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1.
Biol Psychiatry Glob Open Sci ; 3(4): 847-854, 2023 Oct.
Article in English | MEDLINE | ID: mdl-37881542

ABSTRACT

Background: Adversity has been linked to accelerated maturation. Molar eruption is a simple and scalable way to identify early maturation, but its developmental correlates remain unexplored. Thus, we examined whether accelerated maturation as indexed by molar eruption is associated with children's mental health or cognitive skills. Methods: Molar eruption was evaluated from T2-weighted magnetic resonance imaging in 117 children (63 female; ages 4-7 years). Parents reported on child mental health with the Child Behavior Checklist. Children completed standardized assessments of fluid reasoning, working memory, processing speed, crystallized knowledge, and math performance. Relationships between molar eruption and developmental outcomes were examined using linear models, with age, gender, and stress risk as covariates. Results: Earlier molar eruption was positively associated with children's externalizing symptoms (false discovery rate-corrected p [pFDR] = .027) but not internalizing symptoms, and the relationship with externalizing symptoms did not hold when controlling for stress risk. Earlier molar eruption was negatively associated with fluid reasoning (pFDR < .001), working memory (pFDR = .033), and crystallized knowledge (pFDR = .001). The association between molar eruption and both reasoning and crystallized knowledge held when controlling for stress risk. Molar eruption also partially mediated associations between stress risk and both reasoning (proportion mediated = 0.273, p = .004) and crystallized knowledge (proportion mediated = 0.126, p = .016). Conclusions: Accelerated maturation, as reflected in early molar eruption, may have consequences for cognitive development, perhaps because it constrains brain plasticity. Knowing the pace of a child's maturation may provide insight into the impact of a child's stress history on their cognitive development.

2.
Proc Natl Acad Sci U S A ; 118(24)2021 06 15.
Article in English | MEDLINE | ID: mdl-34103399

ABSTRACT

Exposure to adversity can accelerate biological aging. However, existing biomarkers of early aging are either costly and difficult to collect, like epigenetic signatures, or cannot be detected until late childhood, like pubertal onset. We evaluated the hypothesis that early adversity is associated with earlier molar eruption, an easily assessed measure that has been used to track the length of childhood across primates. In a preregistered analysis (n = 117, ages 4 to 7 y), we demonstrate that lower family income and exposure to adverse childhood experiences (ACEs) are significantly associated with earlier eruption of the first permanent molars, as rated in T2-weighted magnetic resonance images (MRI). We replicate relationships between income and molar eruption in a population-representative dataset (National Health and Nutrition Examination Survey; n = 1,973). These findings suggest that the impact of stress on the pace of biological development is evident in early childhood, and detectable in the timing of molar eruption.


Subject(s)
Adverse Childhood Experiences , Molar/growth & development , Child , Child, Preschool , Female , Humans , Income , Magnetic Resonance Imaging , Male , Molar/diagnostic imaging , Tooth Eruption
3.
Breast Cancer (Auckl) ; 14: 1178223420924634, 2020.
Article in English | MEDLINE | ID: mdl-32636633

ABSTRACT

A novel melatonin, estrogen, and progesterone hormone therapy was developed as a safe bio-identical alternative hormone therapy for menopausal women based on the Women's Health Initiative findings that PremPro™ increased breast cancer risk and mortality of all types of breast cancer in postmenopausal women. For HER2 breast cancer, melatonin, estrogen, and progesterone delayed tumor onset and reduced tumor incidence in neu female mice. For other breast cancers, its actions are unknown. In this study, melatonin, estrogen, and progesterone hormone therapy were assessed in human ER+ (MCF-7) and triple negative breast cancer (MDA-MB-231) cells, and found to decrease proliferation and migration of both breast cancer lines. Inhibition of MEK1/2 and 5 using PD98059 and BIX02189, respectively, inhibited proliferation and migration in MDA-MB-231 cells and proliferation in MCF-7 cells; however, when combined with melatonin, estrogen, and progesterone, BIX02189 blocked melatonin, estrogen, and progesterone-mediated inhibition of migration in MCF-7 cells and induced Elf-5. For MDA-MB-231 cells, BIX02189 combined with melatonin, estrogen, and progesterone inhibited proliferation and increased pERK1/2 and ß1-INTEGRIN; levels of pERK5 remained low/nearly absent in both breast cancer lines. These findings demonstrate novel anti-cancer actions of melatonin, estrogen, and progesterone in ER+ and triple negative breast cancer cells through intricate MEK1/2- and MEK5-associated signaling cascades that favor anti-proliferation and anti-migration.

4.
Rev. colomb. obstet. ginecol ; 36(3): 156-159, maio-jun. 1985. tab
Article in Spanish | LILACS | ID: lil-1394

ABSTRACT

En un estudio llevado a cabo en el Centro Médico Carmen de la Legua, en Lima, Perú, se compararon los dispositivos T 200 de Cobre y Asa D de Lippes, colocados a mujeres en el período de intervalo. Los dispositivos se distribuyeron al azar y se insertaron con insertadores estándar. La actuación de los dos dispositivos fue similar. Sin embargo, se observó una diferencia estadísticamente significativa (p <0.02) en cuanto a la presencia de inflamaciones pélvicas asociadas al uso de los dispositivos, en los dos grupos. Se produjeron seis casos de inflamaciones pélvicas en el grupo que usó la T 200 de Cobre, mientras que no se observó ningún caso en el grupo que usó el Asa D de Lippes. Se confirmaron tres embarazos en el grupo que usó el Asa D Lippes. Las tasas de continuación a los seis meses, fueron de 96.6 para las mujeres que estaban usando el T de Cobre y 91,4 para las que estaban usando el Asa D de Lippes


Subject(s)
Humans , Female , Intrauterine Devices , Intrauterine Devices, Copper
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