Congenital hypothyroidism screening program in iran; a systematic review and metaanalysis

Yousef Veisani1, Kourosh Sayehmiri2, Shahab Rezaeian3

  • 1Student Research Committee.

Insights

Newborn screening for congenital hypothyroidism (CH) in Iran identified an incidence of 2/1000 neonates. Further research is needed to optimize TSH cut-off levels for accurate recall rates.

Area of Science:

  • Neonatal screening
  • Endocrinology
  • Public health

Background:

  • Congenital hypothyroidism (CH) can cause intellectual disability if not treated promptly.
  • Early detection through newborn screening and timely thyroid hormone replacement is crucial for normal cognitive development.

Purpose of the Study:

  • To systematically review and evaluate the national CH screening program results across Iranian provinces.
  • To assess the incidence and recall rates of CH in Iran.

Main Methods:

  • A systematic literature review of national and international databases (PubMed, Scopus, Web of Science, etc.).
  • Meta-analysis of 25 studies involving 1,425,124 neonates using random-effects models.
  • Exploration of heterogeneity using meta-regression.

Main Results:

  • The pooled recall rate for TSH ≥5mIU/L was 0.014 (95% CI: 0.013-0.015).
  • The overall incidence of CH was determined to be 2 per 1000 neonates (95% CI: 0.002-0.002).
  • No significant increase in CH incidence over time was observed (P=0.08).

Conclusions:

  • The current TSH cut-off of ≥5mIU/L for recalling neonates has a low positive predictive value (14%).
  • Further research is required to establish more accurate TSH thresholds for neonatal recall.
  • Optimizing screening criteria can improve the efficiency and accuracy of CH detection programs.
Abstract

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