Available in Brazil
Molar-incisor hypomineralization (MIH) is characterized by a marked opacity,
asymmetrically involving the first permanent molars and incisors. In more severe cases of
MIH, in addition to the retention of matrix proteins that should have been removed during
the enamel maturation process, its more porous structure allows the penetration of
proteins present in saliva, which bind to the poorly developed hydroxyapatite crystals.
The high protein content of enamel with MIH also promotes the growth of proteolytic
bacteria, posing a challenge for the adhesion of restorative materials and treatments for
hypersensitivity. Some products containing casein phosphopeptide-amorphous calcium
phosphate fluoride (CPP-ACPF) have been used in children with MIH, it can stabilize
calcium, phosphate, and fluoride ions on the tooth surface. Given that MIH lesions have a
high protein content that may prevent the mineralizing agent from reaching the
underdeveloped enamel prisms, it is expected that treatment with CPP-ACPF will be more
effective following prior deproteinization of the affected enamel. A double-blind,
split-mouth, randomized clinical trial will be conducted. The teeth included in the study
will be permanent upper or lower molars with MIH in children aged 7 to 9 years. Two
properly calibrated examiners will select the participants, and the diagnosis of MIH
lesions will be based on the criteria of the European Association of Paediatric Dentistry
(EAPD). The inclusion criteria will be: one permanent molar without MIH; at least two
permanent molars with mild MIH lesions (demarcated opacities without structural loss),
with or without sensitivity, of a cream-white or yellowish color, and 2 mm in diameter;
and without visible bacterial biofilm. The selected teeth from each participant will be
divided into 3 groups: Control Group (molars without hypomineralization); CPP-ACPF Group
(hypomineralized molars treated with CPP-ACPF); and NaOCl/CPP-ACPF Group (hypomineralized
molars deproteinized with 5.25% NaOCl, with application time based on laboratory study
findings, and treated with CPP-ACPF). The randomization of treatments for hypomineralized
teeth will be performed at the time of treatment. The following data collection tools
will be used: a questionnaire to collect demographic and socioeconomic information, as
well as information on etiological factors for HMI; clinical examination to assess the
following aspects of the lesions: location (occlusal or middle third), lesion area (in
mm²), color (cream-white or yellowish), visual appearance (shiny or opaque), sensitivity,
and lightness of the lesion color (L). The tooth's L will be measured three times to
obtain the average of the values. The data will be analyzed descriptively and
inferentially. Clinical analyses will include intragroup comparisons (between follow-up
times) and intergroup comparisons (between group outcomes), at a 5% significance level.
1Research sites
54Patients around the world