Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
1986-6-20
pubmed:abstractText
We previously reported the finding of phytosterolemia, xanthomatosis, and hyperapobetalipoproteinemia (hyperapoB) in five siblings in a large Amish pedigree ascertained through a 13-year-old boy who died suddenly from advanced coronary atherosclerosis. Here, we present further analyses of the plasma levels of the plant sterol, sitosterol, of low density (beta) lipoprotein (LDL) sterol, and of LDL B protein. Of 254 relatives and spouses of the proband, 90.5% were examined. A series of genetic models were explored using a pedigree analysis where parameters reflecting frequency, transmission, and penetrance of putative genotypes were examined simultaneously using a maximum likelihood approach. Segregation analysis of the sitosterol levels showed that the phenotype of sitosterolemia was controlled by a rare autosomal recessive gene. There was also significant familial correlation in plasma sitosterol levels that was attributed to a polygenic component under a mixed model but could also be due to shared environments such as diets. The recessive model was supported by our finding that the plasma sitosterol levels in the parents and in six children born to three of the five sitosterolemics were less than 1 mg/dl, well within the normal range. The phenotype of hyperapoB is based on an elevated level of LDL B protein in the presence of a normal LDL cholesterol level (low LDL sterol to LDL B ratio). For both LDL sterol and LDL B, a polygenic model showed a slightly greater improvement in ln likelihood than did the Mendelian single locus model when both were compared to a sporadic model. Similar results were obtained for sterol levels of high density (alpha) lipoprotein (HDL) sterol. When segregation analysis was performed using the ratio of LDL sterol to LDL B, the Mendelian single locus model gave a slightly better fit to the data than did the polygenic model. While the analyses presented here provided unequivocal evidence for the recessive phenotype of phytosterolemia, we also identified a possible single gene factor that could account for the major portion of the strong familial aggregation in the ratio of LDL sterol to LDL B, and to a lesser extent LDL B. However, there is clear evidence of familial aggregation for these traits in this pedigree beyond that due to Mendelian components.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/3706300-1246333, http://linkedlifedata.com/resource/pubmed/commentcorrection/3706300-172575, http://linkedlifedata.com/resource/pubmed/commentcorrection/3706300-3989379, http://linkedlifedata.com/resource/pubmed/commentcorrection/3706300-4360855, http://linkedlifedata.com/resource/pubmed/commentcorrection/3706300-4827918, http://linkedlifedata.com/resource/pubmed/commentcorrection/3706300-5441548, http://linkedlifedata.com/resource/pubmed/commentcorrection/3706300-6110091, http://linkedlifedata.com/resource/pubmed/commentcorrection/3706300-6333635, http://linkedlifedata.com/resource/pubmed/commentcorrection/3706300-6422918, http://linkedlifedata.com/resource/pubmed/commentcorrection/3706300-6768564, http://linkedlifedata.com/resource/pubmed/commentcorrection/3706300-6827984, http://linkedlifedata.com/resource/pubmed/commentcorrection/3706300-6928647, http://linkedlifedata.com/resource/pubmed/commentcorrection/3706300-7105675, http://linkedlifedata.com/resource/pubmed/commentcorrection/3706300-7149491, http://linkedlifedata.com/resource/pubmed/commentcorrection/3706300-946132, http://linkedlifedata.com/resource/pubmed/commentcorrection/3706300-993644
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
0002-9297
pubmed:author
pubmed:issnType
Print
pubmed:volume
38
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
492-504
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
1986
pubmed:articleTitle
Genetic analysis of plasma sitosterol, apoprotein B, and lipoproteins in a large Amish pedigree with sitosterolemia.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't