Evidence map›Paper›PMID 41126187›Full record

Observational studyLipids in health and disease2025

Use of a cholesterol emulsion in Smith-Lemli-Opitz syndrome (SLOS): A single-center observational study, retrospective analysis and structured caregiver interview.

Tobias Fischer, Alicia Born, Simone Harmeling, Manfred Fobker, Ulrike Och, Christiane Elpers, Thorsten Marquardt

Abstract readObservational Study
In one paragraph

Observational study in Lipids in health and disease, 2025. 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

7 authors.

Tobias Fischer *Center for Nutrition and Therapy (NuT), University of Applied Sciences Muenster, Corrensstraße 25, 48149, Muenster, Germany. tobias.fischer@fh-muenster.de.
Alicia Born *Center for Nutrition and Therapy (NuT), University of Applied Sciences Muenster, Corrensstraße 25, 48149, Muenster, Germany.
Simone HarmelingDepartment of Pediatrics, University Hospital Muenster, Albert-Schweitzer-Campus 1, 48149, Muenster, Germany.
Manfred FobkerCentral Laboratory, University Hospital Muenster, Albert-Schweitzer-Campus 1, 48149, Muenster, Germany.
Ulrike OchDepartment of Pediatrics, University Hospital Muenster, Albert-Schweitzer-Campus 1, 48149, Muenster, Germany.
Christiane ElpersChristian children's hospital (CKO), Johannisfreiheit 1, 49074, Osnabrück, Germany.
Thorsten MarquardtDepartment of Pediatrics, University Hospital Muenster, Albert-Schweitzer-Campus 1, 48149, Muenster, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSmith-Lemli-Opitz syndrome (SLOS) is a rare autosomal recessive disorder of cholesterol biosynthesis. SLOS leads to increased levels of 7-dehydrocholesterol (7-DHC) and decreased levels of total cholesterol (TC). Dietary therapy usually involves supplementation with cholesterol in an oil-based or, less commonly, an aqueous cholesterol suspension. The limited solubility of cholesterol can result in uneven distribution, sedimentation and clumping.

methodsIn seven patients (6 m, 1 f, 1-12 years) the previously administered dose of cholesterol was replaced by a newly developed emulsion and primary parameters TC, 7-DHC, HDL, LDL, vitamin D (25; 1-25), height and weight were determined. In addition, a personal structured interview was conducted with the caregivers of five participants to determine their satisfaction with the product, the care, and the effects on behaviour and health.

resultsOne patient was excluded due to non-compliance (N = 6). Before the intervention, the mean TC level was 42 ± 9 mg/dl (min = 29, max = 52; n = 5) and increased by at least 95% and at most 299% (163 ± 93%). 7-DHC levels showed a decrease of -28% to -96% (-63 ± 29%). No effect on anthropometric parameters was observed. Overall, the families were satisfied with the care and the effect of the emulsion was predominantly described as successful. The emulsion and its application were well tolerated with few side effects.

conclusionsOverall, there was an improved effect on TC and 7-DHC levels compared to standard therapy, with high patient satisfaction and low side effects.

Indexed as

CholesterolSmith-Lemli-Opitz SyndromeCaregiversChildChild, PreschoolCholesterol, HDLDehydrocholesterolsEmulsionsFemaleHumansInfantMaleRetrospective StudiesVitamin D7-dehydrocholesterolCholesterolCholesterol, HDLDehydrocholesterolsEmulsionsVitamin DCholesterolCholesterol emulsionCholesterol metabolism deficiencyCholesterol supplementationCongenital metabolic diseasesDietary supplementDietetic therapyMetabolic diseasesSLOSLOSSmith-Lemli-Opitz syndrome

Identifiers

PMID41126187
PMCPMC12541952

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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.