Increased Cardiovascular and Metabolic Morbidity in Patients With 21-Hydroxylase Deficiency: A Swedish Population-Based National Cohort Study

• Published in: The journal of clinical endocrinology and metabolism 2015-09, Vol.100 (9), p.3520-3528
• Main Authors: Falhammar, Henrik, Frisén, Louise, Hirschberg, Angelica Linden, Norrby, Christina, Almqvist, Catarina, Nordenskjöld, Agneta, Nordenström, Anna
• Format: Article
• Language: English
• Subjects: Adolescent; Adrenal Hyperplasia, Congenital - epidemiology; Adrenal Hyperplasia, Congenital - genetics; Adult; Aged; Aged, 80 and over; Cardiovascular Diseases - epidemiology; Cardiovascular Diseases - genetics; Child; Child, Preschool; Cohort Studies; Female; Genotype; Humans; Infant; Infant, Newborn; Male; MEDICAL AND HEALTH SCIENCES; MEDICIN OCH HÄLSOVETENSKAP; Metabolic Diseases - epidemiology; Metabolic Diseases - genetics; Middle Aged; Neonatal Screening; Prevalence; Risk; Steroid 21-Hydroxylase - genetics; Young Adult
• ISSN: 0021-972X; 1945-7197; 1945-7197
• DOI: 10.1210/JC.2015-2093

Context: Congenital adrenal hyperplasia (CAH) is lethal in its most severe forms if not treated with glucocorticoids. However, glucocorticoids may increase the risk of cardiovascular and metabolic morbidity. Objective: This study aimed to study cardiovascular and metabolic morbidity in CAH. Design, Setting, and Participants: Patients with CAH due to 21-hydroxylase deficiency (n = 588; >80% with known CYP21A2 mutations) were compared with controls matched for sex, year, and place of birth (n = 58 800). Data were obtained by linking national population-based registers. Subgroup analyses were performed regarding sex, clinical severity (salt wasting, simple virilizing, nonclassic), CYP21A2 genotype (null, I2 splice, I172N, P30L), and stratified by the introduction of neonatal screening, age groups, and nonobesity. Main Outcome Measures: To study cardiovascular and metabolic morbidity in CAH. Results: In CAH, both any cardiovascular and metabolic disorders (OR [odds ratio], 3.9; 95% CI [confidence interval], 3.1–5.0), and cardiovascular disease (OR, 2.7; 95% CI, 1.9–3.9) were increased. Separate analyses of the individual diseases showed higher frequencies in CAH of hypertension, hyperlipidemia, atrial fibrillation, venous thromboembolism, obesity, diabetes (mainly type 2), obstructive sleep disorder, thyrotoxicosis, and hypothyroidism. Similar results were seen in the stratified groups. On the subgroup level, females were generally more affected (especially I172N and the nonclassic group), as were males with the null genotype. Conclusions: CAH was associated with excess cardiovascular and metabolic morbidity but the mechanism is not certain as the glucocorticoids were not assessed. Hypothyroidism and obesity may be an effect of close observation. However, more severe conditions were presumably detected equally in patients and controls. Screening for diabetes and other metabolic disorders that increase cardiovascular risk is important.