Evidence map›Paper›PMID 38828596›Full record

ArticleCirculation research2024

Imbalance of APOB Lipoproteins and Large HDL in Type 1 Diabetes Drives Atherosclerosis.

Vishal Kothari, Tse W W Ho, Ainara G Cabodevilla, Yi He, Farah Kramer, Masami Shimizu-Albergine, Jenny E Kanter, Janet Snell-Bergeon, Edward A Fisher, Baohai Shao and 6 more

Abstract read
In one paragraph

Article in Circulation research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Vishal KothariDepartment of Medicine, Division of Metabolism, Endocrinology and Nutrition, UW Medicine Diabetes Institute (V.K., Y.H., F.K., M.S.-A., J.E.K., B.S., J.W.H., T.V., K.E.B.).ORCID 0000-0002-3612-8810
Tse W W HoKeenan Centre for Biomedical Research, St. Michael's Hospital, Toronto, Canada (T.W.W.H., W.L.L.).ORCID 0000-0003-4465-7859
Ainara G CabodevillaDivision of Endocrinology, Diabetes and Metabolism (A.G.C., I.J.G.).ORCID 0000-0002-4026-7637
Yi HeDepartment of Medicine, Division of Metabolism, Endocrinology and Nutrition, UW Medicine Diabetes Institute (V.K., Y.H., F.K., M.S.-A., J.E.K., B.S., J.W.H., T.V., K.E.B.).
Farah KramerDepartment of Medicine, Division of Metabolism, Endocrinology and Nutrition, UW Medicine Diabetes Institute (V.K., Y.H., F.K., M.S.-A., J.E.K., B.S., J.W.H., T.V., K.E.B.).
Masami Shimizu-AlbergineDepartment of Medicine, Division of Metabolism, Endocrinology and Nutrition, UW Medicine Diabetes Institute (V.K., Y.H., F.K., M.S.-A., J.E.K., B.S., J.W.H., T.V., K.E.B.).ORCID 0000-0002-7989-6051
Jenny E KanterDepartment of Medicine, Division of Metabolism, Endocrinology and Nutrition, UW Medicine Diabetes Institute (V.K., Y.H., F.K., M.S.-A., J.E.K., B.S., J.W.H., T.V., K.E.B.).ORCID 0000-0003-3212-772X
Janet Snell-BergeonBarbara Davis Center for Diabetes, University of Colorado Denver, Aurora (J.S.-B.).ORCID 0000-0002-9337-3740
Edward A FisherDivision of Cardiology, Department of Medicine, New York University Grossman School of Medicine (E.A.F.).
Baohai ShaoDepartment of Medicine, Division of Metabolism, Endocrinology and Nutrition, UW Medicine Diabetes Institute (V.K., Y.H., F.K., M.S.-A., J.E.K., B.S., J.W.H., T.V., K.E.B.).ORCID 0000-0001-8832-2845
Jay W HeineckeDepartment of Medicine, Division of Metabolism, Endocrinology and Nutrition, UW Medicine Diabetes Institute (V.K., Y.H., F.K., M.S.-A., J.E.K., B.S., J.W.H., T.V., K.E.B.).
Jacob O WobbrockThe Information School (J.O.W.).ORCID 0000-0003-3675-5491
Warren L LeeKeenan Centre for Biomedical Research, St. Michael's Hospital, Toronto, Canada (T.W.W.H., W.L.L.).ORCID 0000-0002-1788-6587
Ira J GoldbergDivision of Endocrinology, Diabetes and Metabolism (A.G.C., I.J.G.).ORCID 0000-0002-8701-2201
Tomas VaisarDepartment of Medicine, Division of Metabolism, Endocrinology and Nutrition, UW Medicine Diabetes Institute (V.K., Y.H., F.K., M.S.-A., J.E.K., B.S., J.W.H., T.V., K.E.B.).ORCID 0000-0002-7406-6606
Karin E BornfeldtDepartment of Medicine, Division of Metabolism, Endocrinology and Nutrition, UW Medicine Diabetes Institute (V.K., Y.H., F.K., M.S.-A., J.E.K., B.S., J.W.H., T.V., K.E.B.).ORCID 0000-0001-9208-6523

Funding

Vector and Transgenic Mouse CoreP30DK017047 · NIDDK · UNIVERSITY OF WASHINGTON · PI Sakeneh Zraika · 1986 to 2026
$41.4M
Resolving Macrophage Inflammation in Atherosclerotic Plaques and Other Sites in Insulin ResistanceP01HL131481 · NHLBI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ANN MARIE SCHMIDT · 2017 to 2026
$27.3M
Project 3 - HDL Structure/Function in LCAT Deficient HumansP01HL128203 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Jere P Segrest · 2016 to 2026
$25.1M
Triglycerides, Diabetes and Cardiovascular DiseaseP01HL151328 · NHLBI · UNIVERSITY OF WASHINGTON · PI Karin E Bornfeldt · 2020 to 2026
$19.6M
Identifying new strategies for prevention of cardiovascular complications of diabetesR35HL150754 · NHLBI · UNIVERSITY OF WASHINGTON · PI BORNFELDT, KARIN E · 2020 to 2025
$6.2M
Apolipoprotein C3-loading of apolipoprotein B100 lipoproteins and cardiovascular disease in patients with type 1 diabetesR01HL161829 · NHLBI · UNIVERSITY OF WASHINGTON · PI HEINECKE, JAY W · 2022 to 2025
$3.3M
Chylomicrons and endothelial biologyR01HL160891 · NHLBI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Ira J Goldberg · 2023 to 2026
$3.3M
Structural basis for cardioprotective HDLR01HL149685 · NHLBI · UNIVERSITY OF WASHINGTON · PI BORNFELDT, KARIN E., HEINECKE, JAY W · 2020 to 2023
$2.8M
NHLBI NIH HHS P01 HL128203NHLBI NIH HHS P01 HL131481NHLBI NIH HHS P01 HL151328NHLBI NIH HHS R01 HL149685NHLBI NIH HHS R01 HL160891NHLBI NIH HHS R01 HL161829NHLBI NIH HHS R35 HL150754NIDDK NIH HHS P30 DK017047
6 · The paper itself

Abstract

backgroundIndividuals with type 1 diabetes (T1D) generally have normal or even higher HDL (high-density lipoprotein)-cholesterol levels than people without diabetes yet are at increased risk for atherosclerotic cardiovascular disease (CVD). Human HDL is a complex mixture of particles that can vary in cholesterol content by >2-fold. To investigate if specific HDL subspecies contribute to the increased atherosclerosis associated with T1D, we created mouse models of T1D that exhibit human-like HDL subspecies. We also measured HDL subspecies and their association with incident CVD in a cohort of people with T1D.

methodsWe generated LDL receptor-deficient (

resultsDiabetic

conclusionsOur results suggest that the balance between APOB lipoproteins and the larger HDL subspecies contributes to atherosclerosis progression and incident CVD in the setting of T1D and that larger HDLs exert atheroprotective effects on endothelial cells rather than by promoting macrophage cholesterol efflux.

Indexed as

Apolipoprotein A-IAtherosclerosisDiabetes Mellitus, Type 1Receptors, LDLAdultAnimalsApolipoprotein B-100Cholesterol Ester Transfer ProteinsDisease Models, AnimalFemaleHumansLipoproteins, HDLMaleMiceMice, Inbred C57BLMice, KnockoutAPOA1 protein, humanAPOB protein, humanApob protein, mouseApolipoprotein A-IApolipoprotein B-100CETP protein, humanCholesterol Ester Transfer ProteinsLipoproteins, HDLReceptors, LDLatherosclerosiscardiovascular diseasescholesteroldiabetes mellituslipoproteins, HDLtranscytosis

Identifiers

PMID38828596
PMCPMC11223987

What Socratic holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.