Background: Costello syndrome is a rare genetic condition characterized by coarse facies, short stature, loose folds of skin especially on hands and feet, severe feeding difficulties and failure to thrive. Other features include cardiac anomalies, developmental disability and increased risk of neoplasms. Given the link between oxidative stress (OS) and carcinogenesis, we tested the hypothesis that OS occurs in this syndrome, supposing its role both in cancer development and in other clinical features. Patients and Methods: We describe four cases with Costello syndrome in which we verified the presence of OS by measuring a redox biomarker profile including total hydroperoxides, nonprotein-bound iron, advanced oxidation protein products, thyols, carbonyl groups and isoprostanes. Thus, we introduced an antioxidant agent, namely potassium ascorbate with ribose (PAR) into the therapy and monitored the redox profile every three months to verify its efficacy. Results: A progressive decrease in OS biomarkers occurred, together with an improvement in the clinical features of the patients. Conclusion: OS was proven in all four cases of Costello syndrome. The antioxidant therapy with PAR demonstrated positive effects. These promising results need further research to confirm the relevance of OS and the efficacy of PAR therapy in Costello syndrome.
机构:
Massachusetts Gen Hosp, Serv Pediat, Genet & Teratol Unit, Boston, MA 02114 USAMassachusetts Gen Hosp, Serv Pediat, Genet & Teratol Unit, Boston, MA 02114 USA
Lin, A
Harding, C
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机构:Massachusetts Gen Hosp, Serv Pediat, Genet & Teratol Unit, Boston, MA 02114 USA
Harding, C
Silberbach, M
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机构:Massachusetts Gen Hosp, Serv Pediat, Genet & Teratol Unit, Boston, MA 02114 USA
Silberbach, M
JOURNAL OF PEDIATRICS,
2004,
144
(01):
: 135
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135
机构:
Cincinnati Childrens Hosp Med Ctr, Div Human Genet, Cincinnati, OH 45229 USA
Univ Cincinnati, Coll Med, Dept Pediat, Cincinnati, OH USACincinnati Childrens Hosp Med Ctr, Div Human Genet, Cincinnati, OH 45229 USA
Weaver, K. Nicole
Care, Marguerite
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机构:
Univ Cincinnati, Coll Med, Dept Pediat, Cincinnati, OH USA
Dept Radiol, Cincinnati, OH USACincinnati Childrens Hosp Med Ctr, Div Human Genet, Cincinnati, OH 45229 USA
Care, Marguerite
Wakefield, Emily
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机构:
Cincinnati Childrens Hosp Med Ctr, Div Human Genet, Cincinnati, OH 45229 USACincinnati Childrens Hosp Med Ctr, Div Human Genet, Cincinnati, OH 45229 USA
Wakefield, Emily
Zarate, Yuri A.
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Univ Arkansas Med Sci, Sect Genet & Metab, Little Rock, AR 72205 USACincinnati Childrens Hosp Med Ctr, Div Human Genet, Cincinnati, OH 45229 USA
Zarate, Yuri A.
Skoch, Jesse
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机构:
Univ Cincinnati, Coll Med, Dept Surg, Cincinnati, OH USACincinnati Childrens Hosp Med Ctr, Div Human Genet, Cincinnati, OH 45229 USA
Skoch, Jesse
Gripp, Karen W.
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AI DuPont Hosp Children Nemours, Div Med Genet, Delaware, OH USACincinnati Childrens Hosp Med Ctr, Div Human Genet, Cincinnati, OH 45229 USA
Gripp, Karen W.
Prada, Carlos E.
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Cincinnati Childrens Hosp Med Ctr, Div Human Genet, Cincinnati, OH 45229 USA
Univ Cincinnati, Coll Med, Dept Pediat, Cincinnati, OH USA
Ann & Robert Lurie Childrens Hosp Chicago, Div Genet Birth Defects & Metab, Chicago, IL USACincinnati Childrens Hosp Med Ctr, Div Human Genet, Cincinnati, OH 45229 USA