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Microcephalic osteodysplastic primordial dwarfism type II is associated with global vascular disease
Angela L Duker1, Dagmar Kinderman2, Christy Jordan3
1Skeletal Dysplasia Program, Division of Orthogenetics, Nemours/Alfred I. duPont Hospital for Children, 1600 Rockland Road, Wilmington, DE, 19803, USA.
Background:
Microcephalic osteodysplastic primordial dwarfism type II (MOPDII) is the most common form of primordial dwarfism, caused by bialleic mutations in the pericentrin gene (PCNT). Aside from its classic features, there are multiple associated medical complications, including a well-documented risk of neurovascular disease. Over the past several years, it has become apparent that additional vascular issues, as well as systemic hypertension and kidney disease may also be related to MOPDII. However, the frequency and extent of the vasculopathy was unclear. To help address this question, a vascular substudy was initiated within our Primordial Dwarfism Registry.
Results:
Medical records from 47 individuals, living and deceased, ranging in age from 3 to 41 years of age were interrogated for this purpose. Of the total group, 64% were diagnosed with moyamoya, intracranial aneurysms, or both. In general, the age at diagnosis for moyamoya was younger than aneurysms, but the risk for neurovascular disease was throughout the shortened lifespan. In addition to neurovascular disease, renal, coronary and external carotid artery involvement are documented. 43% of the total group was diagnosed with hypertension, and 17% had myocardial infarctions. A total of 32% of the entire cohort had some form of chronic kidney disease, with 4% of the total group necessitating a kidney transplant. In addition, 38% had diabetes/insulin resistance. Ages of diagnoses, treatment modalities employed, and location of vasculopathies were notated as available and applicable, as well as frequencies of other comorbidities.
Conclusions:
It is now clear that vascular disease in MOPDII is global and screening of the cardiac and renal vessels is warranted along with close monitoring of blood pressure. We recommend a blood pressure of 110/70 mmHg as a starting point for an upper limit, especially if the individual has a history of neurovascular disease, chronic kidney disease and/or diabetes. Additionally, providers need to be at high alert for the possibility of myocardial infarctions in young adults with MOPDII, so that appropriate treatment can be initiated promptly in an acute situation.
Insights
Microcephalic osteodysplastic primordial dwarfism type II (MOPDII) patients frequently experience widespread vascular issues, including neurovascular, cardiac, and renal complications. Early screening and monitoring for these conditions are crucial for timely intervention and improved patient outcomes.
Area of Science:
- Genetics and Molecular Biology
- Cardiovascular Medicine
- Nephrology
Background:
- Microcephalic osteodysplastic primordial dwarfism type II (MOPDII) is the most common primordial dwarfism, caused by PCNT gene mutations.
- MOPDII is associated with neurovascular disease, but the extent of other vascular complications was unclear.
- A vascular substudy was initiated to investigate systemic vascular involvement in MOPDII.
Purpose of the Study:
- To determine the frequency and extent of vascular disease in individuals with MOPDII.
- To identify associated comorbidities such as hypertension, kidney disease, and diabetes.
Main Methods:
- Retrospective analysis of medical records from 47 MOPDII patients (ages 3-41).
- Interrogation of records for diagnoses of moyamoya, aneurysms, hypertension, myocardial infarctions, and chronic kidney disease.
- Documentation of comorbidities including diabetes/insulin resistance.
Main Results:
- 64% of patients had moyamoya, intracranial aneurysms, or both.
- 43% were diagnosed with hypertension, 17% with myocardial infarctions, and 32% with chronic kidney disease.
- 38% had diabetes/insulin resistance, indicating a high prevalence of systemic vascular and metabolic issues.
Conclusions:
- Vascular disease in MOPDII is global, necessitating screening of cardiac and renal vessels.
- Close blood pressure monitoring is recommended, with an upper limit of 110/70 mmHg.
- Healthcare providers should maintain high alert for myocardial infarctions in young MOPDII adults.
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