# Impact of a Hypocaloric Diet on Prognostic Biomarkers of Endothelial Dysfunction: A Prospective Study

**Authors:** Cristina Lazar, Minela Aida Maranduca, Cristian Tudor Cozma, Andreea Clim, Mihaela Moscalu, Dragomir-Nicolae Serban, Ionela-Lacramioara Serban

PMC · DOI: 10.3390/jcm15062321 · Journal of Clinical Medicine · 2026-03-18

## TL;DR

A new biomarker called ACLI was developed to assess atherogenic risk in overweight and obese individuals, and it improved after a calorie-restricted diet.

## Contribution

The study introduces and validates ACLI as a novel biomarker for atherogenic burden and its link to inflammation.

## Key findings

- ACLI significantly decreased after a six-month hypocaloric diet and correlated with inflammatory markers like hs-CRP and IL-6.
- ACLI showed better discrimination of inflammatory status than traditional atherogenic indices like AIP, CRI–1, and CRI–2.

## Abstract

Background/Objectives: To assess the impact of weight loss on the atherogenic profile of patients with obesity, we proposed the Atherogenic Central Load Index (ACLI). The aim of the study was to validate ACLI as a novel lipid biomarker reflecting the balance between atherogenic and antiatherogenic lipoproteins, the overall atherogenic burden, and its association with inflammatory markers. Methods: A prospective study was conducted from January 2024 to July 2024. A total of 73 adults with overweight or obesity completed a six-month dietary-based weight loss intervention. A 15% caloric deficit target was set, excluding the potential influence of pharmacotherapy, and limiting physical activity to daily walking. Statistical analysis focused on anthropometric measures, lipid panel parameters and derived atherosclerosis indices. Results: The intervention returned a median weight loss of 11.8 (IQR: 8–19) kg. Before–after analysis showed a statistically significant improvement in anthropometric indices and most lipid profile components. To assess the effect of weight loss on the atherogenic profile of patients, we proposed an atherogenic load index (Atherogenic Central Load Index (ACLI)). ACLI decreased significantly following the hypocaloric diet and showed a significant correlation with the inflammatory markers hs-CRP and IL-6. ACLI showed a strong, inversely significant correlation (p < 0.05) with AIP, hs-CRP and IL-6, at the time of intervention initiation and after 6 months. The evaluation of the obtained AUC values allowed to clearly highlight the superior discrimination performance of ACLI regarding the inflammatory markers hs-CRP and IL-6 in patients with overweight and obesity involved in dietary interventions for weight loss. Conclusions. The proposed index (ACLI) showed strong and significant associations with key inflammatory markers, including hs-CRP and IL-6. Moreover, ACLI demonstrated superior discriminatory performance for elevated inflammatory status in overweight and individuals with obesity undergoing dietary weight-loss interventions, outperforming traditional atherogenic indices related to atherosclerosis progression (AIP, CRI–1, and CRI–2). These findings support the potential clinical utility of ACLI as an integrative marker of atherogenic burden and cardiometabolic risk.

## Linked entities

- **Diseases:** obesity (MONDO:0011122), atherosclerosis (MONDO:0005311)

## Full-text entities

- **Genes:** AIP (AHR interacting HSP90 co-chaperone) [NCBI Gene 9049] {aka ARA9, FKBP16, FKBP37, PITA1, SMTPHN, XAP-2}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}
- **Diseases:** caloric deficit (MESH:D009461), inflammatory (MESH:D007249), Endothelial Dysfunction (MESH:D014652), Atherogenic (MESH:D050197), weight loss (MESH:D015431), obesity (MESH:D009765), overweight (MESH:D050177)
- **Chemicals:** lipid (MESH:D008055)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13026628/full.md

## References

54 references — full list in the complete paper: https://tomesphere.com/paper/PMC13026628/full.md

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Source: https://tomesphere.com/paper/PMC13026628