Evidence map›Paper›PMID 40722188›Full record

ArticleOrphanet journal of rare diseases2025

Use of cholic acid in Smith-Lemli-Opitz syndrome (SLOS): real-world patient outcomes.

Edwin Ferren, Paul R Hillman, Amy Kritzer, Joseph Ray, Alvaro Serrano, Hope Northrup, Paige Roberts, Rana Dutta, Tiziano Pramparo, Pamela Vig and 1 more

Abstract read
In one paragraph

Article in Orphanet journal of rare diseases, 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

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

11 authors.

Edwin FerrenDepartment of Genetics, Atrium Health Levine Children's Hospital, 1001 Blythe Blvd, Charlotte, NC, USA. Edwin.Ferren@atriumhealth.org.
Paul R HillmanDepartment of Pediatrics, Division of Medical Genetics, McGovern Medical School at UTHealth Houston, Houston, TX, USA.
Amy KritzerBoston Children's Hospital, Boston, MA, USA.
Joseph RayUniversity of Texas Medical Branch, Houston, TX, USA.
Alvaro SerranoEast Tennessee State University, Johnson City, TN, USA.
Hope NorthrupDepartment of Pediatrics, Division of Medical Genetics, McGovern Medical School at UTHealth Houston, Houston, TX, USA.
Paige RobertsDepartment of Pediatrics, Division of Medical Genetics, McGovern Medical School at UTHealth Houston, Houston, TX, USA.
Rana DuttaMirum Pharmaceuticals, Inc., Foster City, CA, USA.
Tiziano PramparoMirum Pharmaceuticals, Inc., Foster City, CA, USA.
Pamela VigMirum Pharmaceuticals, Inc., Foster City, CA, USA.
Robert D SteinerUniversity of Wisconsin School of Medicine and Public Health, Madison, WI, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSmith-Lemli-Opitz Syndrome (SLOS) is an autosomal recessive disorder of cholesterol biosynthesis caused by biallelic pathogenic variants in DHCR7, which encodes the enzyme 7-dehydrocholesterol reductase (DHCR7). SLOS is a multisystemic disorder affecting various aspects of health, including growth, development, behavior, and quality of life, underscoring the need for safe, efficacious interventions that limit disease burden. DHCR7 enzyme deficiency leads to a "metabolic block" resulting in decreased cholesterol production and accumulation of its precursor 7-dehydrocholesterol and the secondary isomer 8-dehydrocholesterol. Reduced cholesterol synthesis, in turn, leads to decreased levels of cholic acid (CA), an endogenous bile acid synthesized from cholesterol and essential for cholesterol absorption. Dietary cholesterol supplementation is standard therapy. Bile acid supplementation with CA has been shown to improve dietary cholesterol absorption and raise plasma cholesterol levels. However, there is a paucity of patient-level data regarding the utility of CA as a treatment for SLOS. The purpose of this case series is to address the lack of comprehensive patient data through documentation of the outcomes of a company-sponsored CA patient experience program. A retrospective chart review was conducted for these individuals while on CA plus cholesterol supplementation. Data for demographics and key clinical/laboratory parameters were captured with a standardized data collection tool.

resultsEight genetically confirmed individuals with SLOS (age range 1 to 20 years) with median plasma cholesterol levels at baseline ≤ 125 mg/dL were treated with CA at 10-15 mg/kg/d for 30 to 450 days. Exogenous CA administration improved cholesterol levels in the majority of patients. Growth improved after CA initiation and trended toward age-appropriate growth percentiles. Reports from the patient, parent/caregiver, and/or healthcare professional noted positive behavioral changes leading to increased social interaction, cognitive engagement, and improved communication skills. Improvements in biochemical parameters and quality of life were also observed in several patients after CA treatment. CA supplementation was well tolerated with minimal adverse events.

conclusionsThe cumulative experiences of eight patients provide a compelling narrative supporting the potential utility of CA treatment in SLOS while underscoring the safety of CA in this patient population. Larger longitudinal studies of CA in patients with SLOS are warranted.

Indexed as

Cholic AcidSmith-Lemli-Opitz SyndromeAdolescentChildChild, PreschoolCholesterolFemaleHumansInfantMaleOxidoreductases Acting on CH-CH Group DonorsYoung Adult7-dehydrocholesterol reductaseCholesterolCholic AcidOxidoreductases Acting on CH-CH Group Donors7-dehydrocholesterol7-dehydrocholesterol reductase (DHCR7)7-DHC8-dehydrocholesterol8-DHCCholesterolCholesterol deficiencyCholic acidRSH syndromeSLOSSmith-Lemli-Opitz syndrome

Identifiers

PMID40722188
PMCPMC12306108

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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.