<?xml version="1.0" encoding="UTF-8"?><rss version="2.0"
	xmlns:content="http://purl.org/rss/1.0/modules/content/"
	xmlns:wfw="http://wellformedweb.org/CommentAPI/"
	xmlns:dc="http://purl.org/dc/elements/1.1/"
	xmlns:atom="http://www.w3.org/2005/Atom"
	xmlns:sy="http://purl.org/rss/1.0/modules/syndication/"
	xmlns:slash="http://purl.org/rss/1.0/modules/slash/"
	>

<channel>
	<title>association between L-carnitine and ROP &#8211; Science</title>
	<atom:link href="https://scienmag.com/tag/association-between-l-carnitine-and-rop/feed/" rel="self" type="application/rss+xml" />
	<link>https://scienmag.com</link>
	<description></description>
	<lastBuildDate>Tue, 20 Oct 2026 10:49:29 +0000</lastBuildDate>
	<language>en-US</language>
	<sy:updatePeriod>
	hourly	</sy:updatePeriod>
	<sy:updateFrequency>
	1	</sy:updateFrequency>
	<generator>https://wordpress.org/?v=7.1.3</generator>

<image>
	<url>https://scienmag.com/wp-content/uploads/2024/07/cropped-scienmag_ico-32x32.jpg</url>
	<title>association between L-carnitine and ROP &#8211; Science</title>
	<link>https://scienmag.com</link>
	<width>32</width>
	<height>32</height>
</image> 
<site xmlns="com-wordpress:feed-additions:1">73899611</site>	<item>
		<title>Retrospective cohort links early L-carnitine to lower ROP incidence in preterm infants</title>
		<link>https://scienmag.com/retrospective-cohort-links-early-l-carnitine-to-lower-rop-incidence-in-preterm-infants/</link>
		
		<dc:creator><![CDATA[Harold Sullivan]]></dc:creator>
		<pubDate>Tue, 20 Oct 2026 10:49:29 +0000</pubDate>
				<category><![CDATA[Medicine]]></category>
		<category><![CDATA[association between L-carnitine and ROP]]></category>
		<category><![CDATA[birth weight]]></category>
		<category><![CDATA[early]]></category>
		<category><![CDATA[early L-carnitine supplementation]]></category>
		<category><![CDATA[Effect]]></category>
		<category><![CDATA[fatty acid oxidation]]></category>
		<category><![CDATA[gestational age]]></category>
		<category><![CDATA[L-carnitine]]></category>
		<category><![CDATA[lower retinopathy of prematurity incidence]]></category>
		<category><![CDATA[neonatal eye disease]]></category>
		<category><![CDATA[neonatal ophthalmology]]></category>
		<category><![CDATA[neonatal supplementation benefits]]></category>
		<category><![CDATA[observational study]]></category>
		<category><![CDATA[observational study on neonatal outcomes]]></category>
		<category><![CDATA[ophthalmic disease prevention in preemies]]></category>
		<category><![CDATA[preterm infant health interventions]]></category>
		<category><![CDATA[preterm infants]]></category>
		<category><![CDATA[retinopathy of prematurity]]></category>
		<category><![CDATA[retrospective cohort]]></category>
		<category><![CDATA[retrospective cohort study]]></category>
		<category><![CDATA[ROP screening outcomes]]></category>
		<category><![CDATA[Type 2 ROP]]></category>
		<category><![CDATA[Type 2 ROP reduction]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=318030</guid>

					<description><![CDATA[A retrospective cohort of 267 preterm infants associated early prophylactic L-carnitine supplementation with lower overall and Type 2 retinopathy of prematurity, but not Type 1 ROP, without establishing causality.]]></description>
										<content:encoded><![CDATA[<p>In a retrospective cohort study of 267 preterm infants who met screening criteria for retinopathy of prematurity, early prophylactic L-carnitine supplementation was associated with lower incidence of the blinding eye disease overall and of Type 2 ROP. Researchers reported that ROP occurred in 17.5% of the 63 infants in the L-carnitine-exposed group, compared with 38.2% of the 204 infants in the non-exposed control group, a difference reported as statistically significant at P = 0.002. Type 2 ROP occurred in 6.3% and 20.6% of the respective groups, with P = 0.009.</p>
<p>The study detected no significant between-group difference in Type 1 ROP. Because the investigation was observational, the results establish an association rather than demonstrating that L-carnitine supplementation caused the lower incidence. The study examined whether exposure to L-carnitine during the neonatal period was associated with outcomes among preterm infants eligible for ROP screening.</p>
<p>The exposed group comprised 63 infants and the control group 204 infants. Investigators collected baseline demographic information, clinical-treatment data and outcome data, and designated overall ROP incidence, Type 1 ROP and Type 2 ROP as the primary outcomes. They also compared secondary neonatal complications.</p>
<p>Baseline characteristics were comparable between the groups in the reported statistical tests, with all P values above 0.05. Subgroup and interaction analyses were stratified by sex, gestational age and birth weight, while multivariate logistic regression assessed factors associated with Type 2 ROP. Beyond the lower incidence of overall and Type 2 ROP, the L-carnitine-exposed group had a lower blood-transfusion rate than the control group: 49.2% versus 66.2%, with P = 0.015.</p>
<p>No significant differences were detected between the groups for Type 1 ROP, sepsis, bronchopulmonary dysplasia, necrotizing enterocolitis, intraventricular hemorrhage or periventricular leukomalacia; all corresponding P values were above 0.05. Multivariate logistic regression found that early L-carnitine supplementation was independently associated with lower odds of Type 2 ROP, with an odds ratio of 0.253, a 95% confidence interval of 0.085–0.756 and P = 0.014. The reported analysis therefore identifies an association that persisted after adjustment for the factors entered into the model, but it does not remove the potential influence of unmeasured differences between infants or treatment decisions.</p>
<p>Interaction tests indicated that the association between L-carnitine exposure and ROP varied according to gestational age and birth weight, with both interaction P values below 0.05. The potentially stronger association was observed among infants born at 30–32 weeks’ gestation and weighing at least 1,500 grams. No significant interaction with infant sex was found, with P above 0.05.</p>
<p>These analyses do not establish that L-carnitine is specifically protective for the subgroup with the stronger observed association; rather, they show that the relationship differed according to these infant characteristics in the available data. The proposed biological rationale centers on energy metabolism and oxidative stress, both described in the study as key mechanisms in ROP. The findings are also limited to the studied population of preterm infants who met ROP screening criteria, and the group receiving supplementation was smaller than the control group.</p>
<p>The authors concluded that the results support an association between early prophylactic L-carnitine supplementation and reduced risks of overall and Type 2 ROP, with no detectable association for Type 1 ROP. They called for large-scale prospective randomized controlled trials to determine whether the supplement produces a genuine protective effect; the present findings alone cannot establish efficacy or causality.</p>
<p><strong>Subject of Research:</strong> Association between early prophylactic L-carnitine supplementation and retinopathy of prematurity in preterm infants</p>
<p><strong>Article Title:</strong> The effect of early prophylactic L-carnitine supplementation on retinopathy of prematurity: a retrospective cohort study</p>
<p><strong>Article References:</strong> Bai, S., Sun, Z., Li, M., Yu, Z., Shi, C., Xu, F., &amp; Sun, H. (2026). The effect of early prophylactic L-carnitine supplementation on retinopathy of prematurity: a retrospective cohort study. <em>BMC Pediatrics</em>. <a href="https://doi.org/10.1186/s12887-026-07770-x" rel="noopener noreferrer">https://doi.org/10.1186/s12887-026-07770-x</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1186/s12887-026-07770-x" rel="noopener noreferrer">10.1186/s12887-026-07770-x</a></p>
<p><strong>Keywords:</strong> L-carnitine, retinopathy of prematurity, preterm infants, neonatal eye disease, retrospective cohort, Type 2 ROP, fatty acid oxidation, gestational age, birth weight, observational study, effect, early</p>
]]></content:encoded>
					
		
		
		<post-id xmlns="com-wordpress:feed-additions:1">318030</post-id>	</item>
	</channel>
</rss>
