# Endocrinology and the Lung: Exploring the Bidirectional Axis and Future Directions

**Authors:** Pedro Iglesias

PMC · DOI: 10.3390/jcm14196985 · 2025-10-02

## TL;DR

This review explores how the lungs interact with hormones, influencing and being influenced by endocrine systems, and highlights future research directions.

## Contribution

The paper provides a comprehensive overview of the bidirectional endocrine-pulmonary axis and its implications for disease and therapy.

## Key findings

- The lung functions as an endocrine organ, secreting hormones that affect vascular tone and immune responses.
- Endocrine diseases like Cushing’s syndrome and hypothyroidism have distinct respiratory manifestations.
- Chronic lung diseases alter endocrine axes, contributing to insulin resistance and metabolic changes.

## Abstract

The lung is increasingly recognized as an organ with dual endocrine and respiratory roles, participating in a complex bidirectional crosstalk with systemic hormones and local/paracrine activity. Endocrine and paracrine pathways regulate lung development, ventilation, immunity, and repair, while pulmonary cells express hormone receptors and secrete mediators with both local and systemic effects, defining the concept of the “endocrine lung”. This narrative review summarizes current evidence on the endocrine–pulmonary axis. Thyroid hormones, glucocorticoids, sex steroids, and metabolic hormones (e.g., insulin, leptin, adiponectin) critically influence alveologenesis, surfactant production, ventilatory drive, airway mechanics, and immune responses. Conversely, the lung produces mediators such as serotonin, calcitonin gene-related peptide, endothelin-1, leptin, and keratinocyte growth factor, which regulate vascular tone, alveolar homeostasis, and immune modulation. We also describe the respiratory manifestations of major endocrine diseases, including obstructive sleep apnea and lung volume alterations in acromegaly, immunosuppression and myopathy in Cushing’s syndrome, hypoventilation in hypothyroidism, restrictive “diabetic lung”, and obesity-related phenotypes. In parallel, chronic pulmonary diseases such as chronic obstructive pulmonary disease, interstitial lung disease, and sleep apnea profoundly affect endocrine axes, promoting insulin resistance, hypogonadism, GH/IGF-1 suppression, and bone metabolism alterations. Pulmonary neuroendocrine tumors further highlight the interface, frequently presenting with paraneoplastic endocrine syndromes. Finally, therapeutic interactions are discussed, including the risks of hypothalamic–pituitary–adrenal axis suppression with inhaled corticosteroids, immunotherapy-induced endocrinopathies, and inhaled insulin. Future perspectives emphasize mapping pulmonary hormone networks, endocrine phenotyping of chronic respiratory diseases, and developing hormone-based interventions.

## Linked entities

- **Proteins:** lepa (leptin a)
- **Chemicals:** insulin (PubChem CID 70678557), leptin (PubChem CID 157010069)
- **Diseases:** obstructive sleep apnea (MONDO:0007147), acromegaly (MONDO:0019933), Cushing’s syndrome (MONDO:0018912), hypothyroidism (MONDO:0005420), chronic obstructive pulmonary disease (MONDO:0005002), interstitial lung disease (MONDO:0015925), sleep apnea (MONDO:0005296)

## Full-text entities

- **Genes:** INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, LEP (leptin) [NCBI Gene 3952] {aka LEPD, OB, OBS}, FGF7 (fibroblast growth factor 7) [NCBI Gene 2252] {aka HBGF-7, KGF}, EDN1 (endothelin 1) [NCBI Gene 1906] {aka ARCND3, ET1, HDLCQ7, PPET1, QME}, GGH (gamma-glutamyl hydrolase) [NCBI Gene 8836] {aka GATD10, GH}, ADIPOQ (adiponectin, C1Q and collagen domain containing) [NCBI Gene 9370] {aka ACDC, ACRP30, ADIPQTL1, ADPN, APM-1, APM1}, IGF1 (insulin like growth factor 1) [NCBI Gene 3479] {aka IGF, IGF-I, IGFI, MGF}
- **Diseases:** chronic obstructive pulmonary disease (MESH:D029424), Cushing's syndrome (MESH:D003480), Pulmonary neuroendocrine tumors (MESH:D018358), endocrinopathies (MESH:C567425), hypogonadism (MESH:D007006), interstitial lung disease (MESH:D017563), hypoventilation (MESH:D007040), diabetic lung (MESH:D003920), acromegaly (MESH:D000172), obstructive sleep apnea (MESH:D020181), respiratory diseases (MESH:D012140), hypothyroidism (MESH:D007037), insulin resistance (MESH:D007333), endocrine diseases (MESH:D004700), obesity (MESH:D009765), paraneoplastic endocrine syndromes (MESH:D009384), chronic pulmonary diseases (MESH:D002908), myopathy (MESH:D009135), sleep apnea (MESH:D012891)
- **Chemicals:** serotonin (MESH:D012701)

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12525173/full.md

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Source: https://tomesphere.com/paper/PMC12525173