# Follistatin as a Potential Biomarker for Identifying Metabolically Healthy and Unhealthy Obesity: A Cross-Sectional Study

**Authors:** Ayşe N. Erbakan, H. Hicran Mutlu, Mehmet Uzunlulu, Lütfullah Caştur, Muhammet Mikdat Akbaş, Fatoş N. Kaya, Mehmet Erbakan, Ferruh K. İşman, Aytekin Oğuz

PMC · DOI: 10.3390/jpm14050487 · 2024-05-03

## TL;DR

This study explores whether follistatin can help identify metabolically healthy versus unhealthy obesity, but finds it is not a useful biomarker.

## Contribution

The study evaluates follistatin as a potential biomarker for distinguishing metabolically healthy and unhealthy obesity for the first time in this context.

## Key findings

- Follistatin levels did not significantly differ between metabolically healthy and unhealthy obese individuals.
- Insulin was the strongest predictor of follistatin levels, followed by C-peptide.
- Quantile regression revealed complex associations between follistatin and metabolic parameters.

## Abstract

Metabolically healthy obesity (MHO) refers to obese individuals with a favorable metabolic profile, without severe metabolic abnormalities. This study aimed to investigate the potential of follistatin, a regulator of metabolic balance, as a biomarker to distinguish between metabolically healthy and unhealthy obesity. This cross-sectional study included 30 metabolically healthy and 32 metabolically unhealthy individuals with obesity. Blood samples were collected to measure the follistatin levels using an enzyme-linked immunosorbent assay (ELISA). While follistatin did not significantly differentiate between metabolically healthy (median 41.84 [IQR, 37.68 to 80.09]) and unhealthy (median 42.44 [IQR, 39.54 to 82.55]) individuals with obesity (p = 0.642), other biochemical markers, such as HDL cholesterol, triglycerides, C-peptide, and AST, showed significant differences between the two groups. Insulin was the most significant predictor of follistatin levels, with a coefficient of 0.903, followed by C-peptide, which exerted a negative influence at −0.624. Quantile regression analysis revealed nuanced associations between the follistatin levels and metabolic parameters in different quantiles. Although follistatin may not serve as a biomarker for identifying MHO and metabolically unhealthy obesity, understanding the underlying mechanisms that contribute to metabolic dysfunction could provide personalized strategies for managing obesity and preventing associated complications.

## Linked entities

- **Proteins:** LOC5564573 (agrin)
- **Diseases:** obesity (MONDO:0011122)

## Full-text entities

- **Genes:** INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, FST (follistatin) [NCBI Gene 10468] {aka FS}
- **Diseases:** Obesity (MESH:D009765), MHO (MESH:D000067329), metabolic abnormalities (MESH:D008659)
- **Chemicals:** cholesterol (MESH:D002784), C-peptide (MESH:D002096), triglycerides (MESH:D014280)

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC11122067/full.md

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Source: https://tomesphere.com/paper/PMC11122067