Key result
Lower high-frequency HRV is linked to ~10-fold higher NEC odds per SD in preterm infants.
Why the study?
Necrotizing enterocolitis is typically diagnosed only after becoming clinically significant, creating an urgent need for a non-invasive biomarker to detect patients at risk early.
Does the high frequency component of heart rate variability predict the risk of necrotizing enterocolitis in stable preterm infants?
Cohort (n=70)
Does the high frequency component of heart rate variability predict the risk of necrotizing enterocolitis in stable preterm infants?
Odds Ratio: 10
p-value: p=<0.001
Diminished vagal tone, measured by high-frequency heart rate variability, may serve as an early, non-invasive predictive biomarker for necrotizing enterocolitis in preterm infants.
May enable earlier NEC risk stratification in preterm infants; leaves open prospective validation before clinical adoption.
BACKGROUND: Necrotizing enterocolitis (NEC) is an acute neonatal inflammatory disease which may lead to intestinal necrosis, multisystem failure, and death. Currently, NEC is diagnosed by a combination of laboratory and radiographic tests conducted a posteriori i.e., when NEC is already clinically significant. Given the acute onset and rapid progression of NEC, a non-invasive biomarker that allows early detection of patients at risk is required as a matter of urgency. We evaluated whether the high frequency (HF) component of heart rate variability (HRV), a measure of vagal efferent tonic cholinergic activity may be used as a predictive biomarker for NEC-risk before the onset of clinical disease. METHODS: In this prospective study, stable preterm (gestational age 28-35 weeks) infants had HRV power spectra analyzed from surface electrocardiogram waveforms taken at rest on day 5-8 of life. We used regression modeling to determine the utility of HF-HRV in predicting NEC. KEY RESULTS: HF-HRV power was 21.5 ± 2.7 and 3.9 ± 0.81 ms(2) in infants that remained healthy and those that later developed stage 2+ NEC, respectively (p < 0.001). Nine of 70 enrolled infants developed NEC. The ROC discriminated a HF-HRV value of 4.68 ms(2) predictive for developing NEC with a sensitivity and specificity of 89% and 87%, and positive and negative predictive value of 50% and 98%, respectively. With predictive regression modeling, the risk (odds ratio) of developing NEC was 10 per every one SD decrease in HF-HRV. CONCLUSIONS & INFERENCES: Our preliminary data indicate that HF-HRV may serve as a potential, non-invasive predictive biomarker of NEC-risk in NICU infants.
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Doheny et al. (2014) conducted a cohort in Necrotizing enterocolitis (n=70). Decreased high frequency heart rate variability (HF-HRV) vs. Higher HF-HRV was evaluated on Development of stage 2+ necrotizing enterocolitis (OR 10, p=<0.001). A one standard deviation decrease in high frequency heart rate variability was associated with a 10-fold increased odds of developing necrotizing enterocolitis in preterm infants.
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