Evidence map›Paper›PMID 39498871›Full record

ArticleGenetic epidemiology2025

A Novel One-Sample Mendelian Randomization Approach for Count-Type Outcomes That Is Robust to Correlated and Uncorrelated Pleiotropic Effects.

Janaka S S Liyanage, Jane S Hankins, Jeremie H Estepp, Deokumar Srivastava, Sara R Rashkin, Clifford Takemoto, Yun Li, Yuehua Cui, Motomi Mori, Mitchell J Weiss and 1 more

Abstract read
In one paragraph

Article in Genetic epidemiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Janaka S S LiyanageBiostatistics Core, Department of Oncology, Karmanos Cancer Institute, School of Medicine, Wayne State University, Detroit, Michigan, USA.ORCID http://orcid.org/0000-0001-9882-0362
Jane S HankinsDepartment of Hematology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Jeremie H EsteppDepartment of Hematology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Deokumar SrivastavaDepartment of Biostatistics, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Sara R RashkinDepartment of Hematology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.ORCID http://orcid.org/0000-0001-5542-6891
Clifford TakemotoDepartment of Hematology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Yun LiDepartment of Biostatistics, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Yuehua CuiDepartment of Statistics and Probability, Michigan State University, East Lansing, Michigan, USA.
Motomi MoriDepartment of Biostatistics, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Mitchell J WeissDepartment of Hematology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Guolian KangDepartment of Biostatistics, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
Tumor Biology and Microenvironment (Program 1)P30CA022453 · NCI · WAYNE STATE UNIVERSITY · PI Julie Lynn Boerner · 1985 to 2026
$68.4M
NCI NIH HHS P30 CA021765NCI NIH HHS P30 CA022453This research was supported by the American Lebanese Syrian Associated Charities (ALSAC), NIH Center grant P30 CA021765 to the St. Jude Comprehensive Cancer Center at St. Jude Children's Research Hospital, and P30 CA022453 to the Karmanos Cancer Institute at Wayne State University.
6 · The paper itself

Abstract

We propose two novel one-sample Mendelian randomization (MR) approaches to causal inference from count-type health outcomes, tailored to both equidispersion and overdispersion conditions. Selecting valid single-nucleotide polymorphisms (SNPs) as instrumental variables (IVs) poses a key challenge for MR approaches, as it requires meeting the necessary IV assumptions. To bolster the proposed approaches by addressing violations of IV assumptions, we incorporate a process for removing invalid SNPs that violate the assumptions. In simulations, our proposed approaches demonstrate robustness to the violations, delivering valid estimates, and interpretable type-I errors and statistical power. This increases the practical applicability of the models. We applied the proposed approaches to evaluate the causal effect of fetal hemoglobin (HbF) on the vaso-occlusive crisis and acute chest syndrome (ACS) events in patients with sickle cell disease (SCD) and revealed the causal relation between HbF and ACS events in these patients. We also developed a user-friendly Shiny web application to facilitate researchers' exploration of causal relations.

Indexed as

Anemia, Sickle CellGenetic PleiotropyMendelian Randomization AnalysisPolymorphism, Single NucleotideCausalityComputer SimulationFetal HemoglobinHumansModels, GeneticModels, StatisticalFetal Hemoglobincount datageneralized linear modelsgenetic causal inferencesinstrumental variablesMendelian randomization

Identifiers

PMID39498871
PMCPMC12107484

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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.