Literature DB >> 17627709

Ageing in Marfan syndrome.

A Hasan1, J Poloniecki, A Child.   

Abstract

AIMS: Marfan syndrome (MFS) is a dominantly inherited connective tissue disorder caused by mutations in the fibrillin-1 gene. Past research has focused on younger patients as lifespan was known to be significantly reduced. This study aims to describe the complications, including those affecting the eyes, heart and musculoskeletal system, faced by older survivors.
METHODS: All 2500 patient records from the National Marfan Syndrome Clinical Database were searched for suitable participants aged 50 or older. One hundred and fifty-six questionnaires were posted to patients with MFS. These patients were sent a detailed questionnaire regarding medical aspects of their disease. Those included in the study were sent questionnaires for spouses and friends (not blood relatives) to complete, to provide control data. Other age- and sex-matched controls were recruited locally.
RESULTS: Sixty questionnaires from patients with MFS (35%) were returned and eligible for inclusion in the study, comprising 28 female patients and 32 male patients with a median age of 57. We recruited 56 eligible controls. Our results revealed that patients over 50 years of age with MFS may be at a higher risk than previously assumed for retinal detachment (reported by 24% of our respondents) and cardiovascular abnormalities (42% have had past aortic surgery; 53% report palpitation). Lesser known complications were also reported, including cataract (reported by 27%).
CONCLUSIONS: Medical practitioners should be aware of the range of complications that can occur in patients with MFS in addition to the normal ageing process. Health problems in MFS patients over 50 may require investigation and specific therapy earlier than in the normal ageing population, because of the degenerative nature of this genetic condition.

Entities:  

Mesh:

Year:  2007        PMID: 17627709     DOI: 10.1111/j.1742-1241.2007.01407.x

Source DB:  PubMed          Journal:  Int J Clin Pract        ISSN: 1368-5031            Impact factor:   2.503


  7 in total

Review 1.  Non-cardiac manifestations of Marfan syndrome.

Authors:  Anne H Child
Journal:  Ann Cardiothorac Surg       Date:  2017-11

2.  Characterization of pain, disability, and psychological burden in Marfan syndrome.

Authors:  Traci J Speed; Vani A Mathur; Matthew Hand; Bryt Christensen; Paul D Sponseller; Kayode A Williams; Claudia M Campbell
Journal:  Am J Med Genet A       Date:  2016-11-14       Impact factor: 2.802

3.  Prevalence data on all Ghent features in a cross-sectional study of 87 adults with proven Marfan syndrome.

Authors:  Svend Rand-Hendriksen; Rigmor Lundby; Lena Tjeldhorn; Kai Andersen; Jon Offstad; Svein Ove Semb; Hans-Jørgen Smith; Benedicte Paus; Odd Geiran
Journal:  Eur J Hum Genet       Date:  2009-03-18       Impact factor: 4.246

Review 4.  Joint hypermobility as a distinctive feature in the differential diagnosis of myopathies.

Authors:  N C Voermans; C G Bonnemann; B C J Hamel; H Jungbluth; B G van Engelen
Journal:  J Neurol       Date:  2009-02-09       Impact factor: 4.849

5.  Identification of a novel FBN1 gene mutation in a large Pakistani family with Marfan syndrome.

Authors:  Shazia Micheal; Muhammad Imran Khan; Farah Akhtar; Marjan M Weiss; Farah Islam; Mehmood Ali; Raheel Qamar; Alessandra Maugeri; Anneke I den Hollander
Journal:  Mol Vis       Date:  2012-07-18       Impact factor: 2.367

Review 6.  The Musculoskeletal Manifestations of Marfan Syndrome: Diagnosis, Impact, and Management.

Authors:  Lily Pollock; Ashley Ridout; James Teh; Colin Nnadi; Dionisios Stavroulias; Alex Pitcher; Edward Blair; Paul Wordsworth; Tonia L Vincent
Journal:  Curr Rheumatol Rep       Date:  2021-11-26       Impact factor: 4.592

7.  Informative STR Markers for Marfan Syndrome in Birjand, Iran.

Authors:  Ezzat Dadkhah; Masood Ziaee; Mohammad Hossein Davari; Toba Kazemi; Mohammad Reza Abbaszadegan
Journal:  Iran J Basic Med Sci       Date:  2012-09       Impact factor: 2.699

  7 in total

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