Evidence map›Paper›PMID 39189460›Full record

ArticleJournal of proteome research2024

Missing Values in Longitudinal Proteome Dynamics Studies: Making a Case for Data Multiple Imputation.

Yu Yan, Baradwaj Simha Sankar, Bilal Mirza, Dominic C M Ng, Alexander R Pelletier, Sarah D Huang, Wei Wang, Karol Watson, Ding Wang, Peipei Ping

Abstract read
In one paragraph

Article in Journal of proteome research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

10 authors.

Yu YanDepartments of Physiology and Medicine, University of California, Los Angeles (UCLA) School of Medicine, Los Angeles, California 90095, United States.ORCID 0000-0002-1222-1033
Baradwaj Simha SankarDepartments of Physiology and Medicine, University of California, Los Angeles (UCLA) School of Medicine, Los Angeles, California 90095, United States.
Bilal MirzaDepartments of Physiology and Medicine, University of California, Los Angeles (UCLA) School of Medicine, Los Angeles, California 90095, United States.
Dominic C M NgDepartments of Physiology and Medicine, University of California, Los Angeles (UCLA) School of Medicine, Los Angeles, California 90095, United States.
Alexander R PelletierNHLBI Integrated Cardiovascular Data Science Training Program, UCLA, Los Angeles, California 90095, United States.
Sarah D HuangDepartments of Physiology and Medicine, University of California, Los Angeles (UCLA) School of Medicine, Los Angeles, California 90095, United States.ORCID 0009-0001-6458-4282
Wei WangNHLBI Integrated Cardiovascular Data Science Training Program, UCLA, Los Angeles, California 90095, United States.
Karol WatsonDepartments of Physiology and Medicine, University of California, Los Angeles (UCLA) School of Medicine, Los Angeles, California 90095, United States.
Ding WangDepartments of Physiology and Medicine, University of California, Los Angeles (UCLA) School of Medicine, Los Angeles, California 90095, United States.
Peipei PingDepartments of Physiology and Medicine, University of California, Los Angeles (UCLA) School of Medicine, Los Angeles, California 90095, United States.

Funding

Omics Phenotyping for Identifying Molecular Signatures of the Healthy and Failing Heart: An Integrated Data Science PlatformR35HL135772 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI PING, PEIPEI · 2017 to 2023
$6.4M
Extraction of molecular signature of HFpEF via a machine learning-empowered proteomic characterization: A study of the BCAA pathwayR01HL146739 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI NG, CHUN MING DOMINIC, WANG, DING · 2019 to 2022
$2.6M
NHLBI NIH HHS R01 HL146739NHLBI NIH HHS R35 HL135772
6 · The paper itself

Abstract

Temporal proteomics data sets are often confounded by the challenges of missing values. These missing data points, in a time-series context, can lead to fluctuations in measurements or the omission of critical events, thus hindering the ability to fully comprehend the underlying biomedical processes. We introduce a Data Multiple Imputation (DMI) pipeline designed to address this challenge in temporal data set turnover rate quantifications, enabling robust downstream analysis to gain novel discoveries. To demonstrate its utility and generalizability, we applied this pipeline to two use cases: a murine cardiac temporal proteomics data set and a human plasma temporal proteomics data set, both aimed at examining protein turnover rates. This DMI pipeline significantly enhanced the detection of protein turnover rate in both data sets, and furthermore, the imputed data sets captured new representation of proteins, leading to an augmented view of biological pathways, protein complex dynamics, as well as biomarker-disease associations. Importantly, DMI exhibited superior performance in benchmark data sets compared to single imputation methods (DSI). In summary, we have demonstrated that this DMI pipeline is effective at overcoming challenges introduced by missing values in temporal proteome dynamics studies.

Indexed as

ProteomeProteomicsAnimalsData Interpretation, StatisticalHumansLongitudinal StudiesMiceProteomedata imputationlongitudinal datamultiple imputationprotein turnover rate

Identifiers

PMID39189460
PMCPMC11385379

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.