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Record W2588407548 · doi:10.1161/atvb.32.suppl_1.a134

Abstract 134: A Double Heterozygote for LCAT and ABCA1 Mutations Accounts for Severe Hypoalphalipoproteinemia

2012· article· en· W2588407548 on OpenAlexaff
Adam D. McIntyre, Robert A. Hegele

Bibliographic record

VenueArteriosclerosis Thrombosis and Vascular Biology · 2012
Typearticle
Languageen
FieldMedicine
TopicCholesterol and Lipid Metabolism
Canadian institutionsWestern University
Fundersnot available
KeywordsProbandTangier diseaseCompound heterozygosityGeneticsHeterozygote advantageAsymptomaticLocus (genetics)BrotherEndocrinologyFamilial hypercholesterolemiaMedicineInternal medicineMutationABCA1GeneCholesterolAlleleBiology

Abstract

fetched live from OpenAlex

We report a family with extremely depressed high density lipoprotein (HDL) cholesterol (C) levels. The proband, a 27 year-old male of Asian Indian origin, was identified on routine lipid screening to have an HDL-C of 9mg/dL. His 24 year-old brother had an HDL-C of 6mg/dL and was therefore referred to a local lipid clinic in 1997. Both brothers were asymptomatic. The nuclear family was comprised of another brother and a mother living in India; their father had died previously from an undetermined cause. The parents were second cousins. Blood was obtained from members of the extended family and showed that the mother’s HDL-C was reduced at 29mg/dL, while the 3rd bother had a normal HDL-C at 54mg/dL. Based on the above scenario, a homozygous mutation most likely involving ABCA1 was presumed to be responsible for this lipoprotein profile. However, microsatellite marker analyses of the ABCA1 locus showed no homozygosity pattern in the two affected brothers. Further analyses of the APOA1-C3-A4 locus similarly failed to show homozygosity in the affected brothers. Plasma activities of both salt-stimulated paraoxanase and LCAT were at the low end of normal. Direct sequence analyses of the LCAT gene showed all three brothers were heterozygous for the Arg423His mutation, while the mother’s LCAT gene sequence was normal. No further work was pursued until 2011, when this family’s DNA was re-examined by direct sequencing. On this occasion, a heterozygous mutation in ABCA1 was found, namely Arg1270X in the 2 affected brothers and their mother. To our knowledge, this is the first report of ’double heterozygosity’ for LCAT and ABCA1 mutations producing severe hypoalphalipoproteinemia. Further, simple heterozygosity for the ABCA1 Arg1270X mutation had a co-dominant influence, moderately reducing HDL-C levels. In contrast, simple heterozygosity for the LCAT Arg423His mutation had no effect on HDL-C, but in the presence of ABCA1 Arg1270X it contributed to markedly reduced HDL-C. This case report highlights a potential pitfall in human genetic studies, namely assuming a particular inheritance pattern based upon family structure. It also highlights the value of perseverance by searching for causative mutations in more than one gene.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.001
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Case report · Consensus signal: Case report
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.007
Threshold uncertainty score0.024

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.001
Meta-epidemiology (narrow)0.0030.001
Meta-epidemiology (broad)0.0010.001
Bibliometrics0.0010.001
Science and technology studies0.0010.001
Scholarly communication0.0010.000
Open science0.0010.001
Research integrity0.0020.001
Insufficient payload (model declined to judge)0.0070.002

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.065
GPT teacher head0.332
Teacher spread0.267 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designCase report
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations0
Published2012
Admission routes1
Has abstractyes

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