Evidence map›Paper›PMID 41983645›Full record

ArticleArthritis care & research2026

Real-World Longitudinal Data on the Impact of Hydroxychloroquine Blood Level Monitoring on Lupus Outcomes: Results of a Prospective Longitudinal Cohort Study.

Jay J Patel, Fauzia Hollangel, Caroline Packee, Amita Kapoor, Brad Rovin, Nathalie Costedoat-Chalumeau, Shivani Garg

Abstract read
In one paragraph

Article in Arthritis care & research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

7 authors.

Jay J PatelUniversity of Wisconsin School of Medicine and Public Health, Madison.
Fauzia HollangelUniversity of Wisconsin School of Medicine and Public Health, Madison.
Caroline PackeeUniversity of Wisconsin School of Medicine and Public Health, Madison.
Amita KapoorWisconsin National Primate Research Center, University of Wisconsin-Madison.
Brad RovinOhio State University, Wexner Medical Center, Columbus.ORCID https://orcid.org/0000-0001-5639-0210
Nathalie Costedoat-ChalumeauNational Referral Centre for Rare Autoimmune and Systemic Diseases, Hôpital Cochin, AP-HP Centre and Université Paris Cité and Centre de Recherche en Epidémiologie et Statistiques (CRESS), Unité Inserm 1153, Université de Paris Cité, Paris, France.
Shivani GargUniversity of Wisconsin School of Medicine and Public Health, Madison.ORCID https://orcid.org/0000-0001-7272-2692

Funding

WNPRC Supplemental Request for Nonhuman Primate Enclosures to Equip HIV/AIDS-Related Research FacilitiesP51OD011106 · OD · UNIVERSITY OF WISCONSIN-MADISON · PI Dorota A. Grejner-Brzezinska · 2012 to 2026
$150.7M
Early and Personalized Cardiovascular Disease Preventive Care in Lupus Nephritis (EPiC-LN)K23AR084608 · NIAMS · YALE UNIVERSITY · PI SHIVANI GARG · 2024 to 2026
$512k
Lupus Foundation of AmericaNIAMS NIH HHS 5K23AR084608-02NIAMS NIH HHS K23 AR084608NIAMS NIH HHS P51OD011106NIH HHS P51 OD011106Rheumatology Research Foundation
6 · The paper itself

Abstract

objectiveHydroxychloroquine (HCQ) is a cornerstone therapy in systemic lupus erythematosus (SLE), but the weight-based dosing does not account for clinical factors that can introduce individual variability in drug metabolism and clearance. We leveraged longitudinal data from a prospective SLE cohort to identify clinical factors that predict significant variations in HCQ blood levels despite weight-based HCQ dosing, and we examined if maintaining therapeutic HCQ levels (750-1,150 ng/mL) improved SLE outcomes.

methodsWe analyzed 962 visits from 247 patients in a prospective SLE cohort. Generalized linear mixed models with random intercepts and slopes assessed associations among variables such as chronic kidney disease, HCQ dose, and HCQ blood levels over time. Next, within- and between-subject decomposition models evaluated the impact of intra- and inter-individual changes in HCQ blood levels and therapeutic HCQ blood levels on active SLE and flares over time.

resultsAt baseline visit, the mean patient age was 47 years; 91% were female, 66% were White, 45% had subtherapeutic HCQ levels (<750 ng/mL), and 79% received an HCQ dose of ≤5 mg/kg/day. Despite receiving 5 mg/kg/day, patients with kidney function ≤75 mL/min/1.73m

conclusionHCQ blood level monitoring could improve SLE control, particularly in patients with estimated glomerular filtration rate ≤75, and enable optimal HCQ use.

Identifiers

PMID41983645
PMCPMC13463390

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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.