# Pituitary function in patients with primary and secondary empty sella

**Authors:** Lucas Steckel, Elke R. Gizewski, Susanne Kaser

PMC · DOI: 10.3389/fendo.2025.1632824 · Frontiers in Endocrinology · 2025-07-16

## TL;DR

The study examines pituitary function in patients with primary or secondary empty sella and finds that hormone deficiencies are common, especially in secondary cases.

## Contribution

The study provides longitudinal data on pituitary function in empty sella patients and identifies risk factors for hormone deficiencies.

## Key findings

- Hormone deficiencies were found in 34% of primary and 63.6% of secondary empty sella patients at baseline.
- Adrenal insufficiency was most common in secondary empty sella, while hypogonadism was most common in primary cases.
- Only two patients with initially normal pituitary function developed hormone deficiencies during follow-up.

## Abstract

Due to the increasing availability and sensitivity of neuroradiological imaging, the number of incidental findings of empty sella (ES) is rising, however, the clinical relevance is not clearly defined.

In this longitudinal, single-center study patients with first-time diagnosed primary or secondary empty sella were analyzed and followed up for five years. Hormone deficiencies were diagnosed by measuring basal pituitary and target organ hormone levels or dynamic stimulation tests.

Overall, 119 patients, 97 with primary (PES) and 22 with secondary empty sella (SES) were included. At baseline, isolated or total pituitary insufficiency was detected in 34% of patients with PES and 63.6% of patients with SES. While hypogonadism was the most common finding in PES affecting 25.8% of patients, adrenal insufficiency was the most frequent finding in SES affecting 54.5% of patients. Only two patients with intact pituitary function at baseline, one with SES and one with PES, were diagnosed with hormone insufficiency during follow-up.

Hormone deficiency is common in empty sella, with males and patients with SES being at highest risk. In patients with intact pituitary function at time of diagnosis, the risk of developing hypopituitarism is low thus not justifying regular follow-up assessments.

## Linked entities

- **Diseases:** hypogonadism (MONDO:0002146), adrenal insufficiency (MONDO:0000004), hypopituitarism (MONDO:0005152)

## Full-text entities

- **Genes:** GH1 (growth hormone 1) [NCBI Gene 2688] {aka GH, GH-N, GHB5, GHN, IGHD1A, IGHD1B}, POMC (proopiomelanocortin) [NCBI Gene 5443] {aka ACTH, CLIP, LPH, MSH, NPP, OBAIRH}, IGF1 (insulin like growth factor 1) [NCBI Gene 3479] {aka IGF, IGF-I, IGFI, MGF}, GGH (gamma-glutamyl hydrolase) [NCBI Gene 8836] {aka GATD10, GH}, PRL (prolactin) [NCBI Gene 5617] {aka GHA1, pPRL}
- **Diseases:** galactorrhea (MESH:D005687), collapse (MESH:D001261), traumatic brain injury (MESH:D000070642), migraine (MESH:D008881), diaphragm malformation (MESH:D065630), Weakness (MESH:D018908), skin lesions (MESH:D012871), anterior pituitary deficiency (MESH:D010900), prolactinoma (MESH:D015175), visual disturbances (MESH:D014786), PES (OMIM:192950), primary hyperparathyroidism (MESH:D049950), primary hypothyroidism (MESH:D007037), fatigue (MESH:D005221), endocrine disturbances (MESH:D004700), Arginine vasopressin deficiency (MESH:D020790), Muscle pain (MESH:D063806), Pituitary deficiency (MESH:D010911), Adrenal insufficiency (MESH:D000309), Female hypogonadotropic hypogonadism (MESH:D007006), deficiencies of the somatotropic and thyreotropic axes (MESH:D007153), Hyperprolactinemia (MESH:D006966), reduced libido (MESH:D001523), amenorrhea (MESH:D000568), Sheehan syndrome (MESH:D007018), deficiencies of the thyrotropic axis (MESH:C566610), ES (MESH:D004652), polyuria (MESH:D011141), GH deficiency (MESH:D004393), polydipsia (MESH:D059606), craniopharyngioma (MESH:D003397), Weight loss (MESH:D015431), obese (MESH:D009765)
- **Chemicals:** fT4 (-), testosterone (MESH:D013739), Arginine hydrochloride (MESH:D001120), sodium (MESH:D012964), cortisol (MESH:D006854)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12307204/full.md

## References

29 references — full list in the complete paper: https://tomesphere.com/paper/PMC12307204/full.md

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Source: https://tomesphere.com/paper/PMC12307204