Evidence map›Paper›PMID 42368277›Full record

ArticleFrontiers in pediatrics2026

Triglyceride profiles in preterm infants reveal dynamic and age-specific trajectories.

Emma R Gertel, Victoria Y Ding, Thanaphong Phongpreecha, Feng Xie, Andrew Parsons, Ivana Marić, Nima Aghaeepour, Karl G Sylvester, Valerie Y Chock, John A Kerner and 4 more

Abstract read
In one paragraph

Article in Frontiers in pediatrics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Emma R GertelSackler School of Medicine, American Medical Program, Tel Aviv University, Tel Aviv, Israel.
Victoria Y DingStanford Quantitative Sciences Unit, Palo Alto, CA, United States.
Thanaphong PhongpreechaDepartment of Anesthesiology, Pain and Perioperative Medicine, Stanford University, Stanford, CA, United States.
Feng XieDivision of Computational Health Sciences, Department of Surgery, University of Minnesota, Minneapolis, MN, United States.
Andrew ParsonsDepartment of Pediatrics, Division of Neonatology, Stanford University, Stanford, CA, United States.
Ivana MarićDepartment of Pediatrics, Division of Neonatology, Stanford University, Stanford, CA, United States.
Nima AghaeepourDepartment of Anesthesiology, Pain and Perioperative Medicine, Stanford University, Stanford, CA, United States.
Karl G SylvesterStanford Department of Surgery, Division of Pediatric Surgery, Stanford University, Palo Alto, CA, United States.
Valerie Y ChockDepartment of Pediatrics, Division of Neonatology, Stanford University, Stanford, CA, United States.
John A KernerStanford Department of Pediatrics, Division of Gastroenterology, Stanford University, Palo Alto, CA, United States.
Camilia R MartinDepartment of Pediatrics, Division of Neonatology, Weill Cornell Medicine, New York, NY, United States.
David K StevensonDepartment of Pediatrics, Division of Neonatology, Stanford University, Stanford, CA, United States.
Gary M ShawDepartment of Pediatrics, Division of Neonatology, Stanford University, Stanford, CA, United States.
Jonathan D ReissDepartment of Pediatrics, Division of Neonatology, Stanford University, Stanford, CA, United States.

Funding

An Investigation of Omics for Bronchopulmonary DypslasiaK23HL173645 · NHLBI · STANFORD UNIVERSITY · PI JONATHAN REISS · 2025 to 2026
$385k
NHLBI NIH HHS K23 HL173645
6 · The paper itself

Abstract

Introduction: Triglyceride (TG) values are routinely monitored in preterm infants receiving lipid emulsion therapy, but their clinical utility remains poorly defined. The objective of this study was to define TG values and their associations with gestational age (GA), birth weight (BW), lipid dosing and postnatal age in preterm infants born <32 weeks' across two distinct academic medical centers. Methods: We conducted a retrospective multi-centered observational study using data from the Lucile Packard Children's Hospital (LPCH) Stanford Neonatal Intensive Care Unit and the Beth Israel Deaconess Medical Center (BIDMC) Neonatal Intensive Care Unit. TG values in infants <32 weeks' GA were interrogated by GA, postnatal age, BW and in aggregate. Pre- and postnatal factors were evaluated using multivariable logistic regression in the LPCH Stanford data set for associations with hypertriglyceridemia, defined using thresholds of 200 mg/dL and 250 mg/dL. Spline regression was used to model the relationship between continuous TG values and postnatal outcomes in both data sets. Results: TG distributions differed significantly by GA, with the highest values observed among infants born at 22-25 weeks' gestation and/or with extremely low birth weight. In the LPCH 22-25 week cohort, TG levels peaked at approximately two weeks of postnatal age and subsequently declined. Lipid emulsion dosing <2 g/kg/day was associated with a reduced risk of hypertriglyceridemia, whereas dosing >2 g/kg/day did not significantly alter risk. Continuous TG values were not consistently associated with major neonatal outcomes, including respiratory distress syndrome (RDS), bronchopulmonary dysplasia (BPD), necrotizing enterocolitis (NEC), or retinopathy of prematurity (ROP) in either cohort. Discussion: TG values in preterm infants vary by developmental stage, closely reflecting GA, BW, and postnatal age, suggesting that circulating TG levels are developmentally regulated. These findings support consideration of age- or weight-based TG reference ranges, particularly for infants born at 22-25 weeks' gestation. In contrast, the limited association between TG levels and neonatal morbidities raises questions regarding the relevance of early TG measurements for predicting later disease.

Indexed as

birth weightgestational agelipidsNICUpreterm infantstriglycerides

Identifiers

PMID42368277
PMCPMC13303854

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.