Publications by authors named "Yerong Yu"

The majority of acromegaly and gigantism are caused by growth hormone-secreting pituitary neuroendocrine tumors (PitNETs). Most cases can be cured or controlled by surgery, medical therapy, and/or radiotherapy. However, a few of these tumors are resistant to traditional therapy and always have a poor prognosis.

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  • Cushing's disease leads to higher health risks, and osilodrostat, an oral medication, has shown effectiveness in reducing cortisol levels in patients during two key studies.
  • This analysis included 210 patients, with 27% being of Asian origin; results indicate that both Asian and non-Asian patients showed similar improvements in health measures, although Asian patients required lower doses of osilodrostat.
  • Adverse events (AEs) were common, with Asian patients experiencing more issues related to low cortisol levels and pituitary tumor enlargement compared to their non-Asian counterparts, suggesting greater sensitivity to the treatment in Asian individuals.
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Introduction: Pasireotide, a somatostatin receptor ligand, is approved for treating acromegaly and Cushing's disease (CD). Hyperglycemia during treatment can occur because of the drug's mechanism of action, although treatment discontinuation is rarely required. The prospective, randomized, Phase IV SOM230B2219 (NCT02060383) trial was designed to assess optimal management of pasireotide-associated hyperglycemia.

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  • B01411 is a biosimilar candidate for insulin degludec, aiming to evaluate its pharmacokinetics, pharmacodynamics, and safety compared to the reference product (Tresiba).
  • A phase I study with healthy participants showed bioequivalence between B01411 and insulin degludec, with key metrics falling within the acceptable range for similarity.
  • Both products were found to be well tolerated, with only a minor adverse event reported.
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Background: Giant prolactinoma (> 4 cm in dimension) is a rare disorder. Invasive macroprolactinoma has the potential to cause base of skull erosion and extend into the nasal cavity or even the sphenoid sinus. Nasal bleeding caused by intranasal tumor extension is a rare complication associated with invasive giant prolactinoma.

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Purpose: This study evaluated the effect of body mass index (BMI) on pharmacokinetic (PK) and pharmacodynamic (PD) parameters of insulin degludec in healthy Chinese males, depending on an euglycemic glucose clamp study.

Methods: Sixty-five healthy male subjects were divided into four groups according to quartile of BMI value. Group A: BMI ≤ 20.

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Expression of Concern for 'Novel fatty chain-modified GLP-1R G-protein biased agonist exerts prolonged anti-diabetic effects through targeting receptor binding sites' by Maorong Wang , , 2020, , 8044-8053, https://doi.org/10.1039/C9RA10593J.

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Diet is an important factor that can affect inflammatory processes. Diet-related systemic inflammation is closely linked to periodontitis and tooth loss. However, the role that systemic conditions play in influencing this association remains unclear.

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Background: Adrenal tuberculosis usually presents with bilateral involvement. It has special characteristics in computed tomography (CT) images, such as small size, low attenuation in the center, and peripheral rim enhancement, which differ from those of primary tumors.

Case Summary: A 42-year-old female presented to the hospital with low back pain.

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The therapeutic effect of basal insulin analogs will be sustained at a rather low insulin level. When employing healthy volunteers to assess the pharmacokinetics (PK) and pharmacodynamics (PD) of long-acting insulin preparations by euglycemic clamp techniques, endogenous insulin cannot be ignored and sufficient endogenous insulin inhibition is crucial for the PD and/or PK assessment. This study aimed to explore a way to sufficiently inhibit endogenous insulin secretion.

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  • C-peptide levels must be consistently suppressed during euglycemic clamping to accurately assess insulin pharmacokinetics and pharmacodynamics.
  • This retrospective study involved 33 men who received insulin aspart injections, revealing that insufficient suppression of endogenous insulin can skew results, particularly in glucose infusion rates (GIR) and C-peptide measurements.
  • Two groups were formed based on C-peptide levels post-dosing, demonstrating that improved control of blood glucose is crucial, as unsuppressed endogenous insulin can lead to inaccuracies in evaluating insulin therapy's effects.
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Context: Cushing disease, a chronic hypercortisolism disorder, is associated with considerable morbidity and mortality. Normalizing cortisol production is the primary treatment goal.

Objective: We aimed to evaluate the safety and efficacy of osilodrostat, a potent, orally available 11βhydroxylase inhibitor, compared with placebo in patients with Cushing disease.

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is critical for the development of the pituitary, brain, and face, and mutations may lead to hypopituitarism, intellectual disability, and craniofacial abnormalities. Common mutations are duplications and deletions of the whole or part of , yet only a few cases with point mutations were reported by far. We present a case with growth retardation, small penis, and learning difficulty.

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  • Hyperparathyroidism can lead to hypercalcemia, and spontaneous remission after a hypercalcemic crisis due to parathyroid adenomas is rare.
  • A case study of a 47-year-old male showed that his hypercalcemia resolved on its own after a hypercalcemic crisis, with pathology confirming intracystic hemorrhage in his adenomas.
  • The study emphasizes evaluating clinical symptoms and parathyroid function changes to determine the best surgical timing in similar cases.
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Purpose: Poor sleep accompanied by elevated TSH (thyroid stimulating hormone) levels is not uncommon since TSH secretion is controlled by the circadian rhythm. However, the relationship between poor sleep and TSH elevation is unclear; hence, we aimed to elucidate this relationship by conducting a cross-sectional and longitudinal study.

Methods: Participants with isolated elevated (N = 168) and normal (N = 119) TSH concentrations were recruited, and the Pittsburgh Sleep Quality Index (PSQI) was used to assess the sleep status.

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Insulin glargine (IGlar) and LY2963016 (LY IGlar) are long-acting insulin analogs with identical primary amino acid sequences. We conducted a randomized, open-label, 2-treatment, 2-period, crossover study in healthy Chinese subjects to evaluate the relative bioavailability of LY IGlar to IGlar and pharmacokinetic (PK) and pharmacodynamic (PD) characteristics of LY IGlar. Subjects (n = 58) were randomized to receive single subcutaneous doses (0.

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Purpose: Pasireotide is an effective treatment for acromegaly and Cushing's disease, although treatment-emergent hyperglycemia can occur. The objective of this study was to assess incretin-based therapy versus insulin for managing pasireotide-associated hyperglycemia uncontrolled by metformin/other permitted oral antidiabetic drugs.

Methods: Multicenter, randomized, open-label, Phase IV study comprising a core phase (≤ 16-week pre-randomization period followed by 16-week randomized treatment period) and optional extension (ClinicalTrials.

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  • The study compared the pharmacokinetics (PK) and pharmacodynamics (PD) of two rapid-acting insulin products: a new biosimilar (RD10046) and NovoRapid, aimed at controlling post-meal blood glucose levels.
  • Participants were healthy Chinese males who received both insulin products in a crossover trial, completing all treatment periods without any adverse events like hypoglycemia or allergic reactions.
  • Results showed that PK and PD measures were similar for both products, indicating that RD10046 is bioequivalent to NovoRapid, as the 90% confidence intervals met the acceptance criteria.
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Background: Hypercalcemia associated with acromegaly is mostly parathyroid hormone (PTH)-dependent, being caused by parathyroid hyperplasia or adenoma, which are common in individuals with multiple endocrine adenomatosis-1 (MEN-1). The rare occurrence of non-PTH-dependent hypercalcemia associated with acromegaly is attributable to complex factors involving increased intestinal calcium absorption, enhanced bone calcium release, and reduced urinary calcium elimination. Although patients with acromegaly often have mild hyperphosphatemia and hypercalciuria, clinically significant hypercalcemia is extremely rare.

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  • Bilateral inferior petrosal sinus sampling (BIPSS) is the standard invasive method for diagnosing ACTH-dependent Cushing's syndrome (CS), but it's not always easy to access.
  • A study evaluated the effectiveness of two non-invasive tests—24-hour urinary free cortisol (UFC) levels after a high-dose dexamethasone suppression test and plasma ACTH/cortisol levels after a desmopressin stimulation test—in distinguishing between Cushing's disease (CD) and ectopic ACTH-dependent CS.
  • The combination of these two tests showed high sensitivity (95.5%) and positive predictive value (98.4%) for diagnosing CD, suggesting they could reduce the need for the more invasive BIPSS procedure.
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Purpose: The present study compared the interindividual variability in the pharmacodynamic (PD) and pharmacokinetic (PK) properties of a short-acting recombinant human insulin to those of insulin aspart through manual euglycemic glucose clamp tests.

Methods: Sixty healthy Chinese male volunteers were randomly assigned to receive human insulin or insulin aspart, administered via SC injection (0.2 U/kg).

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Objective: To investigate the diagnostic value of different captopril challenge test (CCT) diagnostic criteria for diagnosing primary aldosteronism (PA).

Methods: We collected the clinical data of 184 patients with hypertension retrospectively in West China Hospital of Sichuan University. Receiver operating characteristic (ROC) curves were used to analyze the post-CCT efficacy of aldosterone renin activity ratio (ARR), plasma aldosterone concentration (PAC), plasma renin activity (PRA) and PAC suppression rate for PA diagnosis.

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