Plasma Fibroblast Growth Factor 23 Is Elevated in Pediatric Primary Hypertension
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Published on: October 5, 2010
Yao Lin1, Lin Shi1, Yanyan Liu1
1Department of Pediatric Cardiology, Children's Hospital, Capital Institute of Pediatrics, Beijing, China.
Insights
Fibroblast growth factor 23 (FGF 23) levels are higher in children with hypertension. Elevated FGF 23 is linked to abnormal cardiac geometry in these young patients.
Area of Science:
- Pediatric Cardiology
- Endocrinology
- Nephrology
Background:
- Fibroblast growth factor 23 (FGF 23) is an endocrine hormone crucial for phosphate and vitamin D homeostasis.
- Elevated FGF 23 is associated with cardiovascular disease and hypertension in adults.
- FGF 23 levels in hypertensive children remain undocumented.
Purpose of the Study:
- To investigate and compare blood FGF 23 levels in children with primary hypertension versus healthy controls.
- To analyze FGF 23 levels in hypertensive children based on cardiac geometry, hypertension stage, insulin levels, and weight.
Main Methods:
- A comparative study involving 98 children with primary hypertension and 37 controls.
- Blood FGF 23 levels were measured and analyzed.
- Subgroup analysis was performed on hypertensive children based on clinical parameters.
Main Results:
- Hypertensive children exhibited significantly higher FGF 23 levels compared to controls (median 48.99 vs. 41.72, p = 0.0002).
- Elevated FGF 23 was significantly associated with abnormal cardiac geometry in hypertensive children (p = 0.0085).
- No significant differences in FGF 23 were found based on obesity, hypertension stage, or insulin levels.
Conclusions:
- This study demonstrates, for the first time, elevated FGF 23 levels in hypertensive children.
- Abnormal cardiac geometry in hypertensive children is linked to higher FGF 23.
- Further research is warranted to explore FGF 23's role and potential therapeutic targeting in pediatric hypertension.
Abstract:
Fibroblast growth factor 23 (FGF 23), an endocrine hormone regulating the homeostasis of phosphate and vitamin D, has been shown to play a role in cardiovascular disease. Increased blood FGF 23 is found to be associated with elevated blood pressure in adults. However, measurement of FGF 23 in hypertensive children has not been documented. In this study, a total of 98 children with primary hypertension and 37 controls were recruited, and blood FGF 23 was comparatively investigated. Additionally, FGF 23 levels were compared between the subgroups of patients after hypertensive children were sub-grouped according to their cardiac geometry, hypertension stages, insulin levels, and weight. The case group had a FGF 23 level of 48.99 (16.42), expressed as the median (the interquartile range), significantly higher than the 41.72 (7.05) from the control group (p = 0.0002). While no remarkable differences were observed in FGF 23 levels between non-obese and obese hypertensive children, between patients with stage 1 and stage 2 hypertension, or between patients with normal and high insulin levels; hypertensive children with abnormal cardiac geometry had significantly higher levels of FGF 23 than patients with normal cardiac geometry (p = 0.0085). Our data revealed for the first time that hypertensive children have higher levels of FGF 23. Further studies are needed to examine if lowering FGF 23 improves the cardiac geometry in hypertensive children with higher FGF 23.
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