# Deciphering the Presence of Active Interscapular Brown Adipose Tissue in Humans

**Authors:** Joaquin Sanchez‐Gomez, Samuel Ruiz‐Campos, Anabel Chica‐Perez, Andrés Baena‐Raya, Francisco M. Acosta, Christian Wolfrum, Patrick C. N. Rensen, Tania Romacho, Borja Martinez‐Tellez

PMC · DOI: 10.1111/apha.70190 · 2026-03-18

## TL;DR

This review explores whether active interscapular brown adipose tissue exists in adult humans, based on anatomical, imaging, and molecular evidence.

## Contribution

The paper synthesizes evidence for the potential persistence of interscapular brown adipose tissue in adult humans, particularly in women.

## Key findings

- Dorsocervical subcutaneous adipose tissue in human neonates has been conclusively identified as interscapular brown adipose tissue.
- Cold-induced PET/CT studies show elevated glucose uptake in the dorsocervical region, more prevalent in women.
- Molecular confirmation of interscapular brown adipose tissue in adults remains lacking despite suggestive histological and imaging data.

## Abstract

Brown adipose tissue (BAT) is increasingly recognized as a metabolically active tissue in humans, although its physiological relevance remains incompletely understood. In rodents, BAT is well characterized, with interscapular BAT (iBAT) representing the main thermogenic depot. In contrast, the existence and persistence of iBAT in adult humans have long been overlooked. In this review, we synthesize anatomical, histological, imaging, and molecular evidence supporting the presence of a potentially active iBAT depot within the dorsocervical subcutaneous adipose tissue in humans. Gene expression and histological studies have conclusively identified dorsocervical subcutaneous adipose tissue as iBAT in human neonates. In adults, the persistence of this depot has been suggested by early histological observations, although definitive molecular confirmation is still lacking. More recent data from HIV‐1‐infected individuals report increased expression of BAT‐related markers in the dorsocervical region; however, histological analyses have not consistently confirmed the presence of iBAT in this population. In parallel, two independent cold‐induced 18F‐FDG‐PET/CT studies have reported elevated glucose uptake in this area, with a higher prevalence in women. Taken together, these findings suggest that a dorsocervical subcutaneous adipose depot with BAT‐like characteristics may persist into adulthood, particularly in women. Nevertheless, targeted biopsy studies combined with molecular and cellular analyses, together with advanced PET‐CT imaging using tracers capable of assessing thermogenic activity in vivo, are required to clarify whether this tissue represents classical BAT, a beige adipose depot, or a developmentally retained adipose niche. Defining the identity and function of this depot would advance current concepts of human adipose tissue heterogeneity.

## Full-text entities

- **Genes:** ZIC1 (Zic family zinc finger 1) [NCBI Gene 7545] {aka BAIDCS, CRS6, ZIC, ZNF201}, LEP (leptin) [NCBI Gene 3952] {aka LEPD, OB, OBS}, PPARGC1A (PPARG coactivator 1 alpha) [NCBI Gene 10891] {aka LEM6, PGC-1(alpha), PGC-1alpha, PGC-1v, PGC1, PGC1A}, DIO2 (iodothyronine deiodinase 2) [NCBI Gene 1734] {aka 5DII, D2, DIOII, SELENOY, SelY, TXDI2}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, UCP1 (uncoupling protein 1) [NCBI Gene 7350] {aka SLC25A7, UCP}, TBX1 (T-box transcription factor 1) [NCBI Gene 6899] {aka CAFS, CATCH22, CTHM, DGCR, DGS, DORV}, LMNA (lamin A/C) [NCBI Gene 4000] {aka CDCD1, CDDC, CMD1A, CMT2B1, EMD2, FPL}, SLC10A2 (solute carrier family 10 member 2) [NCBI Gene 6555] {aka ASBT, IBAT, ISBT, NTCP2, PBAM, PBAM1}, BAAT (bile acid-CoA:amino acid N-acyltransferase) [NCBI Gene 570] {aka BACAT, BACD1, BAT, FHCA3, HCHO}
- **Diseases:** Diabetes (MESH:D003920), neck cancer (MESH:D006258), HALS (MESH:D016609), adipocyte hyperplasia (MESH:D006965), MHO (MESH:D000067329), lipomatous (MESH:D008080), inflammatory (MESH:D007249), buffalo hump lipomatosis (MESH:D008068), lipomas (MESH:D008067), hypertrophy (MESH:D006984), cardiometabolic complications (MESH:D024821), overweight (MESH:D050177), Digestive and Kidney Diseases (MESH:D007674), fibrosis (MESH:D005355), lipodystrophy (MESH:D008060), obesity (MESH:D009765), cancer (MESH:D009369), dystrophy (MESH:D058499), lipoatrophy (MESH:C535905), HIV (MESH:D015658)
- **Chemicals:** triglycerides (MESH:D014280), H2O (MESH:D014867), Glucose (MESH:D005947), lipid (MESH:D008055), eosin (MESH:D004801), hematoxylin (MESH:D006416), 18F FDG (MESH:D019788), oxygen (MESH:D010100), calcium (MESH:D002118), 15O2 (-), paraffin (MESH:D010232), creatine (MESH:D003401), 11C-acetate (MESH:C438206)
- **Species:** Homo sapiens (human, species) [taxon 9606], Human immunodeficiency virus 1 (no rank) [taxon 11676], Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** H-Ad-3 — Homo sapiens (Human), Plasma cell myeloma, Cancer cell line (CVCL_A634)

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12998703/full.md

---
Source: https://tomesphere.com/paper/PMC12998703