Evidence map›Paper›PMID 29077935›Full record

ArticleThe Journal of clinical endocrinology and metabolism2018

Glycation Reduces the Stability of ApoAI and Increases HDL Dysfunction in Diet-Controlled Type 2 Diabetes.

Sangeeta R Kashyap, Abdullah Osme, Serguei Ilchenko, Makan Golizeh, Kwangwon Lee, Shuhui Wang, James Bena, Stephen F Previs, Jonathan D Smith, Takhar Kasumov

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical endocrinology and metabolism, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed, 1 pooled it
5.5field-weighted citation impact, top 3% of its field
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

60 citing papers in PubMed, 1 synthesis or guideline pooled it, 91 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. HDL metabolism and function in diabetes mellitus.Nature reviews. Endocrinology · 2026
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
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  15. Review
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  18. Dysfunctional high-density lipoprotein: an updated review.Frontiers in cardiovascular medicine · 2025
    Review
  19. Article
  20. Article
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

10 authors at 3 institutions in 1 country.

Sangeeta R KashyapDepartment of Endocrinology and Metabolism, Cleveland Clinic, Cleveland, Ohio.
Abdullah OsmeDepartment of Pharmaceutical Sciences, Northeast Ohio Medical University, Rootstown, Ohio.
Serguei IlchenkoDepartment of Pharmaceutical Sciences, Northeast Ohio Medical University, Rootstown, Ohio.
Makan GolizehDepartment of Pharmaceutical Sciences, Northeast Ohio Medical University, Rootstown, Ohio.
Kwangwon LeeDepartment of Pharmaceutical Sciences, Northeast Ohio Medical University, Rootstown, Ohio.
Shuhui WangDepartment of Cellular & Molecular Medicine, Cleveland Clinic, Cleveland, Ohio.
James BenaDepartment of Quantitative Health Sciences, Cleveland Clinic, Cleveland, Ohio.
Stephen F PrevisMerck Research Laboratories, Kenilworth, New Jersey.
Jonathan D SmithDepartment of Cellular & Molecular Medicine, Cleveland Clinic, Cleveland, Ohio.
Takhar KasumovDepartment of Pharmaceutical Sciences, Northeast Ohio Medical University, Rootstown, Ohio.
Northeast Ohio Medical University · USCleveland Clinic · USMerck & Co., Inc., Rahway, NJ, USA (United States) · US

Funding

Novel computational methods for in vivo proteome dynamics estimation using heavy water metabolic labeling and LC-MSR01GM112044 · NIGMS · UNIVERSITY OF TEXAS MED BR GALVESTON · PI SADYGOV, ROVSHAN G · 2015 to 2023
$2.7M
NIGMS NIH HHS R01 GM112044
6 · The paper itself

Abstract

Context: Hyperglycemia plays a key role in the pathogenesis of cardiovascular complications of diabetes. Type 2 diabetes mellitus (T2DM) is associated with high-density lipoprotein (HDL) dysfunction and increased degradation of apolipoprotein I (ApoAI). The mechanism(s) of these changes is largely unknown. Objective: To study the role of hyperglycemia-induced glycation on ApoAI kinetics and stability in patients with diet-controlled T2DM. Design: 2H2O-metabolic labeling approach was used to study ApoAI turnover in patients with diet-controlled T2DM [n = 9 (5 F); 59.3 ± 8.5 years] and matched healthy controls [n = 8 (4 F); 50.7 ± 11.6 years]. The effect of Amadori glycation on in vivo ApoAI stability and the antioxidant and cholesterol efflux properties of HDL were assessed using a proteomics approach and in vitro assays. Results: Patients with T2DM had increased turnover of ApoAI and impaired cholesterol efflux and antioxidant properties of HDL. Glycated hemoglobin was negatively correlated with the half-life of ApoAI and cholesterol efflux function of HDL. Proteomics analysis identified several nonenzymatic early (Amadori) glycations of ApoAI at lysine sites. The kinetics analysis of glycated and native ApoAI peptides in patients with T2DM revealed that glycation resulted in a threefold shorter ApoAI half-life. Conclusions: The 2H2O method allowed the detection of early in vivo impairments in HDL metabolism and function that were related to hyperglycemia-induced glycation of ApoAI in T2DM.

Indexed as

AdultAgedAnimalsApolipoprotein A-ICase-Control StudiesCells, CulturedDiabetes Mellitus, Type 2DietDyslipidemiasFemaleGlycosylationHumansHyperglycemiaLipoproteins, HDLMaleMiceApolipoprotein A-ILipoproteins, HDL

Identifiers

PMID29077935
PMCPMC5800833
OpenAlexW2765711746

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.