Evidence map›Paper›PMID 20920215›Full record

GuidelineOrphanet journal of rare diseases2010

Guidelines for the diagnosis and management of chylomicron retention disease based on a review of the literature and the experience of two centers.

Noel Peretti, Agnès Sassolas, Claude C Roy, Colette Deslandres, Mathilde Charcosset, Justine Castagnetti, Laurence Pugnet-Chardon, Philippe Moulin, Sylvie Labarge, Lise Bouthillier and 4 more

Open access · goldAbstract readPractice GuidelineReview
In one paragraph

Guideline in Orphanet journal of rare diseases, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
9.2field-weighted citation impact, top 2% of its field
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

33 citing papers in PubMed, 143 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Exploring Plasma Coenzyme QAntioxidants (Basel, Switzerland) · 2024
    Article
  5. Review
  6. Current Diagnosis and Management of Familial Hypobetalipoproteinemia 1.Journal of atherosclerosis and thrombosis · 2024
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Current Diagnosis and Management of Abetalipoproteinemia.Journal of atherosclerosis and thrombosis · 2021
    Review
  12. Review
  13. Review
  14. Article
  15. Review
  16. Neurology of Nutritional Deficiencies.Current neurology and neuroscience reports · 2019
    Review
  17. Article
  18. Article
  19. Chylomicron Retention Disease: a Description of a New Mutation in a Very Rare Disease.Pediatric gastroenterology, hepatology & nutrition · 2018
    Article
  20. Low levels of very-long-chainJournal of nutritional science · 2017
    Article
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 at 6 institutions in 2 countries.

Noel PerettiDepartment of Nutrition, CHU Sainte-Justine Research Center, Université de Montréal, 3175, Ste-Catherine Road, Montreal, Quebec, H3T 1C5, Canada.
Agnès Sassolas
Claude C Roy
Colette Deslandres
Mathilde Charcosset
Justine Castagnetti
Laurence Pugnet-Chardon
Philippe Moulin
Sylvie Labarge
Lise Bouthillier
Alain Lachaux
Emile Levy
Department of Nutrition-Hepatogastroenterology, Hôpital Femme Mère Enfant, Bron, Université Lyon 1
Department of Pediatrics, CHU Sainte-Justine Research Center, Université de Montréal
Centre Hospitalier Universitaire Sainte-Justine · CAHôpital Femme Mère Enfant · FRInserm · FRUniversité Claude Bernard Lyon 1 · FRUniversité de Montréal · CAHospices Civils de Lyon · FR

Funding

Canadian Institutes of Health Research MOP 10584
6 · The paper itself

Abstract

Familial hypocholesterolemia, namely abetalipoproteinemia, hypobetalipoproteinemia and chylomicron retention disease (CRD), are rare genetic diseases that cause malnutrition, failure to thrive, growth failure and vitamin E deficiency, as well as other complications. Recently, the gene implicated in CRD was identified. The diagnosis is often delayed because symptoms are nonspecific. Treatment and follow-up remain poorly defined.The aim of this paper is to provide guidelines for the diagnosis, treatment and follow-up of children with CRD based on a literature overview and two pediatric centers 'experience.The diagnosis is based on a history of chronic diarrhea with fat malabsorption and abnormal lipid profile. Upper endoscopy and histology reveal fat-laden enterocytes whereas vitamin E deficiency is invariably present. Creatine kinase (CK) is usually elevated and hepatic steatosis is common. Genotyping identifies the Sar1b gene mutation.Treatment should be aimed at preventing potential complications. Vomiting, diarrhea and abdominal distension improve on a low-long chain fat diet. Failure to thrive is one of the most common initial clinical findings. Neurological and ophthalmologic complications in CRD are less severe than in other types of familial hypocholesterolemia. However, the vitamin E deficiency status plays a pivotal role in preventing neurological complications. Essential fatty acid (EFA) deficiency is especially severe early in life. Recently, increased CK levels and cardiomyopathy have been described in addition to muscular manifestations. Poor mineralization and delayed bone maturation do occur. A moderate degree of macrovesicular steatosis is common, but no cases of steatohepatitis cirrhosis. Besides a low-long chain fat diet made up uniquely of polyunsaturated fatty acids, treatment includes fat-soluble vitamin supplements and large amounts of vitamin E. Despite fat malabsorption and the absence of postprandial chylomicrons, the oral route can prevent neurological complications even though serum levels of vitamin E remain chronically low. Dietary counseling is needed not only to monitor fat intake and improve symptoms, but also to maintain sufficient caloric and EFA intake. Despite a better understanding of the pathogenesis of CRD, the diagnosis and management of the disease remain a challenge for clinicians. The clinical guidelines proposed will helpfully lead to an earlier diagnosis and the prevention of complications.

Indexed as

AdultAnthropometryChildChild, PreschoolChylomicronsCohort StudiesDiarrheaFatty AcidsFemaleGrowth DisordersHumansInfantLipid Metabolism DisordersMalabsorption SyndromesMaleMalnutritionChylomicronsFatty AcidsMonomeric GTP-Binding ProteinsSAR1B protein, human

Identifiers

PMID20920215
PMCPMC2956717
OpenAlexW2141636439

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.