Evidence map›Paper›PMID 28401801›Full record

ArticleClinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis2018

Thrombophilia in 153 Patients With Premature Cardiovascular Disease ≤Age 45.

Alexander Milgrom, Kevin Lee, Matan Rothschild, Frini Makadia, Greg Duhon, Sarah Min, Ping Wang, Charles J Glueck

Open access · bronzeAbstract read
In one paragraph

Article in Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

5 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
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  5. 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

8 authors at 1 institution in 1 country.

Alexander Milgrom1 Department of Graduate Medical Education and Research, Internal Medicine Residency Program, Jewish Hospital of Cincinnati, Cincinnati, OH, USA.
Kevin Lee1 Department of Graduate Medical Education and Research, Internal Medicine Residency Program, Jewish Hospital of Cincinnati, Cincinnati, OH, USA.
Matan Rothschild1 Department of Graduate Medical Education and Research, Internal Medicine Residency Program, Jewish Hospital of Cincinnati, Cincinnati, OH, USA.ORCID http://orcid.org/0000-0002-1168-9945
Frini Makadia1 Department of Graduate Medical Education and Research, Internal Medicine Residency Program, Jewish Hospital of Cincinnati, Cincinnati, OH, USA.
Greg Duhon1 Department of Graduate Medical Education and Research, Internal Medicine Residency Program, Jewish Hospital of Cincinnati, Cincinnati, OH, USA.
Sarah Min1 Department of Graduate Medical Education and Research, Internal Medicine Residency Program, Jewish Hospital of Cincinnati, Cincinnati, OH, USA.
Ping Wang1 Department of Graduate Medical Education and Research, Internal Medicine Residency Program, Jewish Hospital of Cincinnati, Cincinnati, OH, USA.
Charles J Glueck1 Department of Graduate Medical Education and Research, Internal Medicine Residency Program, Jewish Hospital of Cincinnati, Cincinnati, OH, USA.
Jewish Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We assessed contributions of thrombophilia to premature cardiovascular disease (CVD) events (≤ age 45) in 153 patients. Test results of thrombophilia-hypofibrinolysis were obtained in 153 patients with CVD ≤ age 45, 110 healthy normal controls, and 110 patients who had venous thromboembolism (VTE) without CVD. Of the 153 patients with CVD, 121 (79%) had sustained myocardial infarction, 70 (46%) had coronary artery stenting, and 53 (35%) had coronary artery bypass grafts. The first CVD events occurred at ages >20 to 35 in 47 patients and at ages >35 to 45 in 106 patients. At study entry, median low-density lipoprotein cholesterol was 126 mg/dL, 56 (37%) smoked, 56 (37%) had hypertension, and 56 (37%) were diabetic. Cases differed from normal controls for high factor VIII (10 [22%] of 45 vs 7 of 103 [7%], P = .007), high homocysteine (32 [21%] of 151 vs 5 [5%] of 107, P = .0002), low free protein S (5 [11%] of 44 vs 2 [2%] of 96, P = .032), high anticardiolipin antibodies (ACLA) IgM (11 [9%] of 129 vs 2 [2%] of 109, P = .024), high lipoprotein (a) [Lp(a)] (46 [30%] of 151 vs 21 [19%] of 110, P = .038), and the lupus anticoagulant (4 [11%] of 37 vs 2 [2%] of 110, P = .035). There were no differences ( P > .05) between cases and VTE controls except free protein S and Lp(a). Free protein S was more often low in VTE controls (24 [28%] of 85 vs 5 [11%] of 44, P = .03) and Lp(a) was more often high in cases (46 [30%] of 151, VTE controls 12 [17%] of 71, P = .032). In 153 patients with premature CVD ≤ age 45, thrombophilia was pervasive (high factor VIII, homocysteine, ACLA IgM, low free protein S, high Lp(a), and lupus anticoagulant), evidencing thrombotic contribution to premature CVD. Moreover, thrombophilia in patients with premature CVD was comparable to VTE controls, emphasizing the pervasive nature of thrombophilia in premature CVD.

Indexed as

AdolescentAdultAge FactorsBiomarkersCardiovascular DiseasesCase-Control StudiesFemaleHumansMaleMiddle AgedRisk FactorsThrombophiliaVenous ThromboembolismYoung AdultBiomarkersatherosclerosisclinical thrombophiliathrombophiliavascular diseasevenous thromboembolism

Identifiers

PMID28401801
PMCPMC6714667
OpenAlexW2607415432

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.