Evidence map›Paper›PMID 40011066›Full record

Observational studyLupus science & medicine2025

Hydroxychloroquine in patients with systemic lupus erythematosus: how much is enough?

Guillermo Ruiz-Irastorza, Diana Paredes-Ruiz, Fernando Arizpe, Valerio Campos-Rodriguez, Victor Moreno-Torres, Laura Amo, Ioana Ruiz-Arruza, Daniel Martin-Iglesias

Erratum issuedAbstract readObservational Study
In one paragraph

Observational study in Lupus science & medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Observational
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Guillermo Ruiz-IrastorzaAutoimmune Diseases, Biobizkaia Health Research Institute, Barakaldo, Bizkaia, Spain guillermo.ruiz@ehu.eus.ORCID 0000-0001-7788-1043
Diana Paredes-RuizAutoimmune Diseases, Biobizkaia Health Research Institute, Barakaldo, Bizkaia, Spain.
Fernando ArizpeAutoimmune Diseases, Biobizkaia Health Research Institute, Barakaldo, Bizkaia, Spain.
Valerio Campos-RodriguezAutoimmune Diseases, Biobizkaia Health Research Institute, Barakaldo, Bizkaia, Spain.
Victor Moreno-TorresAutoimmune Diseases, Biobizkaia Health Research Institute, Barakaldo, Bizkaia, Spain.ORCID 0000-0002-9798-4514
Laura AmoAutoimmune Diseases, Biobizkaia Health Research Institute, Barakaldo, Bizkaia, Spain.
Ioana Ruiz-ArruzaAutoimmune Diseases, Biobizkaia Health Research Institute, Barakaldo, Bizkaia, Spain.
Daniel Martin-IglesiasAutoimmune Diseases, Biobizkaia Health Research Institute, Barakaldo, Bizkaia, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo assess the daily and weight-adjusted dosages of hydroxychloroquine (HCQ) and the effects on long-term remission in the Lupus-Cruces cohort.

methodsObservational study of routine clinical care data. We selected inception patients treated with HCQ with at least 5 years of follow-up. Prolonged remission was achieved when patients fulfilled definitions of remission in systemic lupus erythematosus remission criteria in five consecutive yearly visits. The associations between the weight-adjusted dose of HCQ during 5 years and prolonged remission were analysed. We also investigated the associations between prednisone doses, immunosuppressives (IS) and other antimalarial use with HCQ doses.

results150 inception patients fulfilled the inclusion criteria. The mean starting dose of HCQ was 206 mg/day. The mean weight-adjusted starting dose of HCQ was 3.1 mg/kg/day with no patients treated with doses ≥5 mg/kg/day. Treatment with HCQ was maintained during the whole 5-year follow-up time in 147 patients (98%). The mean dose of HCQ during the 5-year follow-up was 194.6 mg/day (2.9 mg/kg/day). 108 patients (72%) were in prolonged remission. The mean weight-adjusted dose of HCQ per patient did not differ between those who did and did not achieve prolonged remission (2.9 vs 3 mg/kg/day, p=0.5). The dose of prednisone per patient (mean 2.3 mg/day during the 5-year follow-up) did not differ according to the weight-adjusted dose of HCQ. The mean weight-adjusted HCQ dose during the whole follow-up was the same in patients treated or not with IS or with mepacrine.

conclusionsWith the use of HCQ at stable doses of 200 mg/day (or 3.0-3.5 mg/kg/day) as the background therapy in patients with systemic lupus erythematosus, the majority of patients achieved prolonged remission.

Indexed as

Antirheumatic AgentsHydroxychloroquineLupus Erythematosus, SystemicAdultAntimalarialsDose-Response Relationship, DrugFemaleFollow-Up StudiesHumansImmunosuppressive AgentsMaleMiddle AgedPrednisoneRemission InductionTreatment OutcomeYoung AdultAntimalarialsAntirheumatic AgentsHydroxychloroquineImmunosuppressive AgentsPrednisoneAntirheumatic AgentsGlucocorticoidsSystemic Lupus ErythematosusTherapeutics

Identifiers

PMID40011066
PMCPMC11865800

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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.