Evidence map›Paper›PMID 42116187›Full record

ArticleArthritis research & therapy2026

Clinical characteristics and response to standard-of-care treatment in systemic lupus erythematosus patients with or without anti-ribonucleoprotein (RNP) antibodies: an Australian, multi-centre cohort study.

Rangi Kandane-Rathnayake, Rachel Koelmeyer, Shereen Oon, Maureen Rischmueller, Yumi Oh, Sean O'Neill, Geraldine Hassett, Sachin Khetan, Ted Tsai, Fiona Goldblatt and 8 more

Abstract readMulticenter Study
In one paragraph

Article in Arthritis research & therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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5 · Who and what money

Authors and funding

18 authors.

Rangi Kandane-RathnayakeCentre for Inflammatory Diseases, Monash University, Clayton, VIC, Australia. rangi.kandane-rathnayake@monash.edu.ORCID http://orcid.org/0000-0001-5397-1482
Rachel KoelmeyerCentre for Inflammatory Diseases, Monash University, Clayton, VIC, Australia.
Shereen OonDepartment of Rheumatology, St Vincent's Hospital Melbourne, Fitzroy, VIC, Australia.
Maureen RischmuellerDepartment of Rheumatology, The Queen Elizabeth Hospital, University of Adelaide, Adelaide, SA, Australia.
Yumi OhDepartment of Rheumatology, Redcliffe Hospital, Redcliffe, QLD, Australia.
Sean O'NeillDepartment of Rheumatology, Liverpool Hospital, Liverpool, NSW, Australia.
Geraldine HassettDepartment of Rheumatology, Liverpool Hospital, Liverpool, NSW, Australia.
Sachin KhetanDepartment of Rheumatology, Royal Darwin Hospital, Tiwi, NT, Australia.
Ted TsaiDepartment of Rheumatology, Canberra Hospital, Garran, ACT, Australia.
Fiona GoldblattDepartment of Rheumatology, Flinders Medical Centre, Bedford Park, SA, Australia.
Ashleigh HennesseyDepartment of Rheumatology, Royal Brisbane and Women's Hospital & University of Queensland, Brisbane, QLD, Australia.
Dwarakanathan RanganathanDepartment of Kidney Health Services, Metro North Hospital and Health Services, School of Medicine and Dentistry, Griffith University, Griffith, QLD, Australia.
Adrienne LefeberNovartis Pharmaceuticals, Cambridge, MA, US.
Tamas ShishaNovartis Pharmaceuticals, Basel, Switzerland.
Peter GergelyNovartis Pharmaceuticals, Basel, Switzerland.
Mandana NikpourDepartment of Rheumatology, St Vincent's Hospital Melbourne, Fitzroy, VIC, Australia.
Eric MorandCentre for Inflammatory Diseases, Monash University, Clayton, VIC, Australia.
Alberta HoiCentre for Inflammatory Diseases, Monash University, Clayton, VIC, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAnti-ribonucleoprotein (RNP) (auto)antibodies are frequently detected in patients with systemic lupus erythematosus (SLE) although their associations with SLE disease activity remain incompletely understood. We compared patient characteristics, including disease severity outcomes, between adult patients with SLE with or without anti-RNP antibodies (RNP + versus RNP-).

methodsWe used data from a national, multicentre registry of SLE patients in Australia, collected prospectively between 2007 and 2023. Anti-RNP status and other serological profiles along with demographics were recorded at enrolment. At each routine clinic visit, medication details and disease activity indicators (SLEDAI-2 K, PGA) were captured, and treat-to-target (T2T) states, lupus low disease activity state (LLDAS) and DORIS remission (REM), were determined. Clinical characteristics were compared between RNP + and RNP- patients at 6 months (182 ± 30 days) and 12 months (365 ± 30 days) from enrolment.

resultsA total of 587 patients were studied. 174 (29.6% (95%CI: 26.1%, 33.4%)) were RNP + with significantly higher disease activity and more medication use at enrolment compared with RNP- patients (SLEDAI-2 K median [IQR]: 8.0 [4.0, 10.0] versus 4.0 [2.0, 8.0], p < 0.001; PGA: 0.9 [0.4, 1.2] versus 0.5 [0.2, 1.0], p < 0.001; daily glucocorticoid dose 6.8 [0.0, 15.0] versus 3.0 [0.0, 10.0] mg/day, p < 0.001). RNP + group had more patients with renal, cutaneous, and serological activity. At enrolment, a greater proportion of RNP + patients had active disease (SLEDAI-2 K ≥ 6) compared with RNP- patients (53% versus 41%, p < 0.007), whereas significantly fewer RNP + patients were in LLDAS (20% versus 32.2%, p-value = 0.004) or REM (11.6% versus 22.6%, p-value = 0.006). RNP + patients were 18-fold more likely to be positive for anti-Sm antibodies, and associations with disease activity attenuated upon adjustment for this, though highest disease activity was observed in patients positive to both anti-RNP and anti-Sm autoantibodies (RNP + Sm +). Disease activity indicators between RNP + and RNP- groups converged within the first 12 months following enrolment. Glucocorticoid and immunosuppressant use remained significantly higher in RNP + Sm + patients.

conclusionsAnti-RNP positive patients presented with a higher burden of disease activity, and required more intensive treatment with glucocorticoids and immunosuppressants during the first year since study of follow-up, but this was largely driven by the strong association of anti-RNP positivity with anti-Sm positivity.

Indexed as

Antibodies, AntinuclearAutoantibodiesLupus Erythematosus, SystemicRibonucleoproteinsStandard of CareAdultAustraliaCohort StudiesFemaleHumansMaleMiddle AgedProspective StudiesRegistriesSeverity of Illness IndexTreatment OutcomeAntibodies, AntinuclearAutoantibodiesRibonucleoproteinsAnti-RNP autoantibodiesCohort studyDisease activitySLEStandard of care

Identifiers

PMID42116187
PMCPMC13330039

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Registered trials

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