Loeys-Dietz Syndrome

Actionability Adult Summary Report

Secondary Findings in Adult Subjects. Non-diagnostic, excludes newborn screening & prenatal testing/screening.

• Mode(s) of Inheritance: Autosomal Dominant
• Literature Search: 03/20/2015
• Curation Status: Released - Under Revision (2.1.0)

Assertions and Scores

Actionability Assertions

Gene	Condition (MONDO ID)	OMIM ID	Final Assertion
No assertions found.

Actionability Assertion Rationale

• This topic was initially scored prior to development of the process for making actionability assertions. The Actionability Working Group decided to defer making an assertion until after the topic could be reviewed through the update process.

Actionability Scores

Outcome / Intervention Pair	Severity	Likelihood	Effectiveness	Nature of Intervention	Total Score
Clinically Significant Aortic Aneurysm / Surveillance	3	3C	3B	3	12CB
Aortic Dilation Progression / Pharmacotherapy, including beta-blockers and angiotensin II receptor blockers	3	3C	2B	3	11CB

Severity of Outcome

Prevalence of the Genetic Condition

The prevalence of Loeys-Dietz syndrome (LDS) is unknown.

Clinical Features (Signs / symptoms)

LDS represents a continuum of clinical presentation. LDS is mainly characterized by vascular (cerebral, thoracic, and abdominal arterial aneurysms and/or dissections; arterial tortuousity) and skeletal (pectus deformity, scoliosis, joint laxity, arachnodactyly, club foot) manifestations. Patients may also display craniofacial (widely spaced eyes, bifid uvula, cleft palate, and craniosynostosis) and cutaneous (translucent skin, easy bruising, dystrophic scars) manifestations.Pathogenic variants in TGFBR1 and TGFBR2 are associated with 2 types of LDS that are clinically indistinguishable: Type I (LDS1; ~70% of cases) with vascular, skeletal, cutaneous, and craniofacial manifestations and Type II (LDS2; ~20% of cases) with the systemic manifestations of LDS1 but minimal or absent craniofacial manifestations. SMAD3 pathogenic variants are associated with Type III (LDS3; ~5% of cases), which overlaps with Types I and II, but is characterized by an increased risk of osteoarthritis. TGFB2 is associated with Type IV (LDS4; ~1% of cases), which has classic LDS features but milder phenotype, with club feet and mitral valve disease as the most recurrent features. TGFB3 is associated with Type V (LDS5), which has the typical LDS features of aortic aneurysms and other systemic features, but no striking aortic or arterial tortuosity and no strong evidence for early aortic dissection.

Natural History (Important subgroups & survival / recovery)

The vascular disease in LDS is aggressive, with a mean age of death of 26 years. However, recent studies indicate a higher survival rate (80% at age 60) and later age of onset (31 years for LDS1 and 46 years for LDS2) than previous reported. A study of 45 LDS3 patients indicated an age of onset range of 18 to 61 years for joint complaints and 20 to 66 years for cardiovascular abnormalities. A study of 2 LDS4 families reported a median age of aortic disease of 35 years. A study of 12 individuals with LDS5 indicated that 7 presented with aneurysms and dissections between the ages of 40 and 68. There is a high incidence of pregnancy-related complications, including aortic dissection/rupture and uterine rupture during pregnancy or delivery and aortic dissection/rupture in the immediate postpartum period. No ethnic/racial or gender difference has been reported, though there is evidence that males have a greater risk of aortic events and an earlier age of onset of vascular disease than females.

Likelihood of Outcome

Mode of Inheritance

Autosomal Dominant

Prevalence of Genetic Variants

Unknown

Information on the prevalence if genetic variants associated with LDS was unavailable.

Penetrance (Includes any high-risk racial or ethnic subgroups)

>= 40 %

While non-penetrance in LDS has been documented, 98% of individuals have aortic root aneurysms that lead to aortic dissection and 53% develop aneurysms of other vessels.

Tier 4

Relative Risk (Includes any high-risk racial or ethnic subgroups)

Unknown

Information on relative risk was unavailable.

Expressivity

Identical mutations in TGFBR1 and TGFBR2 can lead to either LDS Type I or II. Intrafamilial clinical variability has been noted.

Tier 4

Intervention Effectiveness

Patient Management

Prophylactic surgical repair is typically recommended at an aortic diameter of > 4.2 cm, but this threshold can vary depending on rate of expansion. Timely repair of aortic aneurysms prolongs survival and approaches that of age-matched controls in patients with Marfan syndrome; however, evidence on effectiveness was not provided for patients with LDS.

Tier 2

Beta-blockers or other medications can be used to reduce hemodynamic stress.

Tier 4

Specifically, the use of an angiotensin II receptor blocker (ARB; e.g., losartan) in addition to beta-blockers has been proposed for Marfan syndrome (MFS), a recommendation that may also apply to LDS. However, data on the effectiveness of beta blockers and ARBs is not available for LDS. A systematic review of beta blocker, angiotensin-converting enzyme inhibitor, and ARB use in MFS concluded that these medications slowed the progression of aortic dilation. Three of the included studies showed that the treatment group’s aortic dilation progressed by roughly 1mm/year less than the non-treatment group, though no information was provided on how this impacted clinical outcomes.

Tier 1

In addition, two randomized trials in patients with MFS reported reductions in aortic root dilation rate with ARB added to beta blockers at three-year follow-up, indicating that treatment with beta blockers and ARB may be more effective than beta blockers alone. In contrast, a double-blind randomized trial found no significant difference between ARB and placebo on aortic root dilation rate at median 3.5-year follow-up, with most patients in both treatment groups also on beta blockers (86%).

Tier 5

Individuals with either a TGFBR1 or TGFBR2 mutation should be taught the signs and symptoms of aortic dissection and should consider wearing a medical alert bracelet.

Tier 2

Prophylactic antibiotics for any invasive procedure including dentistry are recommended.

Tier 2

Because of a high risk of cervical spine instability, an x-ray of the cervical spine should be performed prior to intubation or any other procedure involving manipulation of the neck. Surgical fixation of the cervical spine may be necessary to prevent damage to the spinal cord.

Tier 4

Patients should undergo radiographs to detect skeletal manifestations, such as scoliosis, that may require attention by an orthopedist

Tier 4

Patients should undergo an eye examination by an ophthalmologist with expertise in connective tissue disorders to assess for retinal detachment and blue sclerae.

Tier 4

During pregnancy there is a high incidence of pregnancy-related complications including uterine rupture, hemorrhage, and death. Thus women should be monitored by a high-risk obstetric clinic and undergo more frequent aortic imaging during pregnancy and in the weeks following delivery.

Tier 4

Surveillance

Patients should undergo complete aortic imaging at initial diagnosis and 6 months later to determine the rate of aortic enlargement followed by regular imaging, followed by echocardiograms annually or at least every 6 months if aortic root dilation is detected.

Tier 2

Patients should have yearly magnetic resonance imaging from the cerebrovascular circulation to the pelvis.

Tier 1

Circumstances to Avoid

Patients should avoid contact sports, competitive sports, and isometric exercise; agents that stimulate the cardiovascular system including routine use of decongestants; activities that cause joint injury or pain; and for individuals at risk for recurrent pneumothorax, breathing against a resistance (e.g., playing a brass instrument) or positive pressure ventilation (e.g., scuba diving).

Tier 4

Nature of Intervention

Nature of Intervention

The identified interventions involve medications with potential side effects and invasive prophylactic surgery, which is likely associated with high risk and morbidity.

Context: Adult

Chance to Escape Clinical Detection

The major source of morbidity and early mortality in LDS is related to cardiovascular outcomes, such as predisposition for aortic dissection and rupture, which would likely not be detected through routine clinical care.

Context: Adult

Tier 4

Gene Condition Association

Gene			Condition Associations
			OMIM Identifier	Primary MONDO Identifier	Additional MONDO Identifiers

References List

Arslan-Kirchner M, Epplen JT, Faivre L, Jondeau G, Schmidtke J, De Paepe A, Loeys B. (2011) Clinical utility gene card for: Loeys-Dietz syndrome (TGFBR1/2) and related phenotypes. European journal of human genetics : EJHG. 19(10).

BL Loeys, HC Dietz. Loeys-Dietz Syndrome. (2008) [Updated Jul 11 2013]. In: RA Pagon, MP Adam, HH Ardinger, et al., editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2026. Available from: https://www.ncbi.nlm.nih.gov/books/NBK1133/

Boodhwani M, Andelfinger G, Leipsic J, Lindsay T, McMurtry MS, Therrien J, Siu SC. (2014) Canadian Cardiovascular Society position statement on the management of thoracic aortic disease. The Canadian journal of cardiology. 30(6):577-89.

Chiu HH, Wu MH, Wang JK, Lu CW, Chiu SN, Chen CA, Lin MT, Hu FC. (2013) Losartan added to beta-blockade therapy for aortic root dilation in Marfan syndrome: a randomized, open-label pilot study. Mayo Clinic proceedings. 88(3):271-6.

Groenink M, den Hartog AW, Franken R, Radonic T, de Waard V, Timmermans J, Scholte AJ, van den Berg MP, Spijkerboer AM, Marquering HA, Zwinderman AH, Mulder BJ. (2013) Losartan reduces aortic dilatation rate in adults with Marfan syndrome: a randomized controlled trial. European heart journal. 34(45):3491-500.

Hiratzka LF, Bakris GL, Beckman JA, Bersin RM, Carr VF, Casey DE Jr, Eagle KA, Hermann LK, Isselbacher EM, Kazerooni EA, Kouchoukos NT, Lytle BW, Milewicz DM, Reich DL, Sen S, Shinn JA, Svensson LG, Williams DM. (2010) 2010 ACCF/AHA/AATS/ACR/ASA/SCA/SCAI/SIR/STS/SVM Guidelines for the diagnosis and management of patients with thoracic aortic disease. A Report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines, American Association for Thoracic Surgery, American College of Radiology,American Stroke Association, Society of Cardiovascular Anesthesiologists, Society for Cardiovascular Angiography and Interventions, Society of Interventional Radiology, Society of Thoracic Surgeons,and Society for Vascular Medicine. Journal of the American College of Cardiology. 55(14):e27-e129.

LOEYS-DIETZ SYNDROME 1; LDS1. Online Medelian Inheritance in Man, OMIM®. Johns Hopkins University, Baltimore, MD. MIM: 609192, (2017) World Wide Web URL: http://omim.org/

LOEYS-DIETZ SYNDROME 2; LDS2. Online Medelian Inheritance in Man, OMIM®. Johns Hopkins University, Baltimore, MD. MIM: 610168, (2017) World Wide Web URL: http://omim.org/

LOEYS-DIETZ SYNDROME 3; LDS3. Online Medelian Inheritance in Man, OMIM®. Johns Hopkins University, Baltimore, MD. MIM: 613795, (2016) World Wide Web URL: http://omim.org/

LOEYS-DIETZ SYNDROME 4; LDS4. Online Medelian Inheritance in Man, OMIM®. Johns Hopkins University, Baltimore, MD. MIM: 614816, (2014) World Wide Web URL: http://omim.org/

LOEYS-DIETZ SYNDROME 5; LDS5. Online Medelian Inheritance in Man, OMIM®. Johns Hopkins University, Baltimore, MD. MIM: 615582, (2017) World Wide Web URL: http://omim.org/

Milleron O, Arnoult F, Ropers J, Aegerter P, Detaint D, Delorme G, Attias D, Tubach F, Dupuis-Girod S, Plauchu H, Barthelet M, Sassolas F, Pangaud N, Naudion S, Thomas-Chabaneix J, Dulac Y, Edouard T, Wolf JE, Faivre L, Odent S, Basquin A, Habib G, Collignon P, Boileau C, Jondeau G. (2015) Marfan Sartan: a randomized, double-blind, placebo-controlled trial. European heart journal. 36(32):2160-6.

Pyeritz RE. (2012) Evaluation of the adolescent or adult with some features of Marfan syndrome. Genetics in medicine : official journal of the American College of Medical Genetics. 14(1):171-7.

Svensson LG, Adams DH, Bonow RO, Kouchoukos NT, Miller DC, O'Gara PT, Shahian DM, Schaff HV, Akins CW, Bavaria JE, Blackstone EH, David TE, Desai ND, Dewey TM, D'Agostino RS, Gleason TG, Harrington KB, Kodali S, Kapadia S, Leon MB, Lima B, Lytle BW, Mack MJ, Reardon M, Reece TB, Reiss GR, Roselli EE, Smith CR, Thourani VH, Tuzcu EM, Webb J, Williams MR. (2013) Aortic valve and ascending aorta guidelines for management and quality measures. The Annals of thoracic surgery. 95(6 Suppl):S1-66.

Thakur V, Rankin KN, Hartling L, Mackie AS. (2013) A systematic review of the pharmacological management of aortic root dilation in Marfan syndrome. Cardiology in the young. 23(4):568-81.