Correlation Between Congenital Hypothyroidism and Hearing Loss in Newborn

Authors

  • Watcharapol Poonual Department of Otolaryngology, Uttaradit Hospital, Uttaradit, Thailand

Keywords:

Correlation, Congenital hypothyroidism, Hearing loss, Newborn

Abstract

Introduction: Congenital hypothyroidism increases the risk of hearing loss which caused delay speech and language development, social and emotional problems, and educational failure. Currently, a universal hearing screening program in newborns has been implemented in Thailand. The congenital hypothyroidism is not considered as a risk factor for hearing loss resulting in restricted hospitals that do not be screening hearing loss among congenital hypothyroidism. Then this research is to study the correlation between congenital hypo-thyroidism and hearing loss in a newborn in Uttaradit hospital, Thailand.
Methods: A retrospective cohort study of 382 newborns in Uttaradit hospital between January 2011 to June 2020 was obtained from medical records, Thyroid-stimulating hormone (TSH) screening report in newborn, the evaluation of otoacoustic emission (OAE) and auditory brainstem response (ABR), divided into 2 groups, 62 patients were congenital hypothyroidism (exposed group) and 320 patients were non-congenital hypothyroidism (non-exposed group). Data were analyzed by using descriptive statistics and analytical statistics by a computer program.
Results: Newborn with congenital hypothyroidism was 2.5 times significantly greater risk of hearing loss (95% CI 1.27 - 4.95, P = .008).
Conclusions: Congenital hypothyroidism affected hearing loss in newborns. Therefore, early screening should be necessary for newborns to reduce the risk of hearing loss and also improve the quality of life

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References

Hafsa M, Sibtain A, Imran S, Khadija H, Hussain K, Aysha K. Newborn screening for congenital hypothyroidism: improvement in short-term follow-up by audit and monitoring. BMC Res Notes. 2020;13(563):2-6.

Zhu Y, Bing D, Wang D, et al. Analysis of thyroid dysfunction in patients with sudden sensorineural hearing loss. World J Otorhinolaryngol Head Neck Surg. 2020;7(1):1-8. doi: 10.1016/j.wjorl.2019.02.002.

Melse-Boonstra A, Mackenzie I. Iodine deficiency, thyroid function and hearing deficit: a review. Nutr Res Rev. 2013;26(2):110-117.

Andrade C, Lemos A, Machado G, et al. Congenital Hypothyroidism as a risk factor for Central Hearing Process Disorders. Rev Paul Pediatr. 2019;37(1):82-89.

Saffari F, Nikpendar MH, Esmailzadehha N, Oveisi S, Homaei A, Jalilolghadr S. Prevalence of Sensorineural Hearing Loss in Patients with Congenital Hypothyroidism in Qazvin. Iranian Journal of Neonatology. 2018;9(3):1-5.

Titirungruang C, Charusripan P, Patarapak S. Early detection of infant hearing impairment. Chula Med J. 2018;62(1):53-65.

Rovet J, Walker W, Bliss B, Buchanan L, Ehrlich R. Long-term sequelae of hearing impairment in congenital hypothyroidism. J Pediatr. 1996;128(6):776-783. doi: 10.1016/s0022-3476(96)70329-3.

Poonual W, Navacharoen N, Kangsanarak J, Namwongprom S, Saokaew S. Hearing loss screening tool (COBRA score) for newborns in primary care setting. Korean J Pediatr. 2017;60(11):353-358. doi: 10.3345/kjp.2017.60.11.353.

Ngamsanga S. Cost-effectiveness analysis of newborn hearing screening program. Chula Med Bull. 2019;1(6):555-561.

Francois M, Bonfils P, Leger J, Czernichow P, Narcy P. Role of congenital hypothyroidism in hearing loss in children. J Pediatr. 1994;124(3):444-446.

Hashemipour M, Hovsepian S, Hashemi M, Amini M, Kelishadi R, Sadeghi S. Hearing impairment in congenitally hypothyroid patients. Iran J Pediatr. 2012;22(1):92-96.

Dayal D, Hansdak N, Vir D, Gupta A, Bakshi J. Hearing impairment in children with permanent congenital hypothyroidism: Data from Northwest India. Thyroid Res Pract. 2016;13:67-70.

Jiang M, Karasawa T, Steyger TS. Aminoglycoside-induced cochleotoxicity, a review. Frontiers in cellular neuroscience. 2017;11:308.

Petersen L, Rogers C. Aminoglycoside-induced hearing deficits - a review of cochlear ototoxicity. South African Family Practice. 2015;57(2):77-82.

Poonual W, Navacharoen N, Kangsanarak J, Namwongprom S. Risk factors for hearing loss in infants under universal hearing screening program in Northern Thailand. J Multidiscip Healthc. 2015;9:1-5. doi: 10.2147/JMDH.S92818.

Vohr B, Widen J, Cone-Wesson B, et al. Identification of neonatal hearing impairment: characteristics of infants in the neonatal intensive care unit and well-baby nursery. Ear Hear. 2000;21(5):373-382. doi: 10.1097/00003446-200010000-00005.

Emmanouil N, Vasilios C, Pavlos M, Antonios T, Thomas N, Cone-Wesson B. Risk factors affecting hearing in neonatal intensive care unit neonates. J Hear Sci. 2016;6(3):45-53.

Gamboa I, Carneiro de Sousa P, Duarte D, Oliveira N. Amikacin Ototoxicity: Case Report and Literature Review. Journal of Otolaryngology. 2018;8(4):180.

Cross C, Liao S, Urdang Z, Srikanth P, Garinis A, Steyger P. Effect of sepsis and systemic inflammatory response syndrome on neonatal earing screening outcomes following gentamicin exposure. Int J Pediatr Otorhinolaryngol. 2015;79(11):1915-1919. doi: 10.1016/j.ijporl.2015.09.004.

Fischer N, Mathonia N, Hoellerich G, et al. Surviving murine experimental sepsis affects the function and morphology of the inner ear. Biol Open. 2017;6(6):732-740. doi: 10.1242/bio.024588.

Thangavelu K, Martakis K, Fabian S, et al. Prevalence and risk factors for hearing loss in high-risk neonates in Germany. Acta Paediatr. 2019;108(11):1972-1977. doi: 10.1111/apa.14837.

Mustapha M, Fang Q, Gong T, et al. Deafness and permanently reduced potassium channel gene expression and function in hypothyroid Pit1dw mutants. J Neurosci. 2009;29(4):1212-1223. doi: 10.1523/JNEUROSCI.4957-08.2009.

Fang Q, Giordimaina AM, Dolan DF, Camper SA, Mustapha M. Genetic Background of Prop1df Mutants Provides Remarkable Protection Against Hypothyroidism-Induced Hearing Impairment. JARO. 2012;13:173-184.

Inglesby D, Sluder C, Liu Y, Nguyen S, Meyer T. Hearing Loss Severity and Progression in Children with Congenital Hypothyroidism. Journal of Pedriatric Endocrinology. 2019;4(1):1030.

Di Lorenzo L, Foggia L, Panza N, et al. Auditory brainstem responses in thyroid diseases before and after therapy. Horm Res. 1995;43(5):200-205. doi: 10.1159/000184278.

Karakus CF, Altuntas EE, Kilicli F, Durmus K, Hasbek Z. Is sensorineural hearing loss related with thyroid metabolism disorders. Indian Journal of Otology. 2015;21(2):138-143.

Hussein MM, Asal SI, Salem TM, Mohammed AM. The effect of L-thyroxine hormone therapy on hearing loss in hypothyroid patients. The Egyptian Journal of Otolaryngology. 2017;33:637-644

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Published

2022-04-28

How to Cite

[1]
Poonual, W. 2022. Correlation Between Congenital Hypothyroidism and Hearing Loss in Newborn. Asian Medical Journal and Alternative Medicine. 22, 1 (Apr. 2022), 33–39.

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Section

Original Articles