Evidence map›Paper›PMID 32685870›Full record

ArticleJournal of the Endocrine Society2020

PCSK9 in African Americans and Caucasians in Relation to Lp(a) Level, Apo(a) Size and Heritability.

Byambaa Enkhmaa, Kyoungmi Kim, Wei Zhang, Nishant Prakash, Kevin Truax, Erdembileg Anuurad, Lars Berglund

Open access · goldAbstract read
In one paragraph

Article in Journal of the Endocrine Society, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 2 pooled it
1.4field-weighted citation impact, top 18% 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

9 citing papers in PubMed, 2 syntheses or guidelines pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Article
  6. Effects of theGenes · 2025
    Article
  7. Article
  8. The evolving landscape of PCSK9 inhibition in cancer.European journal of pharmacology · 2023
    Review
  9. Bridging the Racial Disparity Gap in Lipid-Lowering Therapy.Journal of the American Heart Association · 2021
    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

7 authors at 1 institution in 1 country.

Byambaa EnkhmaaDepartments of Internal Medicine, University of California, Davis, CA, USA.ORCID 0000-0002-1429-6864
Kyoungmi KimPublic Health Sciences, University of California, Davis, CA, USA.
Wei ZhangDepartments of Internal Medicine, University of California, Davis, CA, USA.
Nishant PrakashDepartments of Internal Medicine, University of California, Davis, CA, USA.
Kevin TruaxDepartments of Internal Medicine, University of California, Davis, CA, USA.
Erdembileg AnuuradDepartments of Internal Medicine, University of California, Davis, CA, USA.
Lars BerglundDepartments of Internal Medicine, University of California, Davis, CA, USA.
University of California, Davis · US

Funding

UC Davis Clinical and Translational Science CenterUL1TR001860 · NCATS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI KENYON, NICHOLAS J., LYLES, COURTNEY REES · 2016 to 2025
$47.3M
Building Interdisciplinary Research Careers in Womens Health at UC Davis - Administrative SupplementK12HD051958 · NICHD · UNIVERSITY OF CALIFORNIA DAVIS · PI LANE, NANCY E · 2005 to 2023
$9.6M
Regulation of Lipoprotein(a) Metabolism in Humans with Reference to EthnicityR01HL062705 · NHLBI · UNIVERSITY OF CALIFORNIA DAVIS · PI BERGLUND, LARS F · 2000 to 2011
$2.9M
NCATS NIH HHS UL1 TR001860NHLBI NIH HHS R01 HL062705NICHD NIH HHS K12 HD051958
6 · The paper itself

Abstract

contextInhibition of proprotein convertase subtilisin/kexin type 9 (PCSK9) reduces lipoprotein(a) [Lp(a)] levels, but the association of PCSK9 with Lp(a) level and its major determinant, apolipoprotein(a) [apo(a)] size, is not fully understood.

objectiveTo assess the relationship between PCSK9, Lp(a) level, apo(a) size, age, and ethnicity/race.

designCross-sectional.

settingGeneral population.

participantsHealthy African Americans and Caucasians (n = 267); age range: 6 to 74 years.

interventionsNone.

main outcome measuresPCSK9 levels, apo(a) isoform and

resultsPlasma PCSK9 levels were significantly higher in African Americans vs Caucasians, in females vs males, and in adults vs children. PCSK9 levels were not associated with total plasma Lp(a) levels either in all participants or in ethnicity-specific analyses. However, PCSK9 levels were significantly positively associated with isoform-specific Lp(a) levels carried by the larger apo(a) size in all participants (

conclusionsAmong African Americans, but not Caucasians, PCSK9 levels were associated with isoform-specific Lp(a) levels carried on larger, but not smaller, apo(a) sizes. The findings illustrate a diverging relationship of PCSK9 with isoform-specific Lp(a) levels across ethnicity.

Indexed as

African AmericansatherogenicityCaucasiansethnicityfamilygeneral population

Identifiers

PMID32685870
PMCPMC7358566
OpenAlexW3034894861

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.