Publications by authors named "Curry C"

Background: Associations between early-life menstrual cycle characteristics (MCC) and gestational diabetes (GDM) remain unclear.

Objectives: To evaluate associations between early-life MCCs and GDM in first pregnancy, across pregnancies and its recurrence.

Methods: This analysis included participants from a US-based digital cohort enrolled between 11/2019 and 9/2023 who provided consent, completed relevant surveys, were without diabetes and aged ≥18 at first pregnancy (n = 30,473).

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Background: The objective of this study was to compare the accuracy of available tests for pyuria, including newer automated tests, and to examine the implications of requiring them for the diagnosis of urinary tract infections (UTIs).

Methods: We included children between 1 and 36 months of age undergoing bladder catheterization for suspected UTIs who presented to 1 of 3 pediatric centers. Using a positive urine culture result as the reference standard, we compared the sensitivity of 5 modalities for assessing pyuria at the cutoffs most often used clinically for detecting children with a positive culture result: leukocyte esterase on a dipstick, white blood cell (WBC) count on manual microscopy with and without using a hemocytometer, automated WBC enumeration using flow cytometry, and automated WBC enumeration using digital imaging with particle recognition.

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Background: Research in recent years has increasingly highlighted the relationship between exposure to potentially morally injurious events (PMIEs) and poor mental health outcomes. Human trafficking survivors often report exposure to many traumatic and PMIEs and given the complexities of trafficking exploitation, survivors may be especially vulnerable to moral injury. Despite this, no research has investigated experiences of PMIEs and moral injury in human trafficking survivors.

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Jansen-de Vries syndrome (JdVS) is an autosomal dominant neurodevelopmental disorder with intellectual disability and gastrointestinal (GI) abnormalities, including recurrent vomiting. This study aimed to understand the frequency and severity of GI symptoms in JdVS patients and to investigate the potential association with cyclic vomiting syndrome (CVS), which has not been previously reported. An international online survey assessed the prevalence and features of CVS and GI disorders in JdVS patients using Rome IV Criteria.

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Human neural organoid models have become an important tool for studying neurobiology. However, improving the representativeness of neural cell populations in such organoids remains a major effort. In this work, we compared Matrigel, a commercially available matrix, to a neural cadherin (N-cadherin) peptide-functionalized gelatin methacryloyl hydrogel (termed GelMA-Cad) for culturing cortical neural organoids.

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  • A study evaluated the prevalence of androgen excess (AE) symptoms in 24,435 participants from a U.S. digital cohort, focusing on signs like hirsutism, chin hair, hair loss, and acne from November 2019 to December 2022.
  • Results revealed that possible hirsutism was at 6.9%, chin hair at 12.6%, hair loss at 1.7%, and moderate to severe acne at 31.8%, with variations noted across different age groups and demographics.
  • The findings suggest that AE symptoms differ by age, ethnicity, and body mass index, indicating the need for more inclusive health evaluations in diverse populations.
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Background: While it is known that vital signs and behaviors change during pregnancy, there is limited data on timing and scale of changes for sensor-derived health metrics across pregnancy and postpartum. Wearable technology provides an opportunity to understand physiologic and behavioral changes across pregnancy with greater detail, more frequent measurements, and improved accuracy. The aim of this study is to describe changes in physiologic and behavioral sensor-based health metrics during pregnancy and postpartum in the Apple Women's Health Study (AWHS) and their relationship to demographic factors.

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High-intensity, short-pulse lasers are crucial for generating energetic electrons that produce high-energy-density (HED) states in matter, offering potential applications in igniting dense fusion fuels for fast ignition laser fusion. High-density targets heated by these electrons exhibit spatially non-uniform and highly transient conditions, which have been challenging to characterize due to limitations in diagnostics that provide simultaneous high spatial and temporal resolution. Here, we employ an X-ray Free Electron Laser (XFEL) to achieve spatiotemporally resolved measurements at sub-micron and femtosecond scales on a solid-density copper foil heated by laser-driven fast electrons.

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  • Researchers identified bi-allelic disruptive variants as the cause of autosomal recessive intellectual developmental disorder type 65, while dominant variants are harder to link to specific traits due to their presence in unaffected individuals.
  • The study involved a retrospective analysis of 21 individuals with likely pathogenic variants, focusing on clinical information and molecular data from their families.
  • Key findings revealed that those with dominant disruptive variants exhibited more developmental and behavioral problems, while individuals with dominant missense variants had a higher occurrence of renal and skin anomalies, enhancing the understanding of the related neurodevelopmental disorder.
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Objectives: To determine the frequency of early meropenem concentration target attainment (TA) in critically ill children with severe sepsis; to explore clinical, therapeutic, and pharmacokinetic factors associated with TA; and to assess how fluid resuscitation and volume status relate to early TA.

Design: Retrospective analysis of prospective observational cohort study.

Setting: PICU in a single academic quaternary care children's hospital.

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Purpose: Rural adolescent pregnancy is a serious public health issue, largely due to low contraceptive use. Existing data focuses on urban populations. Using a positive youth development framework, we examine associations between modifiable protective factors and birth control use in a rural population.

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Background: Medical mistrust (MM) is seen as a barrier to assessing healthcare needs and addressing health disparities; however, limited literature has focused on assessing MM for vulnerable populations, especially racial/ethnic minority and sexual/gender minority youth and young adults (YYA).

Methods: Between February 2021 and March 2022, we conducted the Youth and Young Adults COVID-19 Study, a prospective cohort of minoritized YYA aged 14 to 24 years (n = 1027), within the United States and its territories. Participants were recruited through a combination of paid social media ads, outreach with organizations serving marginalized youth, and an existing registry, targeting racial and ethnic minority and LGBTQ + youth for a study on COVID-19 health behaviors.

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Background: Meropenem, a β-lactam antibiotic commonly prescribed for severe infections, poses dosing challenges in critically ill patients due to highly variable pharmacokinetics.

Objectives: We sought to develop a population pharmacokinetic model of meropenem for critically ill paediatric and young adult patients.

Patients And Methods: Paediatric intensive care unit patients receiving meropenem 20-40 mg/kg every 8 h as a 30 min infusion were prospectively followed for clinical data collection and scavenged opportunistic plasma sampling.

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  • This text indicates a correction to a previously published article.
  • The specific article is identified by its DOI: 10.1016/j.isci.2024.109122.
  • The correction ensures that the information or data presented in the article is accurate and up to date.
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  • Biallelic variants in the ZBTB11 gene are linked to a rare intellectual developmental disorder known as MRT69, which shows a variety of clinical symptoms.
  • The study focused on analyzing clinical and genetic traits of 29 individuals (ages 2-50) with these variants, finding diverse neurodevelopmental issues and complex movement disorders among the patients.
  • Results revealed that many patients had abnormal movements (like ataxia and dystonia) and cataracts, with one patient showing improvement from deep brain stimulation, contributing 13 new genetic variants to the understanding of ZBTB11-related disorders.
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  • Early menarche is linked to negative health outcomes, and trends in the US show it's happening earlier, but more research is needed on how factors like socioeconomic status and BMI impact this.
  • The study aims to analyze trends in age at menarche and how long it takes to achieve regular menstrual cycles while considering early-life BMI's role as a mediator.
  • Data from 71,341 female participants reveal that the average age of menarche decreased over the decades, with a notable increase in cases of early and very early menarche.
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Carpenter syndrome (CRPTS) is a rare autosomal recessive condition caused by biallelic variants in genes that encode negative regulators of hedgehog signalling (RAB23 [CRPT1] or, more rarely, MEGF8 [CRPT2]), and is characterised by craniosynostosis, polysyndactyly, and other congenital abnormalities. We describe a further six families comprising eight individuals with MEGF8-associated CRPT2, increasing the total number of reported cases to fifteen, and refine the phenotype of CRPT2 compared to CRPT1. The core features of craniosynostosis, polysyndactyly and (in males) cryptorchidism are almost universal in both CRPT1 and CRPT2.

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  • Polycystic ovary syndrome (PCOS) is a common condition that causes irregular menstrual cycles and is linked to cardiovascular and metabolic issues, but more research is needed on its specific relationships and interventions.
  • The study aimed to analyze how PCOS, time to menstrual regularity from menarche, and irregular cycles impact the occurrence of various cardiometabolic conditions in participants using the Apple Research app.
  • The research involved a large group of US-based individuals, finding that 12.3% had PCOS, with a focus on various cardiovascular and metabolic health outcomes, while also considering how lifestyle factors may influence these associations.
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PARP2 is a DNA-dependent ADP-ribosyl transferase (ARTs) enzyme with Poly(ADP-ribosyl)ation activity that is triggered by DNA breaks. It plays a role in the Base Excision Repair pathway, where it has overlapping functions with PARP1. However, additional roles for PARP2 have emerged in the response of cells to replication stress.

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  • - The text discusses two difficult cases of pediatric/adolescent aggressive mature B-cell non-Hodgkin lymphoma (B-NHL), specifically within Burkitt and diffuse large B-cell lymphoma categories.
  • - Both cases showed unique lymphoma cell characteristics and genetic abnormalities, including complex karyotypes and mutations identified through advanced sequencing methods.
  • - The authors concluded that these cases could be classified as "DLBCL-NOS with rearrangement" and highlighted the diagnostic and treatment challenges faced, especially for adolescents and young adults.
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  • Aging leads to a dominance of specific variants of hematopoietic stem cells (HSCs) in blood cell production, which may negatively impact health due to their differentiated progeny.* -
  • Somatic mutations in the DNMT3A gene are linked to this clonal dominance, and interactions with high-fat diets (HFD) were studied in mice to understand their combined effects.* -
  • The research found that reduced DNMT3A in the context of HFD promotes weight gain and inflammation by triggering pro-inflammatory pathways and abnormal DNA methylation during the differentiation of myeloid cells.*
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Introduction: For adult trauma patients, the likelihood of receiving treatment at a hospital properly equipped for trauma care can vary by race and sex. This study examines whether a pediatric patient's race/ethnicity and sex are associated with treatment at a high acuity trauma hospital (HATH).

Materials And Methods: Using the 2017 National Inpatient Sample, we identified pediatric trauma patients ( ≤16 y) using International Classification of Diseases-10 codes.

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Objective: To automate the generation of three validated nephrometry scoring systems on preoperative computerised tomography (CT) scans by developing artificial intelligence (AI)-based image processing methods. Subsequently, we aimed to evaluate the ability of these scores to predict meaningful pathological and perioperative outcomes.

Patients And Methods: A total of 300 patients with preoperative CT with early arterial contrast phase were identified from a cohort of 544 consecutive patients undergoing surgical extirpation for suspected renal cancer.

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Objectives: Music is helpful to young people in healthcare contexts, but less is known about the acceptability of music-based interventions for youth living at home with chronic pain who may be struggling to attend school and participate in social activities. The Songs of Love (SOL) foundation is a national nonprofit organization that creates free, personalized, original songs for youth facing health challenges. The aims of this study were (1) to assess acceptability of SOL from the perspective of youth with chronic pain receiving a song and singer-songwriters who created the songs, and (2) to explore the role of music more generally in the lives of young people living with pain.

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  • - Over the past 50-60 years, genetics and dysmorphology have become essential in medicine, helping diagnose rare diseases and informing various medical specialties.
  • - Both fields heavily depend on molecular geneticists for identifying genes linked to disorders, showcasing their interconnectedness in patient care.
  • - The memoirs collected highlight the personal journeys of professionals in these specialties, emphasizing their adaptability and the chance experiences that led them to enjoy a career in genetics and dysmorphology.
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