Is There Enough Evidence to Support the Role of Glycosaminoglycans and Proteoglycans in Thoracic Aortic Aneurysm and Dissection?-A Systematic Review

被引:7
作者
Rai, Pratik [1 ]
Robinson, Lucy [1 ]
Davies, Hannah A. [1 ]
Akhtar, Riaz [2 ,3 ]
Field, Mark [3 ,4 ]
Madine, Jillian [1 ,3 ]
机构
[1] Univ Liverpool, Fac Hlth & Life Sci, Inst Syst Mol & Integrat Biol, Dept Biochem & Syst Biol, Liverpool L69 7ZB, Merseyside, England
[2] Univ Liverpool, Sch Engn, Dept Mech Mat & Aerosp Engn, Liverpool L69 3GH, Merseyside, England
[3] Liverpool Ctr Cardiovasc Sci, Liverpool L7 8TX, Merseyside, England
[4] Liverpool Heart & Chest Hosp, Dept Cardiac Surg, Liverpool L14 3PE, Merseyside, England
关键词
thoracic aortic aneurysm; thoracic aortic dissection; proteoglycans; glycosaminoglycans; biomechanics; aorta; ACID-MUCOPOLYSACCHARIDES; EXTRACELLULAR-MATRIX; SULFATED GLYCOSAMINOGLYCANS; GROWTH-FACTOR; HEPARAN-SULFATE; MEDIA; AGE; VERSICAN; WALL; ATHEROSCLEROSIS;
D O I
10.3390/ijms23169200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Altered proteoglycan (PG) and glycosaminoglycan (GAG) distribution within the aortic wall has been implicated in thoracic aortic aneurysm and dissection (TAAD). This review was conducted to identify literature reporting the presence, distribution and role of PGs and GAGs in the normal aorta and differences associated with sporadic TAAD to address the question; is there enough evidence to establish the role of GAGs/PGs in TAAD? 75 studies were included, divided into normal aorta (n = 51) and TAAD (n = 24). There is contradictory data regarding changes in GAGs upon ageing; most studies reported an increase in GAG sub-types, often followed by a decrease upon further ageing. Fourteen studies reported changes in PG/GAG or associated degradation enzyme levels in TAAD, with most increased in disease tissue or serum. We conclude that despite being present at relatively low abundance in the aortic wall, PGs and GAGs play an important role in extracellular matrix maintenance, with differences observed upon ageing and in association with TAAD. However, there is currently insufficient information to establish a cause-effect relationship with an underlying mechanistic understanding of these changes requiring further investigation. Increased PG presence in serum associated with aortic disease highlights the future potential of these biomolecules as diagnostic or prognostic biomarkers.
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页数:18
相关论文
共 87 条
  • [1] Modeling lamellar disruption within the aortic wall using a particle-based approach
    Ahmadzadeh, H.
    Rausch, M. K.
    Humphrey, J. D.
    [J]. SCIENTIFIC REPORTS, 2019, 9 (1)
  • [2] Particle-based computational modelling of arterial disease
    Ahmadzadeh, H.
    Rausch, M. K.
    Humphrey, J. D.
    [J]. JOURNAL OF THE ROYAL SOCIETY INTERFACE, 2018, 15 (149)
  • [3] Biomechanical factors in the biology of aortic wall and aortic valve diseases
    Back, Magnus
    Gasser, T. Christian
    Michel, Jean-Baptiste
    Caligiuri, Giuseppina
    [J]. CARDIOVASCULAR RESEARCH, 2013, 99 (02) : 232 - 241
  • [4] Regulation of glycosaminoglycan structure and atherogenesis
    Ballinger, ML
    Nigro, J
    Frontanilla, KV
    Dart, AM
    Little, PJ
    [J]. CELLULAR AND MOLECULAR LIFE SCIENCES, 2004, 61 (11) : 1296 - 1306
  • [5] Myh11R247C/R247C mutations increase thoracic aorta vulnerability to intramural damage despite a general biomechanical adaptivity
    Bellini, Chiara
    Wang, Shanzhi
    Milewicz, Dianna M.
    Humphrey, Jay D.
    [J]. JOURNAL OF BIOMECHANICS, 2015, 48 (01) : 113 - 121
  • [7] BERTELSEN S, 1960, ACTA PHARMACOL TOX, V16, P250
  • [8] Preliminary Biomarkers for Identification of Human Ascending Thoracic Aortic Aneurysm
    Black, Kendra M.
    Masuzawa, Akihiro
    Hagberg, Robert C.
    Khabbaz, Kamal R.
    Trovato, Mary E.
    Rettagliati, Verna M.
    Bhasin, Manoj K.
    Dillon, Simon T.
    Libermann, Towia A.
    Toumpoulis, Ioannis K.
    Levitsky, Sidney
    McCully, James D.
    [J]. JOURNAL OF THE AMERICAN HEART ASSOCIATION, 2013, 2 (06): : e000138
  • [9] GLYCOSAMINOGLYCAN FRACTIONS FROM HUMAN ARTERIES PRESENTING DIVERSE SUSCEPTIBILITIES TO ATHEROSCLEROSIS HAVE DIFFERENT BINDING AFFINITIES TO PLASMA LDL
    CARDOSO, LEM
    MOURAO, PAS
    [J]. ARTERIOSCLEROSIS AND THROMBOSIS, 1994, 14 (01): : 115 - 124
  • [10] CAREY DJ, 1991, MOL CELL BIOCHEM, V104, P21