ArticleCureus2025
Autoimmune Hypophysitis: A Cause of Central Diabetes Insipidus.
Article in Cureus, 2025. 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.
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Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Diabetes insipidus (DI) is a rare disorder characterized by polyuria and polydipsia due to a deficiency of antidiuretic hormone (ADH) or insensitivity to ADH. This case report presents a rare cause of DI secondary to autoimmune hypophysitis, emphasizing the diagnostic and management challenges associated with the condition. The discussion highlights pathophysiology, clinical presentation, diagnostic approaches, and therapeutic strategies. The importance of considering autoimmune hypophysitis in the differential diagnosis of central DI is underscored, along with long-term implications of the disease.
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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.