on Congenital Hypothyroidism and Newborn Screening Program in Africa ; the Present Situation and the Way Forward

Congenital hypothyroidism (CH) is a condition that affects infants from birth (congenital) and results from partial or complete loss of thyroid function (hypothyroidism). CH has existed since antiquity, as exemplified by goitrous dwarfs in 400 BC in South America, writing about goiter from ancient Rome in the first century and descriptions of mental retardation and goitrous hypothyroidism in a lecture and subsequent publication by Paracelsus in the sixteenth century [1]. Non goitrous sporadic CH was not described until the beginning of the industrial revolution by Thomas Curling in 1850. By the end of the nineteenth century, thyroid extract were observed to effectively treat patients with CH, however not until the 1970s was it possible for mental retardation caused by CH to be virtually eradicated by early treatment as a result of early diagnosis through newborn screening [2]. During the second half of the twentieth century, various enzymatic defects in hormonogenesis were shown to be responsible for CH [3]. Immune mediated mechanism have also been proposed to cause thyroid dysgenesis, but a causal relationship has not been proven [4,5]. In the 1990s mutations in the extracellular domain of Thyrotropin (TSH) receptor in the ß sub unit of TSH and the transcription factors that regulate thyroid embryogenesis have been found to be rare cause of CH [6-10]. The suffering and heavy social and economic burden caused by congenital hypothyroidism prompted many countries to institute a formalized screening programme directed at newborns, just as a vaccination programme has become an integral part of child health care. In African countries however, this type of formalized service has not yet been established. Yet most African countries have crude birth rates (Nigeria-39.9, Kenya-39.2, south Africa-22.3 and Egypt-24.2) above the average (20.3 births per 1,000population) for the entire world, for African countries, the implementation of a universal neonatal screening programme will bring about a considerable improvement in child health care.

[1]  K. Alimohammadzadeh,et al.  Cost–Benefit and Effectiveness of Newborn Screening of Congenital Hypothyroidism: Findings from a National Program in Iran , 2010 .

[2]  K. Fujieda,et al.  Central Congenital Hypothyroidism Detected by Neonatal Screening in Sapporo, Japan (2000–2004): It’s Prevalence and Clinical Characteristics , 2008, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

[3]  F. Khan,et al.  Resetting the detection level of cord blood thyroid stimulating hormone (TSH) for the diagnosis of congenital hypothyroidism. , 2007, Journal of tropical pediatrics.

[4]  G. Borrajo,et al.  Newborn screening in Latin America at the beginning of the 21st century , 2007, Journal of Inherited Metabolic Disease.

[5]  M. Donaldson,et al.  Improvement in screening performance and diagnosis of congenital hypothyroidism in Scotland 1979–2003 , 2006, Archives of Disease in Childhood.

[6]  Nandita Chatterjee,et al.  Umbilical cord blood TSH levels in term neonates: a screening tool for congenital hypothyroidism. , 2005, Indian pediatrics.

[7]  Rosário Santos,et al.  Mutation screening of the thyroid peroxidase gene in a cohort of 55 Portuguese patients with congenital hypothyroidism. , 2005, European journal of endocrinology.

[8]  M. Polak,et al.  PAX8, TITF1, and FOXE1 gene expression patterns during human development: new insights into human thyroid development and thyroid dysgenesis-associated malformations. , 2005, The Journal of clinical endocrinology and metabolism.

[9]  C. Garel,et al.  Thyroid abnormalities by ultrasonography in neonates with congenital hypothyroidism. , 2003, The Journal of pediatrics.

[10]  Junya Jirapradittha,et al.  Newborn screening for congenital hypothyroidism in Khon Kaen University Hospital, the first three years, a preliminary report. , 2003, Journal of the Medical Association of Thailand = Chotmaihet thangphaet.

[11]  P. Mirmiran,et al.  Screening for congenital hypothyroidism in the Islamic Republic of Iran: strategies, obstacles and future perspectives. , 2002, Eastern Mediterranean health journal = La revue de sante de la Mediterranee orientale = al-Majallah al-sihhiyah li-sharq al-mutawassit.

[12]  S. Costagliola,et al.  Germline mutations of TSH receptor gene as cause of nonautoimmune subclinical hypothyroidism. , 2002, The Journal of clinical endocrinology and metabolism.

[13]  F. Deneke,et al.  Neonatal congenital hypothyroidism screening in Addis Ababa, Ethiopia. , 2000, East African medical journal.

[14]  R. Pfäffle,et al.  Congenital central hypothyroidism due to a homozygous mutation in the thyrotropin beta-subunit gene follows an autosomal recessive inheritance. , 1998, The Journal of clinical endocrinology and metabolism.

[15]  O. Chidede,et al.  Thyroid function in neonates from goitre prevalent areas in Zimbabwe. , 1998, The Central African journal of medicine.

[16]  J. Parma,et al.  Familial congenital hypothyroidism due to inactivating mutation of the thyrotropin receptor causing profound hypoplasia of the thyroid gland. , 1997, The Journal of clinical investigation.

[17]  Wei Wu,et al.  Pituitary lineage determination by the Prophet of Pit-1 homeodomain factor defective in Ames dwarfism , 1996, Nature.

[18]  J. Sack,et al.  IODINE AND HYPOTHYROIDISM IN NEONATES WITH CONGENITAL HEART DISEASE.† 1338 , 1996, Pediatric Research.

[19]  M. Arnone,et al.  Molecular events in the differentiation of the thyroid gland , 1995, Journal of endocrinological investigation.

[20]  Y. Hayashi,et al.  Brief report: resistance to thyrotropin caused by mutations in the thyrotropin-receptor gene. , 1995, The New England journal of medicine.

[21]  Z. Laron Congenital hypoparathyroidism. , 1995, Israel journal of medical sciences.

[22]  G. Delong,et al.  Timing of vulnerability of the brain to iodine deficiency in endemic cretinism. , 1994, The New England journal of medicine.

[23]  H. Hitzeroth Screening for congenital hypothyroidism in South Africa , 1994 .

[24]  U. Isichei,et al.  A comparative study of thyroid function in African neonates: a reference thyroid profile. , 1993, Clinica chimica acta; international journal of clinical chemistry.

[25]  Rosalind S. Brown,et al.  Detection of thyrotropin binding inhibitory activity in neonatal blood spots. , 1993, The Journal of clinical endocrinology and metabolism.

[26]  J. Toublanc Comparison of epidemiological data on congenital hypothyroidism in Europe with those of other parts in the world. , 1992, Hormone research.

[27]  Y. Hayashizaki,et al.  Thyroid‐stimulating hormone (TSH) deficiency caused by a single base substitution in the CAGYC region of the beta‐subunit. , 1989, The EMBO journal.

[28]  A. Grüters,et al.  Cytotoxic antibodies in congenital hypothyroidism. , 1989, The Journal of clinical endocrinology and metabolism.

[29]  R. Bernstein,et al.  Neonatal screening for congenital hypothyroidism. A decade's review, including South Africa. , 1988, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

[30]  R. Ehrlich,et al.  Intellectual outcome in children with fetal hypothyroidism. , 1987, The Journal of pediatrics.

[31]  H. Drexhage,et al.  ROLE OF MATERNAL IMMUNOGLOBULINS BLOCKING TSH-INDUCED THYROID GROWTH IN SPORADIC FORMS OF CONGENITAL HYPOTHYROIDISM , 1985, The Lancet.

[32]  R. Klein Infantile hypothyroidism then and now: the results of neonatal screening. , 1985, Current problems in pediatrics.

[33]  David Ninan,et al.  Thyroid Disorders , 1985, Absolute Obstetric Anesthesia Review.

[34]  K. Ito,et al.  Sequential serum measurements of thyrotropin binding inhibitor immunoglobulin G in transient familial neonatal hypothyroidism. , 1983, The Journal of clinical endocrinology and metabolism.

[35]  D. Finegold,et al.  Transient thyroid suppression associated with topically applied povidone-iodine. , 1982, American journal of diseases of children.

[36]  EFFECTS OF NEONATAL SCREENING FOR HYPOTHYROIDISM: PREVENTION OF MENTAL RETARDATION BY TREATMENT BEFORE CLINICAL MANIFESTATIONS New England Congenital Hypothyroidism Collaborative , 1981, The Lancet.

[37]  J. Konishi,et al.  Familial neonatal transient hypothyroidism due to maternal TSH-binding inhibitor immunoglobulins. , 1980, The New England journal of medicine.

[38]  M. Mitchell,et al.  Screening for congenital hypothyroidism: results of screening one million North American infants. , 1979, The Journal of pediatrics.

[39]  C. Laberge,et al.  Preliminary report on a mass screening program for neonatal hypothyroidism. , 1975, The Journal of pediatrics.

[40]  A. Klein,et al.  Improved prognosis in congenital hypothyroidism treated before age three months. , 1972, The Journal of pediatrics.