# Prevalence and associated factors of molar incisor hypomineralization in children: a cross-sectional study

**Authors:** Selin Sena Yılmaz, İlhan Uzel, Fahinur Ertuğrul, Şule Gökçe, Emine Burçe Dörtkardeşler, Güneş Ak

PMC · DOI: 10.1186/s12903-025-07071-2 · 2025-11-25

## TL;DR

This study finds that a dental condition called MIH in children is linked to factors like socioeconomic status, antibiotic use, and breastfeeding duration.

## Contribution

The study identifies new associations between MIH and factors such as maternal employment, birth weight, and exclusive breastfeeding.

## Key findings

- MIH prevalence was 12% with 76% of cases showing severe defects.
- Exclusive breastfeeding duration was longer in children without MIH.
- Risk factors included socioeconomic status, antibiotic use, and respiratory infections.

## Abstract

Molar Incisor Hypomineralization (MIH) is a qualitative enamel defect affecting first permanent molars often involving incisors. It presents clinical challenges including hypersensitivity, rapid caries, and restorative difficulties. Though its etiology is unclear, systemic and environmental factors have been implicated.

This study aimed to determine the prevalence and associated factors of MIH and to assess the risk factors.

A cross-sectional study was conducted on children aged 6–12 years in İzmir, Türkiye. Among 700 children examined, 50 diagnosed with MIH were included in the case group, while 50 healthy children formed the control group. Parental interviews assessed sociodemographic, prenatal, perinatal, postnatal factor. Biochemical parameters were analyzed appropriate statistical tests.

MIH prevalence was 12% and 76% had severe defects (MIH-2), and 24% had mild opacities (MIH-1). Significant associations were observed with socioeconomic status, maternal employment, birth weight, antibiotic use and respiratory infections (p < 0.005). Exclusive breastfeeding duration was longer in controls (p = 0.020).

MIH is a multifactorial condition influenced by systemic and environmental factors. Early diagnosis and prevention are essential. Longer breastfeeding duration may offer a protective effect. Larger longitudinal studies are needed to better understand associated factor of MIH.

The online version contains supplementary material available at 10.1186/s12903-025-07071-2.

## Full-text entities

- **Genes:** IGHE (immunoglobulin heavy constant epsilon) [NCBI Gene 3497] {aka IgE}, PTH (parathyroid hormone) [NCBI Gene 5741] {aka FIH1, PTH1}, CASP4 (caspase 4) [NCBI Gene 837] {aka CASP-4, ICE(rel)II, ICEREL-II, ICH-2, Mih1, Mih1/TX}, ALPP (alkaline phosphatase, placental) [NCBI Gene 250] {aka ALP, PALP, PLAP, PLAP-1}, TGFBR1 (transforming growth factor beta receptor 1) [NCBI Gene 7046] {aka AAT5, ACVRLK4, ALK-5, ALK5, ESS1, LDS1}
- **Diseases:** fever (MESH:D005334), chronic kidney disease (MESH:D051436), masticatory dysfunction (MESH:C563600), chronic renal failure (MESH:D007676), Prematurity (MESH:C536271), pharyngitis (MESH:D010612), chickenpox (MESH:D002644), otitis (MESH:D010031), allergic (MESH:D004342), enamel hypoplasia (MESH:D003744), tonsillitis (MESH:D014069), pneumonia (MESH:D011014), MIH (MESH:D000094604), scarlet fever (MESH:D012541), diarrhea (MESH:D003967), inflammatory (MESH:D007249), bone marrow inflammation (MESH:D010000), metabolic disorders (MESH:D008659), gastroenteritis hand and foot mouth disease (MESH:D006232), intellectual disability (MESH:D008607), systemic diseases (MESH:D034721), cardiac disease (MESH:D006331), vitamin and mineral deficiencies (MESH:C537337), allergic rhinitis (MESH:D065631), atopic dermatitis (MESH:D003876), premature birth (MESH:D047928), gastrointestinal disorders (MESH:D005767), Urine Tract Infection (MESH:D012141), Respiratory diseases (MESH:D012140), monocytosis (MESH:C538328), rubella (MESH:D012409), diseases (MESH:D004194), AGE (OMIM:613784), malnourished (MESH:D044342), food allergies (MESH:D005512), amelogenesis imperfecta (MESH:D000567), trauma (MESH:D014947), bronchitis (MESH:D001991), vitamin D deficiency (MESH:D014808), sepsis (MESH:D018805), urinary infections (MESH:D014552), Intellectuel Disability (MESH:D009069), ID (MESH:C537985), Acute Gastroenteritis (MESH:D005759), febrile conditions (MESH:D020763), measles (MESH:D008457), developmental enamel defects (MESH:D000094602), dental anomalies (OMIM:614188), asthma (MESH:D001249), otitis media (MESH:D010033), caries (MESH:D003731), TIBC (MESH:D000090463), atopic (MESH:C566404), atopic diseases (MESH:D006969), infection (MESH:D007239), obese (MESH:D009765), dermatitis (MESH:D003872), neonatal jaundice (MESH:D007567), digestive system diseases (MESH:D004066), underweight (MESH:D013851)
- **Chemicals:** vitamin D (MESH:D014807), urea (MESH:D014508), creatinine (MESH:D003404), Iron (MESH:D007501), phosphorus (MESH:D010758), calcium (MESH:D002118), Vitamin B12 (MESH:D014805), fluoride (MESH:D005459)
- **Species:** Homo sapiens (human, species) [taxon 9606], Meleagris gallopavo (common turkey, species) [taxon 9103], Canis lupus familiaris (dog, subspecies) [taxon 9615]
- **Cell lines:** MIH-2 — Homo sapiens (Human), Colon carcinoma, Cancer cell line (CVCL_A628)

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12648818/full.md

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Source: https://tomesphere.com/paper/PMC12648818