Evidence map›Paper›PMID 24973831›Full record

ArticleIndian heart journal

Relook at lipoprotein (A): independent risk factor of coronary artery disease in north Indian population.

Jamal Yusuf, Neeraj Yadav, Saibal Mukhopadhyay, Abhishek Goyal, Vimal Mehta, Vijay Trehan, Sanjay Tyagi

Abstract read
In one paragraph

Article in Indian heart journal. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

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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.

  1. Review
  2. Lipoprotein(a) and premature myocardial infarction: Mechanistic insights and implications for PCI-era residual risk.International journal of cardiology. Cardiovascular risk and prevention · 2026
    Review
  3. Review
  4. Observational
  5. Article
  6. Vascular Disease in Young Indians (20-40 years): Role of Ischemic Heart Disease.Journal of clinical and diagnostic research : JCDR · 2016
    Review
  7. Article
  8. Review
  9. Observational
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.

Jamal YusufProfessor, Department of Cardiology, G.B. Pant Hospital, New Delhi, India.
Neeraj YadavConsultant Cardiologist, Sterling Hospital, Ahmedabad, India.
Saibal MukhopadhyayProfessor, Department of Cardiology, G.B. Pant Hospital, New Delhi, India.
Abhishek GoyalAssistant Professor, Dayanand Medical College, Ludhiana, India. Electronic address: drabhishekgoyal11@yahoo.in.
Vimal MehtaProfessor, Department of Cardiology, G.B. Pant Hospital, New Delhi, India.
Vijay TrehanProfessor, Department of Cardiology, G.B. Pant Hospital, New Delhi, India.
Sanjay TyagiProfessor & Head, Department of Cardiology, G.B. Pant Hospital, New Delhi, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsLipoprotein (a) [Lp(a)] levels have shown wide ethnic variations. Sparse data on mean Lp(a) levels, its link with clinical variables and severity of coronary artery disease (CAD) in North Indian population needed further studies.

methods150 patients, each of single vessel disease (SVD), double vessel disease (DVD) and triple vessel disease (TVD) with 150 healthy controls were drawn for the study. Serum Lp(a) estimation was performed by immunoturbidimetric method.

resultsLp(a) had a skewed distribution. Median Lp(a) level was significantly raised in cases as compared to controls (median 30.30 vs. 20 mg/dl, p < 0.001). Cases with acute coronary syndrome (ACS, 55.8%) had significantly higher median Lp(a) levels as compared to those with chronic stable angina (35.4 mg/dl vs. 23 mg/dl, p < 0.001). Significant difference in median Lp(a) levels were observed in patients with DVD or TVD versus control (30, 39.05 vs 20 mg/dl, p < 0.008). Lp(a) level was found to be an independent risk factor for CAD (AOR{adjusted odds ratio} 1.018, 95% CI 1.010-1.027; p < 0.001). Analysis using Lp(a) as categorical variable showed that progressive increase in Lp(a) concentration was associated with increased risk of CAD [AOR from lowest to highest quartile (1, 1.04, 1.43 and 2.65, p value for trend = 0.00026)]. Multivariably AOR of CAD for subjects with Lp(a) in the highest quartile (above 40 mg/dl) compared to those with Lp(a) ≤40 mg/dl was 2.308 (95% CI 1.465-3.636, p < 0.001).

conclusionLp(a) above 40 mg/dl (corresponding to 75th percentile)assessed by an isoform insensitive assay is an independent risk factor for CAD. Raised Lp(a) level is also associated with increased risk of ACS and multivessel CAD.

Indexed as

BiomarkersCoronary Artery DiseaseHumansIndiaLipoprotein(a)Risk AssessmentRisk FactorsBiomarkersLipoprotein(a)Coronary artery diseaseLp(a) Lipoprotein(a)North Indian populationRisk factors

Identifiers

PMID24973831
PMCPMC4121757

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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.