Predictive Factors of Transient Congenital Hypothyroidism among Filipino Children: A Retrospective Study

Authors

  • Lorna R. Abad, MD Division of Pediatric Endocrinology and Metabolism, Department of Pediatrics, Philippine General Hospital, University of the Philippines Manila
  • Ebner Bon G. Maceda, MD Division of Clinical and Metabolic Genetics, Department of Pediatrics, Philippine General Hospital, University of the Philippines Manila; Institute of Human Genetics, National Institutes of Health, University of the Philippines Manila https://orcid.org/0000-0001-5414-7030
  • Angela Marie D. Leyco, MD Division of Pediatric Endocrinology and Metabolism, Department of Pediatrics, Philippine General Hospital, University of the Philippines Manila
  • Sylvia C. Estrada, MD Division of Pediatric Endocrinology and Metabolism, Department of Pediatrics, Philippine General Hospital, University of the Philippines Manila; Institute of Human Genetics, National Institutes of Health, University of the Philippines Manila

DOI:

https://doi.org/10.47895/amp.vi0.11965

Keywords:

congenital hypothyroidism, Philippines, neonatal screening, prevalence

Abstract

Background and Objective. Transient congenital hypothyroidism (TCH) refers to temporary deficiency of thyroid hormone identified after birth which later recovers to improved thyroxine production. Its prevalence in the Philippines has not been reported in a large-scale study. Its diagnosis remains difficult due to its numerous possible etiologies. Identifying the predictive factors of TCH may aid in earlier diagnosis and decreased risk of overtreatment. This study aimed to determine the predictive factors for TCH in children with congenital hypothyroidism (CH) detected by newborn screening (NBS) in the Philippines from January 2010 to December 2017.

Methods. In this multicenter retrospective cohort study involving 15 NBS continuity clinics in the Philippines, medical records were reviewed, and clinical and laboratory factors were compared between children with TCH and those with permanent congenital hypothyroidism (PCH). Of the 2,913 children diagnosed with CH in the Philippines from 2010 to 2017, 1,163 (39.92%) were excluded from the study due to an unrecalled or lost to follow-up status, or a concomitant diagnosis of Down Syndrome.

Results. Among the 1,750 patients included in analysis, 6.97% were diagnosed with TCH, 60.80% were female, mean gestational age at birth was 38 weeks, and mean birth weight was 2,841 grams. Confirmatory thyrotropin (TSH) was lower and confirmatory free thyroxine (FT4) was higher in the TCH group compared to those with PCH (TSH 32.80 vs 86.65 µIU/mL [p <0.0001]; FT4 9.90 vs 7.37 pmol/L [p 0.001]). The TCH group required lower L-thyroxine doses compared to the PCH group at treatment initiation and at 1, 2, and 3 years of age (initial 6.98 vs 12.08 µg/ kg/day [p <0.0001]; at 1 year 1.89 vs 4.11 µg/kg/day [p <0.0001]; at 2 years 1.21 vs 3.72 µg/kg/day [p <0.0001]; at 3 years 0.83 vs 3.45 µg/kg/day [p <0.0001]). Among those with TCH, mean serum TSH decreased significantly after treatment with L-thyroxine (32.80 vs. 6.55 µIU/ mL, p 0.0001). Other factors associated with TCH were results of thyroid ultrasonography (p 0.007), gestational age at birth (p 0.02), and maternal history of thyroid illness (p <0.0001).

Conclusion. Of all the patients with confirmed congenital hypothyroidism via the newborn screening, 6.97% were diagnosed with transient CH. Factors associated with TCH are confirmatory TSH and FT4, L-thyroxine dose requirements, thyroid ultrasound findings, gestational age at birth, and a maternal history of thyroid illness.

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Published

2025-02-20

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How to Cite

1.
Predictive Factors of Transient Congenital Hypothyroidism among Filipino Children: A Retrospective Study. Acta Med Philipp [Internet]. 2025 Feb. 20 [cited 2025 Apr. 4];. Available from: https://actamedicaphilippina.upm.edu.ph/index.php/acta/article/view/11965

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