Congenital hypothyroidism: current perspectives

被引:9
作者
Dayal, Devi [1 ]
Prasad, Rajendra [1 ]
机构
[1] Postgrad Inst Med Educ & Res, Dept Pediat, Pediat Endocrinol & Diabet Unit, Chandigarh, India
关键词
congenital hypothyroidism; newborn screening; thyroid stimulating hormone; Down syndrome; IQ; mutations;
D O I
10.2147/RRED.S56402
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Congenital hypothyroidism (CH), the most common pediatric endocrine disorder with an estimated prevalence of 1: 2,000 to 1: 4,000, is an under-recognized problem in countries without routine newborn screening (NBS) programs. Thyroid dysgenesis (TD) is the most common cause of primary CH accounting for approximately 85% of all cases; most of the remaining patients have dyshormonogenesis. Transient CH and CH with eutopic gland, are increasingly being identified after introduction of routine NBS. The clinical features of CH are often subtle resulting in delayed diagnosis and eventually poor intellectual outcome. In developed countries, detection by NBS and early initiation of treatment has largely eliminated the intellectual disability caused by this disorder. The lower screening thyroid stimulating hormone (TSH) cutoff and changes in birth demographics in some countries have been associated with an increase in the reported incidence of CH. However, the additional cases detected by the lower TSH cutoff tend to have either milder or transient hypothyroidism. Diagnosis of CH is made on the basis of serum concentrations of TSH and thyroxine (T4). Thyroid ultrasound, radionuclide scintigraphy, serum thyroglobulin (TG) levels and specific genetic tests help ascertaining the exact etiological diagnosis. Non-availability of later tests should not deter the pediatrician from initiation of treatment. Age at initiation of treatment and starting dose of levothyroxine are critical factors that determine the long-term outcome. Higher doses of levothyroxine at 10-15 mu g/kg/day are required in infants, with titration based on T4 and TSH levels, which are repeated frequently. Coexistence of other congenital anomalies in children with CH adds to the morbidity. Approximately 70% of babies worldwide are not born in an area with an established NBS program and hence are not detected and treated early. Consequently, the economic burden of mental retardation due to CH remains a significant public health challenge in countries without NBS. The health burden owing to CH continues to be high even in countries with well-developed NBS.
引用
收藏
页码:91 / 102
页数:12
相关论文
共 50 条
  • [21] Newborn screening for congenital hypothyroidism in Henan province, China
    Zhao, De-Hua
    Shen, Yong
    Gong, Jiao-Mei
    Meng, Yun
    Su, Li
    Zhang, Xia
    CLINICA CHIMICA ACTA, 2016, 452 : 58 - 60
  • [22] SCREENING FOR CONGENITAL HYPOTHYROIDISM IN TURKEY
    YORDAM, N
    CALIKOGLU, AS
    HATUN, S
    KANDEMIR, N
    OGUZ, H
    TEZIC, T
    OZALP, I
    EUROPEAN JOURNAL OF PEDIATRICS, 1995, 154 (08) : 614 - 616
  • [23] Fifty years of newborn screening for congenital hypothyroidism: current status in Australasia and the case for harmonisation
    Huynh, Tony
    Greaves, Ronda
    Mawad, Nazha
    Greed, Lawrence
    Wotton, Tiffany
    Wiley, Veronica
    Ranieri, Enzo
    Rankin, Wayne
    Ungerer, Jacobus
    Price, Ricky
    Webster, Dianne
    Heather, Natasha
    CLINICAL CHEMISTRY AND LABORATORY MEDICINE, 2022, 60 (10) : 1551 - 1561
  • [24] Genetics of Primary Congenital Hypothyroidism
    Zwaveling-Soonawala, Nitash
    van Trotsenburg, Paul
    PEDIATRIC ENDOCRINOLOGY REVIEWS PER, 2018, 15 (03) : 200 - 215
  • [25] Congenital hypothyroidism: recent advances
    Wassner, Ari J.
    Brown, Rosalind S.
    CURRENT OPINION IN ENDOCRINOLOGY DIABETES AND OBESITY, 2015, 22 (05) : 407 - 412
  • [26] Newborn Screening for Congenital Hypothyroidism and Congenital Adrenal Hyperplasia
    Christopher, Rita
    Devi, A. Radha Rama
    Kabra, Madhulika
    Kapoor, Seema
    Mathur, Roli
    Muranjan, Mamta
    Nigam, Puneet K.
    Pandey, R. M.
    Singh, Arun
    Suresh, S.
    INDIAN JOURNAL OF PEDIATRICS, 2018, 85 (11) : 935 - 940
  • [27] Newborn Screening for Congenital Hypothyroidism and Congenital Adrenal Hyperplasia
    The Indian Journal of Pediatrics, 2018, 85 : 935 - 940
  • [28] Congenital hypothyroidism
    Rodrigues, Ana Luisa
    Carvalho, Ana
    Duarte, Carlos Pereira
    Cesar, Rui
    Anselmo, Joao
    REVISTA PORTUGUESA DE ENDOCRINOLOGIA DIABETES E METABOLISMO, 2014, 9 (01) : 41 - 52
  • [29] Congenital hypothyroidism
    Jain, Vandana
    Agarwal, Ramesh
    Deorari, Ashok K.
    Paul, Vinod K.
    INDIAN JOURNAL OF PEDIATRICS, 2008, 75 (04) : 363 - 367
  • [30] Congenital hypothyroidism
    Carranza, D.
    Van Vliet, G.
    Polak, M.
    ANNALES D ENDOCRINOLOGIE, 2006, 67 (04) : 295 - 302