Publications by authors named "Lynne Levitsky"

Article Synopsis
  • - Myhre syndrome is a rare genetic disorder linked to mutations in the SMAD4 gene, with recent studies from Massachusetts General Hospital highlighting its complexities through evaluations of 47 patients.
  • - The findings indicate that symptom progression occurs in all patients after at least 5 years of observation, with different SMAD4 variants associated with varying health outcomes, particularly regarding hearing loss and aortic hypoplasia.
  • - There is a call for more research and evidence-based guidelines to improve understanding and treatment of Myhre syndrome, especially given the serious complications observed, including deaths related to cardiovascular issues.
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Article Synopsis
  • Youth-onset type 2 diabetes (T2D) shows more severe symptoms and complications compared to adult-onset T2D, prompting researchers to analyze its underlying factors.
  • The study stemmed from the TODAY clinical trial, involving 398 adolescents aged 10 to 17 with T2D, who were monitored over nearly 4 years to assess the impact of growth hormone mediators on their condition.
  • Key outcomes included tracking glycemic control, insulin sensitivity, and beta cell function, with findings indicating a correlation between increasing IGF-1 levels and better management of diabetes in youth.
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  • * A study examined genetic sequences from over 3,000 youth-onset T2D patients, finding specific gene variants and associations related to obesity and diabetes.
  • * The research indicates that youth-onset T2D shares genetic factors with adult-onset T2D but shows a higher prevalence of rare variants, suggesting it is a diverse condition that falls between monogenic diabetes and adult-onset T2D.
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Youth-onset type 2 diabetes (T2D) is a growing public health concern. Its genetic basis and relationship to other forms of diabetes are largely unknown. To gain insight into the genetic architecture and biology of youth-onset T2D, we analyzed exome sequences of 3,005 youth-onset T2D cases and 9,777 ancestry matched adult controls.

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Article Synopsis
  • The study addresses the underrepresentation of the Latino population in genetic research and highlights how existing methods rely on imputation that misses important low-frequency variants.
  • Researchers utilized the NHLBI's TOPMed panel for a more in-depth analysis of rare genetic variations in relation to type 2 diabetes among 8,150 Latino individuals.
  • The findings revealed 26 significant genetic signals, including a new variant, and led to the creation of a Latino-specific polygenic score that improved risk prediction for type 2 diabetes, showcasing the effectiveness of the TOPMed imputation method.
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Objective: To evaluate changes in retinal thickness and morphology using OCT in youth with type 2 diabetes (T2D) and to identify systemic biomarkers correlating with these changes.

Design: Retrospective subgroup analysis of a prospective study.

Participants: Participants who underwent OCT imaging in the Treatment Options for Type 2 Diabetes in Adolescents and Youth (TODAY) trial and its follow-up study TODAY2.

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The past 200 years have brought an understanding of diabetes and its pathogenesis, as well as the development of treatments that could not have been predicted when the disorder was first clinically described 2000 years ago. Beginning in the late 19th century, the initial descriptions of the microscopic anatomy of the pancreatic islets by Langerhans led to recognition of pancreatic endocrine function. Many investigators attempted to isolate the hypoglycemic factor produced by the pancreas, but Banting, Best, Macleod, and Collip were able to extract and purify "isletin" to treat human diabetes in 1921.

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Purpose Of Review: The potential for fertility in Turner syndrome has improved in recent years. Understanding of associated risks and approaches is important for the care of girls and women with this condition. This review focuses on reproductive health, fertility options and appropriate counselling for women with Turner syndrome and their families.

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Aim: To understand the relationship of obesity and 27 circulating inflammatory biomarkers to the prevalence of non-proliferative diabetic retinopathy (NPDR) in youth with type 2 diabetes.

Methods: Youth with type 2 diabetes who participated in the TODAY (Treatment Options for Type 2 Diabetes in Adolescents and Youth) study were followed for 2-6.5 years.

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Objective: Maturity-onset diabetes of the young (MODY) is frequently misdiagnosed as type 1 or type 2 diabetes. Correct diagnosis may result in a change in clinical treatment and impacts prediction of complications and familial risk. In this study, we aimed to assess the prevalence of MODY in multiethnic youth under age 20 years with a clinical diagnosis of type 2 diabetes.

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Article Synopsis
  • - The study aims to explore the relationship between the percentage of 45,X cells and the phenotypic conditions in women with Turner syndrome, particularly focusing on cardiac, renal, and thyroid issues.
  • - Results show that patients with ≤70% 45,X have fewer cardiac and renal anomalies compared to those with >70%, indicating a connection between karyotype and health outcomes.
  • - The findings suggest a need for more extensive research and collaboration to enhance clinical guidelines for Turner syndrome, allowing for more personalized counseling based on the specific genetic makeup of patients.
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Background: Although physical activity (PA) has been shown in helping prevent and treat obesity, current PA interventions are still not effective in ameliorating the obesity epidemic. Additional forms of PA need to be investigated to improve PA engagement and outcomes. We hypothesize that pairing a narrative (i.

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Diabetic ketoacidosis (DKA) is the end result of insulin deficiency in type 1 diabetes mellitus (T1D). Loss of insulin production leads to profound catabolism with increased gluconeogenesis, glycogenolysis, lipolysis, and muscle proteolysis causing hyperglycemia and osmotic diuresis. High levels of counter-regulatory hormones lead to enhanced ketogenesis and the release of 'ketone bodies' into the circulation, which dissociate to release hydrogen ions and cause an overwhelming acidosis.

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Objective: In treatment options for type 2 diabetes in adolescents and youth (TODAY), 4.5% of obese youth clinically diagnosed with type 2 diabetes (T2D) had genetic variants consistent with maturity onset diabetes of youth (MODY) diagnosis. The course of IS and β-cell function in obese youth with MODY remains unknown.

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Background: Liver function test (LFT) abnormalities, which may reflect underlying pathophysiology, are a well-known feature of Turner syndrome. Less frequently, liver findings may include vascular changes and, rarely, severe liver disease. Although previous studies on children and adolescents suggest a frequency of LFT abnormalities of up to 60%, less is known about the age at onset and natural history.

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Turner syndrome is recognized now as a syndrome familiar not only to pediatricians and pediatric specialists, medical geneticists, adult endocrinologists, and cardiologists, but also increasingly to primary care providers, internal medicine specialists, obstetricians, and reproductive medicine specialists. In addition, the care of women with Turner syndrome may involve social services, and various educational and neuropsychologic therapies. This article focuses on the recognition and management of Turner syndrome from adolescents in transition, through adulthood, and into another transition as older women.

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