# Association of hippocampus, entorhinal cortex, and amygdala with thyroid function: a bilateral volumetric analysis

**Authors:** Asma Hallab

PMC · DOI: 10.1186/s13044-026-00289-4 · Thyroid Research · 2026-02-23

## TL;DR

This study explores how thyroid function relates to brain structures like the hippocampus and entorhinal cortex in older adults.

## Contribution

The study reveals sex- and cognition-specific associations between thyroid hormone levels and brain volume in aging populations.

## Key findings

- Lower TSH levels were associated with lower left hippocampus volume in MCI.
- Lower TSH levels were associated with lower left entorhinal cortex volume in MCI.
- No significant association between TSH and bilateral amygdala volumes was observed.

## Abstract

Thyroid hormones modulate brain structures during neurogenesis and impact cognition and emotions during the lifetime. Hypothyroidism is commonly associated with lower gray matter volume. Fewer studies, however, highlighted significant associations between higher thyroid function and cognitive impairment. Aging is an independent risk factor for cognitive decline and thyroid dysfunction. It is, therefore, important to understand the association of thyroid function with relevant brain structures during the aging process. A subset of 1,010 adults (≥ 50 years) from the Alzheimer’s Disease Neuroimaging Initiative (ADNI) was included. Multivariable linear regression was used. Comparative bilateral volumetric analyses and interaction-based cognition-related stratifications were performed. Females represented 50.00% of included cases, and 43.50% were healthy controls (HC). Thyroid Stimulating Hormone (TSH) levels were lower in the mild cognitive impairment (MCI) group (1.67 vs. 1.81 µIU/mL, p-value = 0.024). A significant positive association between TSH (µIU/mL) and left hippocampus volume (mm3) was found in MCI (adj.ß=44.00 [7.50, 81.00], p-value = 0.018). Similar results were found in the right hippocampus, but only in the total study population (adj.ß=29.00 [4.00, 54.00], p-value = 0.023). There was a significant association between TSH (µIU/mL) and left EC volume (mm3) in the total study population (adj.ß=31.00 [9.40, 52.00], p-value = 0.005), and after stratification, this association remained statistically significant only in MCI (adj.ß=54.00 [24.00, 84.00], p-value < 0.001). The association between TSH and the amygdala was not statistically significant. It is, therefore, crucial to consider the role of cognitive status and laterality when exploring the thyroid-brain interaction in older adults.

The online version contains supplementary material available at 10.1186/s13044-026-00289-4.

Not applicable.

The online version contains supplementary material available at 10.1186/s13044-026-00289-4.

Lower TSH levels were associated with lower left hippocampus volume in MCI.

Lower TSH levels were associated with lower left entorhinal cortex volume in MCI.

No significant association between TSH and bilateral amygdala volumes was observed.

The online version contains supplementary material available at 10.1186/s13044-026-00289-4.

## Linked entities

- **Diseases:** hypothyroidism (MONDO:0005420)

## Full-text entities

- **Genes:** CAMK2G (calcium/calmodulin dependent protein kinase II gamma) [NCBI Gene 818] {aka CAMK, CAMK-II, CAMKG, MRD59}, APOE (apolipoprotein E) [NCBI Gene 348] {aka AD2, APO-E, ApoE4, LDLCQ5, LPG}, MAPT (microtubule associated protein tau) [NCBI Gene 4137] {aka DDPAC, FTD1, FTDP-17, MAPTL, MSTD, MTBT1}, TSHR (thyroid stimulating hormone receptor) [NCBI Gene 7253] {aka CHNG1, LGR3, hTSHR-I}
- **Diseases:** neurodegeneration (MESH:D019636), volume loss (MESH:D016388), HC (MESH:D000067329), GDS (MESH:C538175), amyloid-ss toxicity (MESH:D000080822), neuropsychiatric symptoms (MESH:D001523), MCI (MESH:D060825), ADNI (MESH:D000544), EC (MESH:D000303), atrophy (MESH:D001284), Anxiety (MESH:D001007), affective disorders (MESH:D019964), Hyperthyroidism (MESH:D006980), thyroid (dys)function (MESH:D013966), Graves' disease (MESH:D006111), hippocampal (MESH:D000092223), Hypothyroidism (MESH:D007037), congenital hypothyroidism (MESH:D003409), psychosis (MESH:D011618), neuropsychiatric (MESH:C000631768), thyroid dysfunction (MESH:D013959), Depression (MESH:D003866), bipolar disorder (MESH:D001714), Dysfunction in the amygdalae (MESH:D006331), thyrotoxicosis (MESH:C566386), amyloid (MESH:C000718787), Dementia (MESH:D003704), cognitive adversities (MESH:D003072)
- **Chemicals:** L-T4 (MESH:D013974), FT3 (-), iodine (MESH:D007455), triiodothyronine (MESH:D014284)
- **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/PMC12927246/full.md

## References

4 references — full list in the complete paper: https://tomesphere.com/paper/PMC12927246/full.md

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Source: https://tomesphere.com/paper/PMC12927246