Evidence map›Paper›PMID 38486638›Full record

ArticleBiostatistics & epidemiology2023

Analysis of Familial Aggregation Using Recurrence Risk for Complex Survey Data.

Cong Wang, Zhaohai Li, Barry I Graubard

Abstract read
In one paragraph

Article in Biostatistics & epidemiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

3 authors.

Cong WangCenter for Biologics Evaluation and Research, US Food and Drug Administration, Maryland, USA.
Zhaohai LiDepartment of Statistics, The George Washington University, District of Columbia, USA.
Barry I GraubardBiostatistics Branch, National Cancer Institute, Maryland, USA.

Funding

Consultation and CollaborationZIACP010184 · NCI · DIVISION OF CANCER EPIDEMIOLOGY AND GENETICS · PI GRAUBARD, BARRY · 2010 to 2020
$16.3M
Intramural NIH HHS ZIA CP010184
6 · The paper itself

Abstract

Familial or family aggregation of a disease is important for studying possible genetic etiology of a disease. A popular and useful measure of family aggregation is recurrence risk. Household health surveys with (family) network sampling, which surveyed individuals report about disease status of themselves and specified relatives, has been shown to be useful for estimating prevalence of diseases and more recently for estimating recurrence risk of disease using nonparametric classical survey methods. Because these surveys have complex sample designs with sample weighting for differential sample selection rates, this paper extends the composite-likelihood estimation and hypothesis of parameters of the quadratic exponential model (QEM) for simple random samples to data from these complex sample designs. In addition, the QEM is extended to simultaneously estimate and test parameters and recurrence risk for multiple family relationships, for comparing recurrence risk across family-level covariates (e.g., race) and utilizing propensity score weighting to adjust for confounding by individual-level covariates (e.g., age). Simulations are used to study the finite sample properties of the parameter estimation, variance estimation and level and power of hypothesis testing based on derived Wald and Quasi-Score tests for these extended QEMs. Finally, our methods are illustrated using the 1976 National Health Interview Survey diabetes data set.

Indexed as

diabetesextended quadratic exponential modelsnetwork samplingRecurrence risk

Identifiers

PMID38486638
PMCPMC10939038

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Registered trials

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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.