Evidence map›Paper›PMID 42491262›Full record

ArticleSubstance use : research and treatment

Comparing Regression Adjustment, Matching, and Inverse Probability Weights in Small Sub-Populations in the HIV SUCCESS Consortium: A Real-World Data Example.

Lydia N Drumright, Ryan P Kyle, Dominique Heinke, Sonia Napravnik, Geetanjali Chander, Catherine R Lesko, Ross A Baiers, Brian Mustanski, Edward Cachay, Michele Kipke and 14 more

Abstract read
In one paragraph

Article in Substance use : research and treatment. 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

24 authors.

Lydia N DrumrightUniversity of Washington, Seattle, WA, USA.ORCID https://orcid.org/0000-0002-3361-8080
Ryan P KyleUniversity of Washington, Seattle, WA, USA.
Dominique HeinkeUniversity of Washington, Seattle, WA, USA.
Sonia NapravnikUniversity of North Carolina, Chapel Hill, NC, USA.
Geetanjali ChanderUniversity of Washington, Seattle, WA, USA.
Catherine R LeskoJohns Hopkins University, Baltimore, MD, USA.
Ross A BaiersNorthwestern University, Evanston, IL, USA.
Brian MustanskiNorthwestern University, Evanston, IL, USA.
Edward CachayMayo Clinic School of Medicine, Phoenix, AZ, USA.
Michele KipkeUniversity of Sothern California, Los Angeles, CA, USA.
Richard D MooreJohns Hopkins University, Baltimore, MD, USA.
Kenneth H MayerFenway Institute, Boston, MA, USA.
Luis ParraUniversity of Michigan, Ann Arbor, MI, USA.
Rob J FredericksenUniversity of Washington, Seattle, WA, USA.
Sari ReisnerFenway Institute, Boston, MA, USA.
Katerina ChristopoulosUniversity of California, San Francisco, CA, USA.
George A YendewaCase Western Reserve University, Cleveland, OH, USA.
Marianna BaumFlorida International University, Miami, FL, USA.
Laura BamfordNorthwestern University, Evanston, IL, USA.
Mari M KitahataUniversity of Washington, Seattle, WA, USA.
Michael S SaagUniversity of Alabama, Birmingham, AL, USA.
Heidi M CraneUniversity of Washington, Seattle, WA, USA.
Joseph A C DelaneyUniversity of Washington, Seattle, WA, USA.ORCID https://orcid.org/0000-0003-1771-1776
Bridget M WhitneyUniversity of Washington, Seattle, WA, USA.

Funding

University of Washington/Fred Hutch Center for AIDS ResearchP30AI027757 · NIAID · UNIVERSITY OF WASHINGTON · PI CONNIE L CELUM · 1988 to 2026
$104.9M
Unsolicited R24 for the CFAR-Network of Integrated Clinical Sciences, CNICSR24AI067039 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Michael S. Saag · 2006 to 2026
$99.4M
Virology CoreP30AI027767 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Paul A. Goepfert · 1988 to 2026
$84.1M
Virology, Immunology, and Microbiology CoreP30AI050410 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DAVID M. MARGOLIS · 2001 to 2026
$76.9M
The RADAR cohort study of multilevel Influences on HIV and substance useU01DA036939 · NIDA · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Brian Mustanski, Michael E Newcomb · 2014 to 2026
$29.5M
Johns Hopkins HIV Clinical CohortU01DA036935 · NIDA · JOHNS HOPKINS UNIVERSITY · PI MOORE, RICHARD DOUGLAS · 2014 to 2024
$14.9M
3/4 Alcohol Research Consortium in HIV - Epidemiological Research Arm (ARCH-ERA)U01AA020793 · NIAAA · UNIVERSITY OF WASHINGTON · PI CRANE, HEIDI M., LAU, BRYAN · 2011 to 2020
$5.8M
Integration of Evidence-based Alcohol Interventions into HIV CareU01AA020802 · NIAAA · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI CROPSEY, KAREN L, MUGAVERO, MICHAEL J · 2011 to 2020
$4.2M
HIV and Substance Use Cohort Coordinating Center for Emerging and High Impact Scientific Cross Cohort Studies: HIV SUCCESSU24DA058307 · NIDA · UNIVERSITY OF WASHINGTON · PI GEETANJALI CHANDER, Heidi M. Crane · 2023 to 2026
$3.6M
1/4 Alcohol Research Consortium in HIV-Administrative Core (ARCH-AC)U24AA020801 · NIAAA · JOHNS HOPKINS UNIVERSITY · PI CHANDER, GEETANJALI, MCCAUL, MARY E · 2011 to 2021
$3.5M
NIAAA NIH HHS U01 AA020793NIAAA NIH HHS U01 AA020802NIAAA NIH HHS U24 AA020801NIAID NIH HHS P30 AI027757NIAID NIH HHS P30 AI027767NIAID NIH HHS P30 AI050410NIAID NIH HHS R24 AI067039NIDA NIH HHS U01 DA036935NIDA NIH HHS U01 DA036939NIDA NIH HHS U24 DA058307
6 · The paper itself

Abstract

Objectives: To understand the trade-offs between different statistical modeling approaches, using real world data with small sub-populations, with rare exposures and increasingly rare outcomes. In particular, to compare adjusted regression, inverse probability weighting, and matching. Methods: Data for these analyses came from the RADAR (N=1,134) and combined CNICS/JHHCC (N=14,434) cohorts. We estimated prevalence ratios (PRs) for self-reported use of specific substances comparing subpopulations (SP), SP-1 vs SP-3 and SP-2 vs SP-3, where SP-1 was the largest proportion (92% in RADAR, 81% in CNICS/JHHCC), SP2 was moderate proportion (18% in CNICS/JHHCC) and SP-3 was the smallest proportion (8% in RADAR, 1% in CNICS/JHHCC) of the population. We calculated PRs using 1) unadjusted relative risk regression (RR); and adjusted estimates controlling for age, race/ethnicity, study site, and year of interview using: 2) standard adjustment in RR; 3) stabilized inverse probability of treatment weighting (IPTW); and 4) matching with up to 3 matches from SP-1 or SP-2 per SP-3 participant. Results: For most substances, all methods yielded consistent estimates. There were large weights in some of the IPTW analyses and in three cases these resulted in substantially divergent estimates. For the comparison between SP-1 and SP-3, the estimate for smoking was 1.3-fold greater in the matched analysis (PR=1.33, 95% CI: 1.02-1.75) than in IPTW (PR=1.03, 95% CI: 0.78-1.37 ATE and PR=1.05, 95% CI: 0.88-1.26 ATT). Even more extreme divergence in estimates was observed for differences between SP-2 and SP-3 with respect to methamphetamine/amphetamine, (IPTW-ATE: PR=1.51, 95% CI: 0.79-2.89; IPTW-ATT: PR=2.36, 95% CI: 1.36-4.12); vs Matching: PR=2.71, 95%CI: 1.47-4.99) and cocaine (IPTW-ATE: PR=1.15, 95% CI: 0.55-2.38; IPTW-ATT: PR=1.81, 95% CI: 1.03-3.18); vs Matching: PR=1.38, 95%CI: 0.76-2.53). Conclusion: The combination of a rare exposure and a rare outcome can produce challenges for commonly used confounding adjustment strategies, and it is often best to compare different modeling approaches to gain greater insight.

Indexed as

inverse probability of treatment weighting (IPTW)matchingpositivitysmall populationsmall samplessparse data bias

Identifiers

PMID42491262
PMCPMC13376484

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.