Publications by authors named "Yin Chenghong"

Previous studies have reported that pregnant women with non-alcoholic fatty liver disease (NAFLD) face an increased risk of gestational hypertension (GH) and preeclampsia (PE). However, no study has assessed the relationship between the Hepatic Steatosis Index (HSI), a biomarker for NAFLD, in early pregnancy and the subsequent risk of GH and PE. We aimed to investigate the relationship between HSI in early pregnancy and the risks of GH and PE in Chinese women.

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Background: Müllerian duct anomalies (MDAs) are developmental malformations of the female genital tract. Genetic factors linked to MDAs and recent advancements in whole-exome sequencing (WES) have provided innovative perspectives in this field.

Methods: In total, 97 patients with MDAs were recruited.

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The relationship between maternal thyroid-stimulating hormone (TSH), free thyroxine (FT4) and thyroid peroxidase antibody (TPOAb) status and hypertensive disorders of pregnancy (HDP) remains uncertain. This was a prospective cohort study based on the China Birth Cohort Study (CBCS). 36,256 women were included at 6 to 13 gestation from February 2018 to December 2020.

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Background: The relationship between serum ferritin levels and the risk of gestational diabetes mellitus (GDM) remains unclear. This study aimed to investigate the association between serum ferritin levels and the incidence of GDM.

Methods: We conducted a prospective cohort study involving 10,871 pregnant women from the China Birth Cohort Study.

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Background: Evidence on the influence of outdoor artificial light at night (ALAN) on hypothyroidism in pregnant women is scarce. We aimed to investigate the association between outdoor ALAN exposure and hypothyroidism in pregnancy.

Methods: 81,820 pregnant women from the China Birth Cohort Study (CBCS) were analyzed, which recruited from 18 provinces and autonomous regions in China between February 2018 and December 2020.

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Background: The role of inflammation in the development of gestational diabetes mellitus (GDM) has recently become a focus of research. The systemic immune-inflammation index (SII) and systemic inflammation response index (SIRI), novel indices, reflect the body's chronic immune-inflammatory state. This study aimed to investigate the associations between the SII or SIRI and GDM.

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Background: Both assisted reproductive technology and multifetal pregnancy have been reported to be associated with an increased risk of birth defects. However, it is unclear whether multifetal pregnancy is a mediator that increases the risk of birth defects in assisted reproductive technology-conceived pregnancies.

Objective: To investigate the risk of birth defects associated with assisted reproductive technology, and to quantify the mediating effect of multifetal pregnancy between assisted reproductive technology and birth defects.

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Mitophagy serves as a mitochondrial quality control mechanism to maintain the homeostasis of mitochondria and the intracellular environment. Studies have shown that there is a close relationship between mitophagy and apoptosis. Sestrin2 (Sesn2) is a highly conserved class of stress-inducible proteins that play important roles in reducing oxidative stress damage, inflammation, and apoptosis.

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Article Synopsis
  • Acute pancreatitis (AP) can disrupt intestinal microbiota, and angiotensin (Ang)-(1-7) may help protect the intestinal barrier and modify the microbiota.
  • In a study with 31 AP patients and a mouse model, researchers found that Ang-(1-7) administration improved the balance of gut bacteria and reduced pancreatic and intestinal damage.
  • The results suggest that Ang-(1-7) can enhance the abundance of beneficial gut bacteria and restore metabolic functions affected by AP, highlighting its potential as a therapeutic approach.
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The new-generation non-invasive prenatal screening technology (NIPT2.0) is a new method successfully realized in recent years based on high-throughput sequencing to synchronously and accurately detect fetal chromosomal aneuploidies, microdeletion/microduplication syndromes and dominantly inherited monogenic disorders. NIPT2.

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Article Synopsis
  • Müllerian duct anomalies (MDAs) are congenital reproductive tract disorders in females, with recent advancements in whole-exome sequencing (WES) providing new insights into their genetic causes, though many mechanisms remain unclear.
  • In a study involving 97 MDAs patients, researchers identified two novel heterozygous CHD1L variants linked to these anomalies, with variants' pathogenicity confirmed through functional assays and molecular simulations.
  • The study found that the identified variants impaired CHD1L function, affecting protein localization and interactions, leading to a calculated contribution of CHD1L variants to MDAs at 4.12%.
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Background: Compound 861 (Cpd861) is a traditional Chinese herbal compound for the treatment of hepatic fibrosis (HF). In the current investigation, Cpd861 has been demonstrated to have an underlying molecular mechanism and material foundation for the treatment of HF through network pharmacology, Mendelian randomization (MR), and molecular docking.

Methods: Public databases were consulted for Cpd861 constituents and HF targets.

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Background: Remnant cholesterol (RC) reportedly contributes to the development of diabetes mellitus. However, evidence on the relationship between maternal RC and the risk of developing gestational diabetes mellitus (GDM) during pregnancy is limited. This study aimed to assess the relationship between maternal RC and GDM risk during early pregnancy, and explore the potential pathways involved in the relationship between RC levels and GDM risk.

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This study evaluated the association between maternal serum uric acid-to-creatinine ratio (SUA/SCr) in the first trimester and adverse maternal and neonatal outcomes. A prospective birth cohort study was conducted between 2018 and 2021. Logistic regression models and restricted cubic splines were utilized to estimate the associations between the SUA/SCr ratio and feto-maternal pregnancy outcomes.

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This prospective birth cohort study evaluated the association of exposure to PM (diameter ≤2.5 μm), PM (1-2.5 μm), and PM (≤1 μm) with maternal thyroid autoimmunity and function during early pregnancy.

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Article Synopsis
  • Severe acute pancreatitis (SAP) leads to increased macrophage activation and pyroptosis, contributing to immune suppression and lung injury, with cGAS-STING playing a critical role in these processes.* -
  • Experiments using wild type and genetically modified mice, along with in vitro cell tests, demonstrate that disrupting cGAS/STING pathways can reduce inflammasome activation and macrophage death, lessening lung injury related to SAP.* -
  • The study suggests that targeting components of the mtDNA-cGAS-STING pathway could provide therapeutic strategies to mitigate the harmful immune responses associated with SAP-induced lung injury.*
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Article Synopsis
  • The study investigates the link between levothyroxine (LT4) treatment and adverse pregnancy outcomes in pregnant women with elevated TSH levels (2.5-10.0 mIU/L) during the first trimester, focusing on those with varying TPOAb statuses.
  • Using a retrospective cohort analysis of 4,370 pregnant women, the research employed propensity score matching to compare outcomes between those treated with LT4 and those who were not.
  • Findings revealed that LT4 treatment significantly reduced the risk of pregnancy loss but increased the likelihood of small-for-gestational-age infants and preterm birth, particularly among TPOAb-positive women with high-normal TSH levels.
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Mesenchymal stem cell (MSC)-mediated coupling of osteogenesis and angiogenesis is a critical phenomenon in bone formation. Herein, we investigated the role and mechanism of SGMS1 in the osteogenic differentiation of MSCs and, in combination with osteogenesis and angiogenesis, to discover new therapeutic targets for skeletal dysplasia and bone defects. SGMS1 addition accelerated MSC osteogenic differentiation, whereas SGMS1 silencing suppressed this process.

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Background: Premature ovarian insufficiency (POI) is a severe disorder leading to female infertility. Genetic mutations are important factors causing POI. TP63-truncating mutation has been reported to cause POI by increasing germ cell apoptosis, however what factors mediate this apoptosis remains unclear.

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Background: Polycystic ovary syndrome is a metabolic and hormonal disorder that is closely linked to oxidative stress. Within individuals diagnosed with PCOS, changes occur in the ovaries, resulting in an excessive buildup of iron and peroxidation of lipids, both of which may be associated with the occurrence of ferroptosis. Baicalein, a flavonoid found in the roots of Scutellaria baicalensis and widely known as Chinese skullcap, is known for its anti-inflammatory and anti-ferroptotic properties, which protect against various diseases.

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Premature ovarian insufficiency (POI) refers to the decline of ovarian function before the age of 40. POI causes a reduction in or loss of female fertility, accompanied by different degrees of menopausal symptoms, which increases the risk of chronic diseases related to early menopause and seriously affects patients' quality of life and health. It is conservatively estimated that at least one million prepubertal girls and women of reproductive age in China are at risk of iatrogenic POI caused by radiotherapy and chemotherapy every year.

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Background: The heterogeneity of oral glucose tolerance test (OGTT) patterns during pregnancy remains unclear. This study aims to identify latent OGTT patterns in pregnant women and investigate the high-risk population for late-onset gestational diabetes mellitus (GDM).

Methods: This study including 17,723 participants was conducted from 2018 to 2021.

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Background: Subclinical hypothyroidism (SCH) is linked to dyslipidaemia and adverse pregnancy outcomes. However, the impact of dyslipidaemia on the outcome of pregnancy in SCH is unclear.

Methods: We enrolled 36,256 pregnant women and evaluated their pregnancy outcomes.

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Objective: To assess the effectiveness and feasibility of carrier detection for Spinal muscular atrophy (SMA) by using digital PCR assay.

Methods: Peripheral blood samples were collected from 214 pregnant women who were routinely screened for SMA carriers, of which 204 were randomly selected samples and 10 were samples with known copy numbers of SMN1 exons 7 and 8. Samples with known copy numbers of SMN1 exons 7 and 8 were randomly mixed into the experiment to validate the performance of the digital PCR assay.

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