Evidence map›Paper›PMID 37818852›Full record

ArticleEuropean journal of endocrinology2023

Resolution of dysglycaemia after treatment of monoclonal gammopathy of endocrine significance.

Bonnie Grant, Gowri Ratnayake, Claire L Williams, Anna Long, David J Halsall, Robert K Semple, James D Cavenagh, William M Drake, David S Church

Open access · hybridAbstract readCase Reports
In one paragraph

Article in European journal of endocrinology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 29% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Review
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

9 authors at 4 institutions in 1 country.

Bonnie GrantDepartment of Endocrinology, St Bartholomew's Hospital, Barts Health NHS Trust, London EC1A 7BE, United Kingdom.ORCID 0000-0003-1121-9211
Gowri RatnayakeDepartment of Endocrinology, St Bartholomew's Hospital, Barts Health NHS Trust, London EC1A 7BE, United Kingdom.
Claire L WilliamsTranslational Health Sciences, Bristol Medical School, University of Bristol, Learning and Research, Southmead Hospital, Bristol BS10 5NB, United Kingdom.
Anna LongTranslational Health Sciences, Bristol Medical School, University of Bristol, Learning and Research, Southmead Hospital, Bristol BS10 5NB, United Kingdom.ORCID 0000-0002-6847-2771
David J HalsallDepartment of Clinical Biochemistry and Immunology, Cambridge University Hospitals NHS Foundation Trust, Cambridge CB2 0QQ, United Kingdom.
Robert K SempleCentre for Cardiovascular Science, Queen's Medical Research Institute, University of Edinburgh, Edinburgh EH16 4TJ, United Kingdom.ORCID 0000-0001-6539-3069
James D CavenaghDepartment of Haematolo-Oncology, St Bartholomew's Hospital, Barts Health NHS Trust, London EC1A 7BE, United Kingdom.
William M DrakeDepartment of Endocrinology, St Bartholomew's Hospital, Barts Health NHS Trust, London EC1A 7BE, United Kingdom.
David S ChurchDepartment of Clinical Biochemistry and Immunology, Cambridge University Hospitals NHS Foundation Trust, Cambridge CB2 0QQ, United Kingdom.ORCID 0000-0002-2489-4788
St Bartholomew's Hospital · GBCambridge University Hospitals NHS Foundation Trust · GBSouthmead Hospital · GBInstitute of Genetics and Cancer · GB

Funding

Wellcome TrustWellcome Trust 210752/Z/18/Z
6 · The paper itself

Abstract

In very rare cases of monoclonal gammopathy, insulin-binding paraprotein can cause disabling hypoglycaemia. We report a 67-year-old man re-evaluated for hyperinsulinaemic hypoglycaemia that persisted despite distal pancreatectomy. He had no medical history of diabetes mellitus or autoimmune disease but was being monitored for an IgG kappa monoclonal gammopathy of undetermined significance. On glucose tolerance testing, hyperglycaemia occurred at 60 min (glucose 216 mg/dL) and hypoglycaemia at 300 min (52 mg/dL) concurrent with an apparent plasma insulin concentration of 52 850 pmol/L on immunoassay. Laboratory investigation revealed an IgG2 kappa with very high binding capacity but low affinity (Kd 1.43 × 10-6 mol/L) for insulin. The monoclonal gammopathy was restaged as smouldering myeloma not warranting plasma cell-directed therapy from a haematological standpoint. Plasma exchange reduced paraprotein levels and improved fasting capillary glucose concentrations. Lenalidomide was used to treat disabling hypoglycaemia, successfully depleting paraprotein and leading to resolution of symptoms.

Indexed as

Endocrine System DiseasesHypoglycemiaMonoclonal Gammopathy of Undetermined SignificanceMultiple MyelomaParaproteinemiasAgedGlucoseHumansInsulinMaleParaproteinsGlucoseInsulinParaproteinshyperinsulinaemiahypoglycaemiainsulin autoantibodieslenalidomideMGUSmyelomaplasma exchangesmouldering myeloma

Identifiers

PMID37818852
PMCPMC10711369
OpenAlexW4387531055

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.