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Familial risk of pediatric chronic rhinosinusitis
Quinn Orb1, Karen Curtin2,3, Gretchen M Oakley1
1Division of Otolaryngology, University of Utah School of Medicine.
Insights
Children with chronic rhinosinusitis (CRS) have a significantly increased risk of developing the condition if they have affected relatives. This familial link suggests a genetic component to CRS, warranting further research into its causes.
Area of Science:
- Otolaryngology
- Genetics
- Epidemiology
Background:
- Chronic rhinosinusitis (CRS) is a common condition affecting both children and adults.
- The etiology of CRS is complex, involving genetic predisposition and environmental factors.
- Understanding familial risk can provide insights into the underlying causes of CRS.
Purpose of the Study:
- To investigate the familial risk of developing chronic rhinosinusitis (CRS) in relatives of pediatric patients diagnosed with CRS.
- To quantify the recurrence risk across different degrees of familial relationship.
Main Methods:
- Retrospective observational cohort study utilizing a unique genealogical database linked to medical records.
- Identified pediatric CRS cases (≤12 years old) from 1996-2011.
- Calculated familial recurrence risks using Cox models and compared them to population-based matched controls.
Main Results:
- Siblings of pediatric CRS patients showed a 57.5-fold increased risk of also having pediatric CRS.
- First cousins had a 9.0-fold increased risk, and second cousins had a 2.9-fold increased risk.
- First-degree and second-degree relatives, including parents, demonstrated a significantly increased risk of adult CRS.
Conclusions:
- A significant familial risk for chronic rhinosinusitis (CRS) is confirmed in the largest population study to date.
- Increased risk in parents suggests a genetic component, though one affected parent was more common than two.
- Further research into the genetic basis and environmental interactions of CRS is needed for targeted treatments.
Objectives/Hypothesis:
To determine the risk of chronic rhinosinusitis (CRS) in relatives of children with a diagnosis of CRS.
Study Design:
Retrospective observational cohort study with population-based matched controls.
Methods:
A unique genealogical database linked to medical records was used to identify subjects ≤12 years old with a diagnosis of CRS from 1996 to 2011. The familial recurrence risks of CRS in first- through fifth-degree relatives of probands were calculated using Cox models and compared to controls randomly selected from the Utah population and matched 10:1 on sex and birth year.
Results:
We identified 496 pediatric patients with CRS. Siblings of patients with CRS demonstrated a 57.5-fold increased risk (P < 10(-8) ) of also having pediatric CRS. First cousins had a 9.0-fold increased risk (P < 10(-3) ) and second cousins had a 2.9-fold increased risk (P = .002) of pediatric CRS. First-degree relatives, second-degree relatives, and first cousins of pediatric cases demonstrated a significant increased risk of having adult CRS. Parents of probands demonstrated a 5.6-fold increased risk (P < 10(-15) ). Fifty-five probands had one affected parent versus three probands with two affected parents.
Conclusions:
In the largest population study to date of children with CRS, a significant familial risk is confirmed. Parents of probands were also at increased risk, although it was much more likely for one parent to be affected than both, suggesting a genetic component of the disease. Further understanding of the genetic basis of CRS and its interplay with environmental factors could clarify the etiology and lead to more effective targeted treatments.
Level Of Evidence:
3b Laryngoscope, 126:739-745, 2016.
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