Evidence map›Paper›PMID 29185378›Full record

ArticleMedical decision making : an international journal of the Society for Medical Decision Making2018

Matching Microsimulation Risk Factor Correlations to Cross-sectional Data: The Shortest Distance Method.

Sze-Chuan Suen, Jeremy D Goldhaber-Fiebert, Sanjay Basu

Abstract read
In one paragraph

Article in Medical decision making : an international journal of the Society for Medical Decision Making, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

2 citing papers in PubMed.

  1. Article
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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

3 authors.

Sze-Chuan SuenEpstein Department of Industrial and Systems Engineering, Viterbi School of Engineering, University of Southern California, Los Angeles, CA, USA.
Jeremy D Goldhaber-FiebertStanford Health Policy, Centers for Health Policy and Primary Care and Outcomes Research, Stanford University, Stanford, CA, USA.
Sanjay BasuStanford Health Policy, Centers for Health Policy and Primary Care and Outcomes Research, Stanford University, Stanford, CA, USA.

Funding

Trial of strategies to communicate genetic information to different ethnic and racial subpopulationsU54MD010724 · NIMHD · STANFORD UNIVERSITY · PI CULLEN, MARK RICHARD · 2016 to 2021
$16.3M
Cohort filtering models to identify social program effects on health disparitiesDP2MD010478 · NIMHD · STANFORD UNIVERSITY · PI BASU, SANJAY · 2015 to 2015
$2.4M
Cost-effective chronic disease prevention in developing countriesK01AG037593 · NIA · STANFORD UNIVERSITY · PI GOLDHABER-FIEBERT, JEREMY DAVID · 2011 to 2015
$637k
Studying social factors in sodium consumption to reduce hypertension disparitiesK08HL121056 · NHLBI · STANFORD UNIVERSITY · PI BASU, SANJAY · 2014 to 2017
$599k
NHLBI NIH HHS K08 HL121056NIA NIH HHS K01 AG037593NIMHD NIH HHS DP2 MD010478NIMHD NIH HHS U54 MD010724
6 · The paper itself

Abstract

backgroundMicrosimulation models often compute the distribution of a simulated cohort's risk factors and medical outcomes over time using repeated waves of cross-sectional data. We sought to develop a strategy to simulate how risk factor values remain correlated over time within individuals, and compare it to available alternative methods.

methodsWe developed a method using shortest-distance matching for modeling changes in risk factors in individuals over time, which preserves both the cohort distribution of each risk factor as well as the cross-sectional correlation between risk factors observed in repeated cross-sectional data. We compared the performance of the method with rank stability and regression methods, using both synthetic data and data from the Framingham Offspring Heart Study (FOHS) to simulate a cohort's atherosclerotic cardiovascular disease (ASCVD) risk.

resultsThe correlation between risk factors was better preserved using the shortest distance method than with rank stability or regression (root mean squared difference = 0.077 with shortest distance, v. 0.126 with rank stability and 0.146 with regression in FOHS, and 0.052, 0.426 and 0.352, respectively, in the synthetic data). The shortest distance method generated population ASCVD risk estimate distributions indistinguishable from the true distribution in over 99.8% of cases (Kolmogorov-Smirnov, P > 0.05), outperforming some existing regression methods, which produced ASCVD distributions statistically distinguishable from the true one at the 5% level around 15% of the time. LIMITATIONS: None of the methods considered could predict individual longitudinal trends without error. The shortest-distance method was not statistically inferior to rank stability or regression methods for predicting individual risk factor values over time in the FOHS.

conclusionsA shortest distance method may assist in preserving risk factor correlations in microsimulations informed by cross-sectional data.

Indexed as

Models, StatisticalAgedAge FactorsBiomarkersBlood GlucoseBody Mass IndexComputer SimulationCoronary Artery DiseaseCross-Sectional StudiesFemaleHumansLipidsLongitudinal StudiesMaleMiddle AgedRisk FactorsBiomarkersBlood GlucoseLipidsbiomarker estimationmicrosimulationsrepeated cross sections

Identifiers

PMID29185378
PMCPMC5913001

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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.