Cardiovascular

STOP-BANG-Defined high OSA risk is associated with left ventricular diastolic dysfunction in obese adults.

TL;DR

In obese adults, STOP-BANG-defined high OSA risk is associated with a phenotype characterized by greater epicardial adiposity, higher inflammatory burden, autonomic impairment, and a higher prevalence of left ventricular diastolic dysfunction.

Key Findings

Left ventricular diastolic dysfunction was substantially more prevalent in obese participants than in non-obese controls.

  • LVDD prevalence was 43% in obese participants versus 7% in non-obese controls (p < 0.001).
  • The study included 113 obese adults (BMI ≥ 30 kg/m²) and 166 non-obese controls (BMI < 25 kg/m²), totaling 279 participants.
  • LVDD was assessed by transthoracic echocardiography according to the 2016 ASE/EACVI recommendations.
  • This was a single-center, cross-sectional study of consecutive adult patients presenting to a cardiology outpatient clinic between January and December 2025.

High STOP-BANG risk (score ≥ 3) remained independently associated with LVDD in multivariable analyses restricted to obese participants.

  • In the full multivariable model, high STOP-BANG risk was associated with LVDD with an OR of 2.67 (95% CI 1.25–5.71; p = 0.011).
  • In the reduced multivariable model, the association persisted with an OR of 2.55 (95% CI 1.31–5.55; p = 0.011).
  • OSA risk was evaluated using the STOP-BANG questionnaire, with high risk prespecified as a score ≥ 3.
  • Multivariable analyses were prespecified and restricted to obese participants with definitive diastolic classification.

Within the obese subgroup, high STOP-BANG risk was associated with greater epicardial adipose tissue thickness.

  • Epicardial adipose tissue (EAT) thickness was measured as part of the study protocol.
  • High STOP-BANG risk (≥ 3) was associated with greater EAT thickness compared to obese participants with low STOP-BANG risk.
  • EAT thickness was included as one of three components in the reduced screening-oriented model for LVDD discrimination.

High STOP-BANG risk in obese adults was associated with higher systemic inflammatory burden as measured by NLR and SII.

  • Inflammatory indices measured included the neutrophil-to-lymphocyte ratio (NLR) and the systemic immune-inflammation index (SII).
  • Obese participants with high STOP-BANG risk had higher inflammatory indices compared to those with low STOP-BANG risk.
  • Inflammatory indices were included alongside STOP-BANG category and EAT thickness in the screening-oriented discriminative model.

High STOP-BANG risk in obese adults was associated with lower heart rate variability indices, indicating autonomic impairment.

  • HRV parameters were analyzed as supportive mechanistic markers only, not as primary endpoints.
  • Obese participants with high STOP-BANG risk demonstrated lower HRV indices compared to those with low STOP-BANG risk.
  • The authors described this as consistent with autonomic imbalance coexisting with epicardial adiposity and systemic inflammation in the high-risk OSA phenotype.

A reduced screening-oriented model incorporating STOP-BANG category, EAT thickness, and inflammatory indices showed acceptable discrimination for LVDD in obese adults.

  • The parsimonious model integrated three components: STOP-BANG category, EAT thickness, and inflammatory indices.
  • The model was described as showing 'acceptable discrimination' for LVDD but specific AUC or c-statistic values were not reported in the abstract.
  • The authors noted these findings should not be interpreted as establishing causal inference or diagnostic confirmation of OSA.
  • The model was characterized as supporting 'screening-oriented phenotypic characterization' rather than definitive diagnosis.

What This Means

This research suggests that among obese adults, those who screen as high-risk for obstructive sleep apnea (OSA) using a simple questionnaire called STOP-BANG are significantly more likely to have a heart condition called left ventricular diastolic dysfunction (LVDD), which is an early form of heart stiffness that can precede heart failure. In the study, 43% of obese participants had LVDD compared to only 7% of non-obese participants, and within the obese group, high OSA risk on the STOP-BANG questionnaire was associated with more than twice the odds of having LVDD even after accounting for other factors. The study also found that high-risk obese individuals tended to have more fat around the heart, higher levels of inflammatory markers in their blood, and worse autonomic nervous system function (measured through heart rate variability). The researchers proposed that a simple three-part screening model combining the STOP-BANG score, heart fat thickness measured by ultrasound, and blood inflammatory markers could help identify obese patients who are more likely to have LVDD. This is notable because all three components are relatively easy to measure in a clinical setting. The study was conducted at a single center with 279 participants (113 obese, 166 non-obese) and used standard echocardiographic criteria to diagnose LVDD. This research suggests that routine OSA risk screening in obese cardiac patients could help flag individuals who may need further cardiac evaluation for early heart dysfunction. However, the authors themselves caution that this cross-sectional study cannot prove that OSA causes LVDD, and the STOP-BANG questionnaire is a screening tool, not a diagnostic test for OSA. These findings point to a cluster of interconnected conditions — obesity, sleep apnea risk, heart fat, inflammation, and early heart dysfunction — that may warrant integrated screening approaches in clinical practice.

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Citation

Cosgun A, Oren H. (2026). STOP-BANG-Defined high OSA risk is associated with left ventricular diastolic dysfunction in obese adults.. Sleep &amp; breathing = Schlaf &amp; Atmung. https://doi.org/10.1007/s11325-026-03720-0