Abnormally increased carotid intima media-thickness and elasticity in patients with Morquio A disease

Raymond Y Wang, Kyle D Rudser, Donald R Dengel, Nicholas Evanoff, Julia Steinberger, Nina Movsesyan, Robert Garrett, Katherine Christensen, Deborah Boylan, Stephen R Braddock, Marwan Shinawi, Qi Gan, Adriana M Montaño, Raymond Y Wang, Kyle D Rudser, Donald R Dengel, Nicholas Evanoff, Julia Steinberger, Nina Movsesyan, Robert Garrett, Katherine Christensen, Deborah Boylan, Stephen R Braddock, Marwan Shinawi, Qi Gan, Adriana M Montaño

Abstract

Background: Cardiovascular disease frequently causes morbidity and mortality in mucopolysaccharidoses (MPS); however, cardiovascular anatomy and dysfunction in MPS IVA (Morquio A disease) is not well described. Consequently, the study aimed to compare carotid artery structure and elasticity of MPS IVA patients with other MPS patients and healthy control subjects, and quantitate frequency of MPS IVA cardiac structural and functional abnormalities.

Methods: Prospective, multi-center echocardiogram and carotid ultrasound evaluations of 12 Morquio A patients were compared with other MPS and healthy control subjects. Average differences between groups were adjusted for age, sex, and height with robust variance estimation for confidence intervals and P-values.

Results: Morquio A patients demonstrated significantly higher (P < 0.001) adjusted carotid intima-media thickness (cIMT), mean (SD) of 0.56 mm (0.03) compared to control subjects, 0.44 mm (0.04). The Morquio A cohort had significantly greater adjusted carotid elasticity (carotid cross-sectional compliance + 43%, P < 0.001; carotid incremental elastic modulus - 33%, P = 0.003) than control subjects and other MPS patients. Aortic root dilatation was noted in 56% of the Morquio A cohort, which also had highly prevalent mitral (73%) and aortic (82%) valve thickening, though hemodynamically significant valve dysfunction was less frequent (9%).

Conclusions: Increased carotid elasticity in Morquio A patients is an unexpected contrast to the reduced elasticity observed in other MPS. These Morquio A cIMT findings corroborate MPS IVA arterial post-mortem reports and are consistent with cIMT of other MPS. Aortic root dilatation in Morquio A indicates arterial elastin dysfunction, but their carotid hyperelasticity indicates other vascular intima/media components, such as proteoglycans, may also influence artery function. Studying MPS I and IVA model systems may uniquely illuminate the function of glycosaminoglycan-bearing proteoglycans in arterial health.

Keywords: Cardiovascular disease; Carotid ultrasound; Intima media thickness; Morquio A disease; Mucopolysaccharidosis IVA.

Conflict of interest statement

The authors declare that they have no competing interests.

References

    1. Neufeld E, Muenzer J. The Mucopolysaccharidoses. In: Scriver C, Beaudet AL, Sly WS, Valle D, editors. The metabolic and molecular bases of inherited diseases. 8. New York: McGraw Hill; 2001.
    1. Montaño AM, Tomatsu S, Gottesman GS, Smith M, Orii T. International Morquio a registry: clinical manifestation and natural course of Morquio a disease. J Inherit Metab Dis. 2007;30(2):165–174. doi: 10.1007/s10545-007-0529-7.
    1. Fesslova V, Corti P, Sersale G, Rovelli A, Russo P, Mannarino S, et al. The natural course and the impact of therapies of cardiac involvement in the mucopolysaccharidoses. Cardiol Young. 2009;19(2):170–178. doi: 10.1017/S1047951109003576.
    1. John RM, Hunter D, Swanton RH. Echocardiographic abnormalities in type IV mucopolysaccharidosis. Arch Dis Child. 1990;65(7):746–749. doi: 10.1136/adc.65.7.746.
    1. Lin HY, Chuang CK, Chen MR, Lin SM, Hung CL, Chang CY, et al. Cardiac structure and function and effects of enzyme replacement therapy in patients with mucopolysaccharidoses I, II, IVA and VI. Mol Genet Metab. 2016;117(4):431–437. doi: 10.1016/j.ymgme.2016.02.003.
    1. Braunlin EA, Harmatz PR, Scarpa M, Furlanetto B, Kampmann C, Loehr JP, et al. Cardiac disease in patients with mucopolysaccharidosis: presentation, diagnosis and management. J Inherit Metab Dis. 2011;34(6):1183–1197. doi: 10.1007/s10545-011-9359-8.
    1. Kampmann C, Abu-Tair T, Gokce S, Lampe C, Reinke J, Mengel E, et al. Heart and cardiovascular involvement in patients with Mucopolysaccharidosis type IVA (Morquio-a syndrome) PLoS One. 2016;11(9):e0162612. doi: 10.1371/journal.pone.0162612.
    1. Yasuda E, Fushimi K, Suzuki Y, Shimizu K, Takami T, Zustin J, et al. Pathogenesis of Morquio a syndrome: an autopsied case reveals systemic storage disorder. Mol Genet Metab. 2013;109(3):301–311. doi: 10.1016/j.ymgme.2013.04.009.
    1. Berni A, Giuliani A, Tartaglia F, Tromba L, Sgueglia M, Blasi S, et al. Effect of vascular risk factors on increase in carotid and femoral intima-media thickness. Identification of a risk scale. Atherosclerosis. 2011;216(1):109–114. doi: 10.1016/j.atherosclerosis.2011.01.034.
    1. Wang RY, Covault KK, Halcrow EM, Gardner AJ, Cao X, Newcomb RL, et al. Carotid intima-media thickness is increased in patients with mucopolysaccharidoses. Mol Genet Metab. 2011;104(4):592–596. doi: 10.1016/j.ymgme.2011.09.004.
    1. Wang RY, Rudser KD, Dengel DR, Braunlin EA, Steinberger J, Jacobs DR, et al. The Carotid Intima-Media Thickness and Arterial Stiffness of Pediatric Mucopolysaccharidosis Patients Are Increased Compared to Both Pediatric and Adult Controls. Int J Mol Sci. 2017;18(3).
    1. Wang RY, Braunlin EA, Rudser KD, Dengel DR, Metzig AM, Covault KK, et al. Carotid intima-media thickness is increased in patients with treated mucopolysaccharidosis types I and II, and correlates with arterial stiffness. Mol Genet Metab. 2014;111(2):128–132. doi: 10.1016/j.ymgme.2013.11.001.
    1. Dung VC, Tomatsu S, Montano AM, Gottesman G, Bober MB, Mackenzie W, et al. Mucopolysaccharidosis IVA: correlation between genotype, phenotype and keratan sulfate levels. Mol Genet Metab. 2013;110(1–2):129–138. doi: 10.1016/j.ymgme.2013.06.008.
    1. Sukegawa K, Nakamura H, Kato Z, Tomatsu S, Montaño AM, Fukao T, et al. Biochemical and structural analysis of missense mutations in N-acetylgalactosamine-6-sulfate sulfatase causing mucopolysaccharidosis IVA phenotypes. Hum Mol Genet. 2000;9(9):1283–1290. doi: 10.1093/hmg/9.9.1283.
    1. Adzhubei IA, Schmidt S, Peshkin L, Ramensky VE, Gerasimova A, Bork P, et al. A method and server for predicting damaging missense mutations. Nat Methods. 2010;7(4):248–249. doi: 10.1038/nmeth0410-248.
    1. Morrone A, Tylee KL, Al-Sayed M, Brusius-Facchin AC, Caciotti A, Church HJ, et al. Molecular testing of 163 patients with Morquio a (Mucopolysaccharidosis IVA) identifies 39 novel GALNS mutations. Mol Genet Metab. 2014;112(2):160–170. doi: 10.1016/j.ymgme.2014.03.004.
    1. Morrone A, Caciotti A, Atwood R, Davidson K, Du C, Francis-Lyon P, et al. Morquio a syndrome-associated mutations: a review of alterations in the GALNS gene and a new locus-specific database. Hum Mutat. 2014;35(11):1271–1279.
    1. Tomatsu S, Montano AM, Nishioka T, Gutierrez MA, Pena OM, Tranda Firescu GG, et al. Mutation and polymorphism spectrum of the GALNS gene in mucopolysaccharidosis IVA (Morquio a) Hum Mutat. 2005;26(6):500–512. doi: 10.1002/humu.20257.
    1. Ogawa T, Tomatsu S, Fukuda S, Yamagishi A, Rezvi GM, Sukegawa K, et al. Mucopolysaccharidosis IVA: screening and identification of mutations of the N-acetylgalactosamine-6-sulfate sulfatase gene. Hum Mol Genet. 1995;4(3):341–349. doi: 10.1093/hmg/4.3.341.
    1. Wang Z, Zhang W, Wang Y, Meng Y, Su L, Shi H, et al. Mucopolysaccharidosis IVA mutations in Chinese patients: 16 novel mutations. J Hum Genet. 2010;55(8):534–540. doi: 10.1038/jhg.2010.65.
    1. Rivera-Colon Y, Schutsky EK, Kita AZ, Garman SC. The structure of human GALNS reveals the molecular basis for mucopolysaccharidosis IV a. J Mol Biol. 2012;423(5):736–751. doi: 10.1016/j.jmb.2012.08.020.
    1. Tomatsu S, Fukuda S, Cooper A, Wraith JE, Ferreira P, Di Natale P, et al. Fourteen novel mucopolysaccharidosis IVA producing mutations in GALNS gene. Hum Mutat. 1997;10(5):368–375. doi: 10.1002/(SICI)1098-1004(1997)10:5<368::AID-HUMU6>;2-B.
    1. Tapiero-Rodriguez SM, Acosta Guio JC, Porras-Hurtado GL, Garcia N, Solano M, Pachajoa H, et al. Determination of genotypic and clinical characteristics of Colombian patients with mucopolysaccharidosis IVA. Appl Clin Genet. 2018;11:45–57. doi: 10.2147/TACG.S141881.
    1. Lew V, Pena L, Edwards R, Wang RY. Cardiovascular histopathology of a 11-year old with Mucopolysaccharidosis VII demonstrates fibrosis, macrophage infiltration, and arterial luminal stenosis. JIMD Rep. 2018;39:31–37. doi: 10.1007/8904_2017_43.
    1. Metcalf JA, Linders B, Wu S, Bigg P, O'Donnell P, Sleeper MM, et al. Upregulation of elastase activity in aorta in mucopolysaccharidosis I and VII dogs may be due to increased cytokine expression. Mol Genet Metab. 2010;99(4):396–407. doi: 10.1016/j.ymgme.2009.12.003.
    1. Kiotsekoglou A, Moggridge JC, Kapetanakis V, Newey VR, Kourliouros A, Mullen MJ, et al. Assessment of carotid compliance using real time vascular ultrasound image analysis in Marfan syndrome. Echocardiography. 2009;26(4):441–451. doi: 10.1111/j.1540-8175.2008.00813.x.
    1. Poswar FO, de Souza CFM, Giugliani R, Baldo G. Aortic root dilatation in patients with mucopolysaccharidoses and the impact of enzyme replacement therapy. Heart Vessels. 2019;34:290-5.
    1. Hendriksz CJ, Berger KI, Giugliani R, Harmatz P, Kampmann C, Mackenzie WG, et al. International guidelines for the management and treatment of Morquio a syndrome. Am J Med Genet A. 2015;167A(1):11–25. doi: 10.1002/ajmg.a.36833.
    1. Pizarro C, Davies RR, Theroux M, Spurrier EA, Averill LW, Tomatsu S. Surgical reconstruction for severe tracheal obstruction in Morquio a syndrome. Ann Thorac Surg. 2016;102(4):e329–e331. doi: 10.1016/j.athoracsur.2016.02.113.
    1. Drummond JC, Krane EJ, Tomatsu S, Theroux MC, Lee RR. Paraplegia after epidural-general anesthesia in a Morquio patient with moderate thoracic spinal stenosis. Can J Anaesth. 2015;62(1):45–49. doi: 10.1007/s12630-014-0247-1.
    1. Yla-Herttuala S, Solakivi T, Hirvonen J, Laaksonen H, Mottonen M, Pesonen E, et al. Glycosaminoglycans and apolipoproteins B and A-I in human aortas. Chemical and immunological analysis of lesion-free aortas from children and adults. Arteriosclerosis. 1987;7(4):333–340. doi: 10.1161/01.ATV.7.4.333.
    1. Wasty F, Alavi MZ, Moore S. Distribution of glycosaminoglycans in the intima of human aortas: changes in atherosclerosis and diabetes mellitus. Diabetologia. 1993;36(4):316–322. doi: 10.1007/BF00400234.
    1. Wight TN, Merrilees MJ. Proteoglycans in atherosclerosis and restenosis: key roles for versican. Circ Res. 2004;94(9):1158–1167. doi: 10.1161/01.RES.0000126921.29919.51.
    1. Montaño AM, Tomatsu S, Brusius A, Smith M, Orii T. Growth charts for patients affected with Morquio a disease. Am J Med Genet A. 2008;146A(10):1286–1295. doi: 10.1002/ajmg.a.32281.
    1. Marlatt KL, Kelly AS, Steinberger J, Dengel DR. The influence of gender on carotid artery compliance and distensibility in children and adults. J Clin Ultrasound. 2013;41(6):340–346. doi: 10.1002/jcu.22015.
    1. R_Core_Team. R: A language and environment for statistical computing. Vienna; 2018. Available online at .

Source: PubMed

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