Inbred C57BL
Middle Aged
Prediabetic State - blood
Prediabetic State - epidemiology
Prospective Studies
Risk Factors
Secretion
Taiwan - epidemiology
Title Serum Angiopoietin-like Protein 6, Risk of Type 2 Diabetes, and Response to Hyperglycemia: A Prospective Cohort Study
URI https://www.ncbi.nlm.nih.gov/pubmed/32123920
https://www.proquest.com/docview/2431033452
https://www.proquest.com/docview/2370495165
Volume 105
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwhV1bb9MwFLZgkxAIIe4UxmQQEg_MWupLkvKCythUQJumikl9ixxfStQuLksrtH_POY1TtofBY5QTx8k5tr9zJ-SdFXliuPbMD0TKpMg907lKWGIQDQxs7jUa9I9P0tGZ_DZRk2hwa2JYZbcnrjdqGwzayPe5xI5YQir-afGLYdco9K7GFhq3yXYfkAi2bsgmG4ULdIVYhRLDEDI-iUUbMWsF8w4djD7Vut81zIqH0rVEtyt48x65_zugC7uZrSPYr5xDRw_Jgwgg6bDl-CNyy9WPyZ3j6CJ_Qlaw-lfndFhPq7AIFWY0s3k1c_QUKzJUNU336LhqZjR4ikoo5TRGxTR7VNeWjtuoWUeXgY6A4GI6vzTuvNIf6RAH6XIz6UH4CdidYiTi5VNydnT442DEYm8FZiSADOaUdUoYJ5z0RqWmFJksLS-xoJwyInFKmr7JLMIZbYWUQhsjeK45zzxAEPGMbNWhdi8IdbAPWKcHygEc0z7XoJJ6n5TwOIyUJT3Cup9bmFh4HPtfzAtUQIAZRcuMIjKjR95v6BdtyY0bKd8Cr_5LtNOxsojrsyn-SlOPvNnchpWF7hJdu7ACGpg7qI_9VPXI81YENq8SeOIPOHzbh2syUbTZqzdM5eW_p_KK3OWoza_DKXfI1vJi5V4D5FmWu2u53iXbnw9PTsdw9eXr9z9OXwPF
linkProvider ProQuest
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtR3ZbtNAcFRSiUMIcRQIFFgQiAdq4eyujyBVKJRWKW2iKmqlvLnr9TpYSe1QJ6ryc3wbM_E6tA-Fpz57vNfMzrFzAbxPROhqrlInbQvfkSJMHRV6ruNq0gbaSZgqetDv9f3uifwx9IZr8LvOhaGwyponLhl1Umh6I__MJXXEEtLjX6e_HOoaRd7VuoWGsq0Vku1liTGb2HFgFhdowpXb-98R3x8439s93uk6tsuAoyWKW8d4ifGENsLIVHu-jkUg44THVFrN08I1ntQtHSQk2FUipBQ4meCh4jxIURgLHPcWrEt6QGnA-rfd_tFg5ceQ0tbBpECIgA9t2UjKm6HMR4P7GynVqlt2WbF4JdXuksZ7D-5fFOREL8fLGPpLknDvITywKizrVDT3CNZM_hhu96yT_gnMkf_Mz1gnH2XFtMgop9qZZGPDjqgmRJYzf4sNsnLMipSRGcw4s3E55RZTecIGVdyuYbOCdRHgfDRZaHOWqS-sQ4PU2aFsp_iJ1gOjWMjFBpzcyLk_hUZe5OY5MIOcKDGq7RlUCFUaKjSK09SN8XccKXCb4NSHG2lb-pw6cEwiMoEQGVGFjMgiowkfV_DTqujHtZDvEFf_BdqsURlZDlFGf-m5CW9Xn_Fuk8NG5aaYIwyuHQ3Ylu814VlFAqupBOkcbY57-3SFJqIqf_aapbz491LewJ3uce8wOtzvH7yEu5zeFpbBnZvQmJ3PzStUwGbxa0vlDE5v-mL9AXkIRFI
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=Serum+Angiopoietin-like+Protein+6%2C+Risk+of+Type+2+Diabetes%2C+and+Response+to+Hyperglycemia%3A+A+Prospective+Cohort+Study&rft.jtitle=The+journal+of+clinical+endocrinology+and+metabolism&rft.au=Fan%2C+Kang-Chih&rft.au=Wu%2C+Hung-Tsung&rft.au=Wei%2C+Jung-Nan&rft.au=Chuang%2C+Lee-Ming&rft.date=2020-05-01&rft.pub=Copyright+Oxford+University+Press&rft.issn=0021-972X&rft_id=info:doi/10.1210%2Fclinem%2Fdgaa103&rft.externalDocID=10.1210%2Fclinem%2Fdgaa103
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0021-972X&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0021-972X&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0021-972X&client=summon