ArticleAnnals of hematology2026
Clinical utility of copeptin in histiocytosis-associated arginine vasopressin deficiency: a report of three cases.
Article in Annals of hematology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
9 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Arginine vasopressin deficiency (AVP-D) is a frequent complication of histiocytosis and may precede the systemic manifestations of the disease of several years. Currently, no reliable biomarkers allow the diagnosis of AVP-D in the setting of histiocytosis. Traditional diagnostic methods, such as the water deprivation test, are often impractical. Copeptin, a new surrogate marker for arginine vasopressin, has been used for the diagnosis of AVP-D in other conditions, such as trauma and malignancies. We herein report three clinical cases of systemic histiocytosis (one Erdheim-Chester disease, one Rosai-Dorfman-Destombes disease, and one Langerhans cell histiocytosis) where plasma copeptin was utilized to identify AVP-D. The three cases differed not only because of the underlying diagnosis, but also in terms of clinical characteristics and rapidity of onset of AVP-D. We propose an early integration of copeptin into the diagnostic workup of systemic histiocytosis.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.