Evidence map›Paper›PMID 1415225›Full record

ArticleAmerican journal of human genetics1992

Lipoprotein(a) in women twins: heritability and relationship to apolipoprotein(a) phenotypes.

M A Austin, C Sandholzer, J V Selby, B Newman, R M Krauss, G Utermann

2 registry-linked trialsAbstract read
In one paragraph

Article in American journal of human genetics, 1992. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
9.9field-weighted citation impact, top 2% 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.

NCT00005203 completednot on this map

Genetics of Low Density Lipoprotein Subclasses in Hypercholesterolemia

TypeobservationalSponsorUniversity of WashingtonRan1987 to 1992ConditionsCardiovascular Diseases, Heart Diseases, Hypercholesterolemia
NCT00005239 completednot on this map

Genetic Epidemiology of Coronary Heart Disease Risk in Women Twins

TypeobservationalSponsorNational Heart, Lung, and Blood Institute (NHLBI)Ran1989 to 1991ConditionsCardiovascular Diseases, Coronary Disease, Heart Diseases
3 · Its place in the literature

Who cites it

29 citing papers in PubMed, 116 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Lipoprotein(a).Handbook of experimental pharmacology · 2022
    Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. Article
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  20. Review
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

6 authors at 1 institution in 1 country.

M A AustinDepartment of Epidemiology, School of Public Health and Community Medicine, University of Washington, Seattle 98195.
C Sandholzer
J V Selby
B Newman
R M Krauss
G Utermann
University of Washington · US

Funding

GENETIC EPIDEMIOLOGY OF CHD RISK FACTORS IN WOMEN TWINSR01HL041830 · NHLBI · KAISER FOUNDATION HOSPITALS · PI SELBY, JOE V · 1989 to 1991
–
NHLBI NIH HHS HL-387B0NHLBI NIH HHS HL-41830PHS HHS R-01
6 · The paper itself

Abstract

Lp(a) is a unique lipoprotein consisting of an LDL-like particle and a characteristic protein, apo(a). Increased levels of Lp(a) constitute a risk factor for coronary heart disease. Variation in the size of the apo(a) protein is a phenotype controlled by the apo(a) gene on chromosome 6 and is related to Lp(a) plasma levels. Based on 169 MZ and 125 DZ adult female twin pairs, this study's purpose was to estimate the proportion of the variation in Lp(a) levels that is due to genetic influences and to determine the extent to which the apo(a) locus explains this heritability. Lp(a) levels were significantly more similar in MZ twins than in DZ twins: mean co-twin differences were 3.9 +/- 5.7 mg/dl and 16.0 +/- 19.9 mg/dl (P less than .001), respectively. Intraclass correlations were .94 in MZ twins and .32 in DZ twins, resulting in a heritability estimate of .94 (P less than .001). Heritability was then calculated using only co-twins with the same apo(a) phenotype: the heritability estimate decreased to .45 but was still highly significant (P less than .001). Therefore, on the basis of heritability analysis of women twins, Lp(a) levels are almost entirely genetically controlled. Variation at the apo(a) locus contributes to this heritability, although other genetic factors could be involved.

Indexed as

AdultAnalysis of VarianceApolipoproteins AEnzyme-Linked Immunosorbent AssayFemaleHumansLipoprotein(a)PhenotypeTwinsTwins, DizygoticTwins, MonozygoticApolipoproteins ALipoprotein(a)

Identifiers

PMID1415225
PMCPMC1682765
OpenAlexW1579995061

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.