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PMID: 16029460 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Stomatocytic haemolysis and macrothrombocytopenia (Mediterranean stomatocytosis/macrothrombocytopenia) is the haematological presentation of phytosterolaemia.

British journal of haematology ·Vol. 130 ·No. 2 ·2005-07-00 ·Pages 297-309

Rees DC, Iolascon A, Carella M, O'marcaigh AS, Kendra JR, Jowitt SN, Wales JK, Vora A, Makris M, Manning N, Nicolaou A, Fisher J, Mann A, Machin SJ, Clayton PT, Gasparini P, Stewart GW

Abstract

Phytosterolaemia (sitosterolaemia) is a recessively inherited metabolic condition in which the absorption of both cholesterol and plant-derived cholesterol-like molecules at the gut is unselective and unrestricted. In haematology, Mediterranean stomatocytosis or Mediterranean macrothrombocytopenia is a poorly understood haematological condition that combines stomatocytic haemolysis with the presence of very large platelets. Five pedigrees showing this haematology were identified. Gas chromatography mass spectrometry (GC-MS) showed that all of the patients with this highly specific haematology had grossly elevated levels of phytosterols in the blood, diagnostic of phytosterolaemia. All showed mutations in the ABCG5 and ABCG8 previously linked to phytosterolaemia. Three pedigrees showed five new mutations, while two pedigrees showed the common W361X mutation in ABCG8. We draw the following four conclusions: (i) that Mediterranean stomatocytosis/macrothrombocytopenia is caused by an excess of phytosterols in the blood; (ii) that phytosterolaemia, which does not respond to standard statin treatment, can be diagnosed via the distinctive haematology described here, even when the cholesterol is normal; (iii) that phytosterolaemia should be considered in the differential diagnosis of all patients with large platelets; and (iv) that the platelet size should be noted in patients with hypercholesterolaemia.

MeSH Terms
ATP Binding Cassette Transporter, Subfamily G, Member 5 ATP Binding Cassette Transporter, Subfamily G, Member 8 ATP-Binding Cassette Transporters/genetics Adolescent Adult Blood Platelets/physiology,ultrastructure Child Erythrocyte Membrane/chemistry Erythrocytes, Abnormal/pathology Female Hemolysis Humans Lipoproteins/genetics Magnetic Resonance Spectroscopy Male Mutation Pedigree Phytosterols/blood Steroid Metabolism, Inborn Errors/blood,complications,genetics Thrombocytopenia/blood,etiology,genetics
Chemicals
ABCG5 protein, human ABCG8 protein, human ATP Binding Cassette Transporter, Subfamily G, Member 5 ATP Binding Cassette Transporter, Subfamily G, Member 8 ATP-Binding Cassette Transporters Lipoproteins Phytosterols
Authors & Affiliations
17 authors, click to expand affiliations / ORCID
Rees David C
Sheffield Children's Hospital, Royal Hallamshire Hospital, Sheffield, UK.
Iolascon Achille
Carella Massimo
O'marcaigh Aengus S
Kendra James R
Jowitt Simon N
Wales J K
Vora Ajay
Makris M
Manning Nigel
Nicolaou Anna
Fisher Julie
Mann Anuska
Machin Samuel J
Clayton Peter T
Gasparini Paolo
Stewart Gordon W
Article Info
Journal
British journal of haematology
Abbr.
Br J Haematol
ISSN
0007-1048
Published
2005-07-00
Pages
297-309
Language
English
Region
England
NLM ID
0372544
Subset
IM
Grants
Telethon · GGP02202 · Italy
Wellcome Trust · United Kingdom
Corrections
CommentIn
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