Evidence map›Paper›PMID 34690220›Full record

ArticleJournal of atherosclerosis and thrombosis2022

Prospective Registry Study of Primary Dyslipidemia (PROLIPID): Rationale and Study Design.

Hayato Tada, Tomoyuki Kurashina, Masatsune Ogura, Misa Takegami, Yoshihiro Miyamoto, Hidenori Arai, Mariko Harada-Shiba, Shun Ishibashi

Open access · diamondAbstract readMulticenter Study
In one paragraph

Article in Journal of atherosclerosis and thrombosis, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.3field-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

7 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Transitional Medicine of Intractable Primary Dyslipidemias in Japan.Journal of atherosclerosis and thrombosis · 2024
    Review
  3. A fascinating association between HDL as a multi-potent particle and hypertension.Hypertension research : official journal of the Japanese Society of Hypertension · 2024
    Article
  4. Article
  5. Article
  6. Article
  7. 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

8 authors at 5 institutions in 1 country.

Hayato TadaDepartment of Cardiovascular Medicine, Kanazawa University Graduate School of Medical Sciences.
Tomoyuki KurashinaDivision of Endocrinology and Metabolism, Department of Internal Medicine, School of Medicine, Jichi Medical University.
Masatsune OguraDepartment of General Medical Science, Chiba University Graduate School of Medicine.
Misa TakegamiDepartment of Preventive Medicine and Epidemiology, National Cerebral and Cardiovascular Center Research Institute.
Yoshihiro MiyamotoDepartment of Preventive Cardiology, National Cerebral and Cardiovascular Center.
Hidenori AraiNational Center for Geriatrics and Gerontology.
Mariko Harada-ShibaDepartment of Molecular Pathogenesis, National Cerebral and Cardiovascular Center Research Institute.
Shun IshibashiDivision of Endocrinology and Metabolism, Department of Internal Medicine, School of Medicine, Jichi Medical University.
National Cerebral and Cardiovascular Center · JPJichi Medical University · JPChiba University · JPKanazawa University · JPNational Center for Geriatrics and Gerontology · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionPrimary dyslipidemias are inherited disorders in plasma lipoprotein metabolism that lead to serious cardiovascular and other complications. The Japanese Ministry of Health, Labor and Welfare (MHLW) covers medical expenses, under the Research Program on Rare and Intractable Diseases, for homozygous familial hypercholesterolemia (FH), familial chylomicronemia, sitosterolemia, cerebrotendinous xanthomatosis, lecithin:cholesterol acyltransferase deficiency, Tangier disease, and abetalipoproteinemia. Apolipoprotein A1 deficiency, heterozygous FH, and type III hyperlipoproteinemia are covered by the MHLW Pediatric Chronic Disease Program. Heterozygous FH and type III hyperlipoproteinemia are also important for their relatively common prevalence and, accordingly, high impact on Japanese public health by significant contribution to the overall prevalence of cardiovascular diseases. Therefore, a systemic survey of these diseases is mandatory to estimate their actual situation, such as prevalence, clinical manifestations, and prognoses among the Japanese population. The impact of these rare and intractable diseases on cardiovascular and other complications will likely be higher among Japanese people than other ethnicities because the general Japanese population has many cardioprotective aspects. The current study intends to conduct a multicenter registry of these diseases to assess their demographics and clinical features comprehensively. METHODS AND ANALYSIS: The Prospective Registry Study of Primary Dyslipidemia is a registry-based prospective, observational, multicenter cohort study in Japan, enrolling patients who fulfill the Japanese clinical criteria of the primary dyslipidemias listed above, from 26 participating institutes from August 2015 to March 2023. A total of 1,000 patients will be enrolled in the study and followed for 10 years. Clinical parameters are collected, including physical and laboratory findings, genetic analysis, drugs, lifestyle management, and clinical events, especially cardiovascular events. The primary endpoint of this study is the new onset of cardiovascular disease and acute pancreatitis, and the secondary endpoint is death from any causes. ETHICS AND DISSEMINATION: This study complies with the Declaration of Helsinki, the Ethical Guidelines for Medical and Health Research Involving Human Subjects, and all other applicable laws and guidelines in Japan. The institutional review boards have approved this study protocol at all participating institutes. The final results are to be published at appropriate international conferences and in peer-reviewed journals.

Indexed as

Cardiovascular DiseasesDyslipidemiasHyperlipoproteinemia Type IIHyperlipoproteinemia Type IIIPancreatitisAcute DiseaseChildCohort StudiesHumansRegistriesDyslipidemiaGeneticsIntractable diseaseRegistry

Identifiers

PMID34690220
PMCPMC9174082
OpenAlexW3208934879

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.