Key result
Pulmonary hypertension is a common comorbidity in individuals with Down syndrome, frequently driven by multifactorial etiologies such as congenital heart disease and developmental lung disease.
Why the study?
Persons with Down syndrome have an increased reported incidence of pulmonary hypertension, but there are few large-scale, prospective, lifetime cohort studies detailing its impact.
This review highlights that pulmonary hypertension in Down syndrome is multifactorial, requiring comprehensive screening and multidisciplinary management.
Supports comprehensive screening in Down syndrome; leaves open prospective validation of multidisciplinary management.
Persons with Down syndrome (DS) have an increased reported incidence of pulmonary hypertension (PH). A majority of those with PH have associations with congenital heart disease (CHD) or persistent pulmonary hypertension of the newborn (PPHN); however, there are likely multifactorial contributions that include respiratory comorbidities. PH appears to be most commonly identified early in life, although respiratory challenges may contribute to a later diagnosis or even a recurrence of previously resolved PH in this population. Currently there are few large-scale, prospective, lifetime cohort studies detailing the impact PH has on the population with DS. This review will attempt to summarize the epidemiology and characteristics of PH in this population. This article will additionally review current known and probable risk factors for developing PH, review pathophysiologic mechanisms of disease in the population with DS, and evaluate current screening and management recommendations while suggesting areas for additional or ongoing clinical, translational, and basic science research.
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Bush et al. (2022) conducted a review in Pulmonary Hypertension in Down Syndrome. Pulmonary hypertension is a common comorbidity in individuals with Down syndrome, frequently driven by multifactorial etiologies such as congenital heart disease and developmental lung disease.
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