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Endocrinol Metab (Seoul). 2022;37(1):138-147.

Epidemiology and Long-Term Adverse Outcomes in Korean Patients with Congenital Adrenal Hyperplasia: A Nationwide Study.

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제1저자 김정희, 최선규 · 교신저자 김신곤

PMID 35255606 PMC8901972 DOI 10.3803/EnM.2021.1328 IF 5.1 내분비대사내과
소속 (4)
  1. Department of Internal Medicine, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.
  2. Department of Biostatistics, Korea University College of Medicine, Seoul, Korea.
  3. Department of Pediatrics, Seoul National University Children's Hospital, Seoul National University College of Medicine, Seoul, Korea.
  4. Division of Endocrinology and Metabolism, Department of Internal Medicine, Korea University College of Medicine, Seoul, Korea.

Abstract

BACKGROUND Previous studies on the epidemiology and complications of congenital adrenal hyperplasia (CAH) were conducted in Western countries and in children/adolescents. We aimed to explore the epidemiology of CAH, as well as the risk of comorbidities and mortality, in a Korean nationwide case-control study.

METHODS CAH patients (n=2,840) were included between 2002 and 2017 from the National Health Insurance Service database and the Rare Intractable Disease program. CAH patients were compared, at a 1:10 ratio, with age-, sex-, and index year-matched controls (n=28,400).

RESULTS The point prevalence of CAH patients in Korea was 1 in 18,745 persons in 2017. The annual incidence rate declined between 2003 and 2017 from 3.25 to 0.41 per 100,000 persons. CAH patients were at elevated risk for cardiovascular disease (odds ratio [OR], 1.6; 95% confidence interval [CI], 1.4 to 1.9), stroke (OR, 1.7; 95% CI, 1.3 to 2.0), diabetes mellitus (OR, 2.8; 95% CI, 2.6 to 3.1), dyslipidemia (OR, 2.4; 95% CI, 2.2 to 2.6), and psychiatric disorders (OR, 1.5; 95% CI, 1.3 to 1.6). Fracture risk increased in CAH patients aged over 40 years (OR, 1.4; 95% CI, 1.1 to 1.7). CAH patients were at higher risk of mortality than controls (hazard ratio, 1.6; 95% CI, 1.3 to 2.0).

CONCLUSION Our nationwide study showed a recent decline in the incidence of CAH and an elevated risk for cardiovascular, metabolic, skeletal, and psychiatric disorders in CAH patients. Lifelong management for comorbidity risk is a crucial component of treating CAH patients.

Keywords

Adrenal hyperplasia, congenitalComorbidityEpidemiologyLong term adverse effectsMortality

Figures

Fig. 1
Fig. 1 Annual incidence and number of patients with congenital adrenal hyperplasia according to age and the index year (2003 to 2017).
Fig. 2
Fig. 2 Annual incidence per 10,000 live births and number of newborns/infants with congenital adrenal hyperplasia according to the index year (2002 to 2017).
Fig. 3
Fig. 3 (A) Glucocorticoid and (B) mineralocorticoid regimens with 6 months or more duration within 1 year before the last visit.
Fig. 4
Fig. 4 Survival probability of congenital adrenal hyperplasia (CAH) patients compared with age- and sex-matched controls. HR, hazard ratio; CI, confidence interval.

그림 출처: PubMed Central 공개 논문 (PMC8901972)

Conflict of interest statement

CONFLICTS OF INTEREST . No potential conflict of interest relevant to this article was reported.

그 밖의 정보
출판 형태
Journal Article, Research Support, Non-U.S. Gov't
저널
Endocrinology and metabolism (Seoul, Korea) · eISSN 2093-5978
전자 출판
2022-02-28
MeSH
Adrenal Hyperplasia, Congenital* / complications / epidemiology / metabolism · Adult · Cardiovascular Diseases* / etiology · Case-Control Studies · Diabetes Mellitus* · Humans · Republic of Korea / epidemiology
참고문헌
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