Background: Individuals with congenital adrenal hyperplasia (CAH) require glucocorticoid therapy to replace cortisol and to control androgen excess. We sought to evaluate the effects of glucocorticoid therapy on cardiovascular and metabolic outcomes in individuals with CAH.Methods: We searched bibliographical databases through January 2016 for studies evaluating cardiovascular risk factors in individuals with CAH treated with glucocorticoids compared with controls without CAH. We used a random-effects model to synthesize quantitative data.Results: We included 20 observational studies (14 longitudinal, six cross-sectional) with a moderate to high risk of bias. The average dose of glucocorticoids (in hydrocortisone equivalents) was 9 to 26.5 ...
CONTEXT: As a result of the introduction of treatment with glucocorticoids and mineralocorticoids, n...
Background: Patients with Congenital Adrenal Hypeplasia (CAH) due to 21-hydroxylase deficiency need...
Congenital adrenal hyperplasia (CAH) caused by 21‐hydroxylase deficiency accountsfor 95% of all CAH ...
OBJECTIVE: Treatment with glucocorticoids and mineralocorticoids has changed congenital adrenal hype...
BACKGROUND: The aim of the study was to evaluate the cardiovascular and metabolic risk profile in pe...
After the introduction of replacement therapy with glucocorticoids and mineralocorticoids in the 195...
After the introduction of replacement therapy with glucocorticoids and mineralocorticoids in the 195...
Background: Congenital adrenal hyperplasia (CAH) is an autosomal recessive disorder caused by impair...
CONTEXT: Congenital adrenal hyperplasia (CAH) is lethal in its most severe forms if not trea...
Objective: There is an increased risk of cardiovascular morbidity in children and adolescents with c...
Increasing evidence indicates that adults with Congenital Adrenal Hyperplasia (CAH) may have a clust...
Treatment with glucocorticoids and mineralocorticoids has changed congenital adrenal hyperplasia (CA...
Context: Patients with classic congenital adrenal hyperplasia (CAH) are treated with lifelong glucoc...
Objective The prevalence of cardiovascular risk factors in congenital adrenal hyperplasia (CAH) vari...
Increasing evidence indicates that adults with Congenital Adrenal Hyperplasia (CAH) may have a clust...
CONTEXT: As a result of the introduction of treatment with glucocorticoids and mineralocorticoids, n...
Background: Patients with Congenital Adrenal Hypeplasia (CAH) due to 21-hydroxylase deficiency need...
Congenital adrenal hyperplasia (CAH) caused by 21‐hydroxylase deficiency accountsfor 95% of all CAH ...
OBJECTIVE: Treatment with glucocorticoids and mineralocorticoids has changed congenital adrenal hype...
BACKGROUND: The aim of the study was to evaluate the cardiovascular and metabolic risk profile in pe...
After the introduction of replacement therapy with glucocorticoids and mineralocorticoids in the 195...
After the introduction of replacement therapy with glucocorticoids and mineralocorticoids in the 195...
Background: Congenital adrenal hyperplasia (CAH) is an autosomal recessive disorder caused by impair...
CONTEXT: Congenital adrenal hyperplasia (CAH) is lethal in its most severe forms if not trea...
Objective: There is an increased risk of cardiovascular morbidity in children and adolescents with c...
Increasing evidence indicates that adults with Congenital Adrenal Hyperplasia (CAH) may have a clust...
Treatment with glucocorticoids and mineralocorticoids has changed congenital adrenal hyperplasia (CA...
Context: Patients with classic congenital adrenal hyperplasia (CAH) are treated with lifelong glucoc...
Objective The prevalence of cardiovascular risk factors in congenital adrenal hyperplasia (CAH) vari...
Increasing evidence indicates that adults with Congenital Adrenal Hyperplasia (CAH) may have a clust...
CONTEXT: As a result of the introduction of treatment with glucocorticoids and mineralocorticoids, n...
Background: Patients with Congenital Adrenal Hypeplasia (CAH) due to 21-hydroxylase deficiency need...
Congenital adrenal hyperplasia (CAH) caused by 21‐hydroxylase deficiency accountsfor 95% of all CAH ...