Evidence map›Paper›PMID 30201849›Full record

Trial reportDiabetes care2018

Combined Immunosuppressive Therapy Induces Remission in Patients With Severe Type B Insulin Resistance: A Prospective Cohort Study.

Joanna Klubo-Gwiezdzinska, Maria Lange, Elaine Cochran, Robert K Semple, Cornelia Gewert, Rebecca J Brown, Phillip Gorden

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in Diabetes care, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.8field-weighted citation impact, top 7% of its field
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

28 citing papers in PubMed, 39 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
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  8. Review
  9. Article
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  11. Article
  12. Article
  13. Syndromes of autoantibodies to the insulin receptor.International journal of biochemistry and molecular biology · 2022
    Article
  14. Article
  15. Review
  16. Article
  17. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 2 countries.

Joanna Klubo-GwiezdzinskaMetabolic Disease Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD joanna.klubo-gwiezdzinska@nih.gov.ORCID 0000-0001-8633-4420
Maria LangeSchool of Medicine, Dentistry and Nursing, University of Glasgow, Glasgow, U.K.
Elaine CochranDiabetes, Endocrinology and Obesity Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD.
Robert K SempleUniversity of Edinburgh, Edinburgh, U.K.ORCID 0000-0001-6539-3069
Cornelia GewertUniversity of Cambridge, Cambridge, U.K.
Rebecca J BrownDiabetes, Endocrinology and Obesity Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD.
Phillip GordenDiabetes, Endocrinology and Obesity Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD.
National Institutes of Health · USUniversity of Cambridge · GBUniversity of Edinburgh · GBUniversity of Glasgow · GB

Funding

Studies of Thyroid Function in Health and DiseaseZIEDK075005 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI KLUBO-GWIEZDZINSKA, JOANNA · 2013 to 2024
$2.3M
Wellcome Trust 210752/Z/18/Z
6 · The paper itself

Abstract

objectiveType B insulin resistance due to autoantibodies against the insulin receptor is characterized by diabetes refractory to massive doses of insulin, severe hypercatabolism, hyperandrogenism, and a high mortality rate. We analyzed the efficacy of combined immunosuppressive therapy in the management of this extreme form of diabetes. RESEARCH DESIGN AND

methodsWe performed a prospective cohort study including patients with confirmed insulin receptor autoantibodies, monitored for median 72 months (25th, 75th interquartile range 25, 88), and treated with rituximab, high-dose pulsed steroids, and cyclophosphamide until remission, followed by maintenance therapy with azathioprine. Remission was defined as the amelioration of the hyperglycemia and discontinuation of insulin and/or normalization of hyperandrogenemia.

resultsAll data are given as median (25th, 75th interquartile range). Twenty-two patients aged 42 (25, 57) years, 86.4% women, fulfilled inclusion criteria. At baseline, fasting glucose was 307 (203, 398) mg/dL, HbA

conclusionsCombined immunosuppressive therapy has changed the natural history of this disease, from 54% mortality to a curable form of diabetes and, as such, should be recommended in patients with type B insulin resistance.

Indexed as

Insulin ResistanceAdultAntigens, CDAutoantibodiesAzathioprineCohort StudiesCyclophosphamideDexamethasoneDiabetes Mellitus, Type 1Drug Therapy, CombinationFemaleFollow-Up StudiesHumansHyperglycemiaImmunosuppressive AgentsInsulinAntigens, CDAutoantibodiesAzathioprineCyclophosphamideDexamethasoneImmunosuppressive AgentsINSR protein, humanInsulinMethylprednisoloneReceptor, InsulinRituximab

Identifiers

PMID30201849
PMCPMC6196834
OpenAlexW2891959577

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.