このページは自動翻訳されたものであり、翻訳の正確性は保証されていません。を参照してください。 英語版 ソーステキスト用。

Application of FreeStyle Libre 2 for Evaluating Glycemic Variability Characteristics in Patients With Extreme Glucose Metabolism Phenotypes

2026年5月31日 更新者:Ren qian、Peking University People's Hospital
This cross-sectional study aims to further subdivide diabetes mellitus into more homogeneous subgroups by focusing on extreme glucose metabolism phenotypes, including monogenic diabetes with β cell dysfunction, hyperinsulinemia caused by excessive β cell secretion, and postprandial hypoglycemia phenotypes. By utilizing continuous glucose monitoring (CGM) technology and the FreeStyle Libre 2 glucose monitoring device, this study will evaluate glycemic variability patterns in patients with extreme glucose metabolism phenotypes and perform comparative analyses using existing CGM data from healthy populations and patients with type 2 diabetes in our center's database. The study aims to address current gaps in understanding glycemic variability characteristics under extreme β cell functional states, provide novel dynamic monitoring evidence to support early identification, precise classification, and personalized management of these special metabolic states, and simultaneously screen for biomarkers to enable more accurate disease identification, thereby offering potential avenues for improving personalized treatment of diabetes mellitus.

調査の概要

状態

まだ募集していません

詳細な説明

Diabetes mellitus is one of the leading causes of death and disability worldwide, affecting individuals regardless of race, sex, or age. Over the past decade, the prevalence of diabetes mellitus in China has increased markedly. Statistics indicate that there were 140.9 million adults with diabetes mellitus in China in 2021, and this number is projected to rise to 174.4 million by 2045.

Monogenic diabetes refers to diabetes mellitus caused by mutations in a single gene and accounts for approximately 1%-5% of all diabetes mellitus cases. Monogenic diabetes results from a single pathogenic defect in one of more than 40 genes. Since the type 2 diabetes-like presentation in young individuals was termed maturity-onset diabetes of the young (MODY) by Fajans and characterized by an autosomal dominant inheritance pattern, understanding of the phenotypic and genetic heterogeneity of monogenic diabetes has continued to expand. The main categories of monogenic diabetes include MODY, neonatal diabetes mellitus (NDM), and syndromic diabetes. In monogenic diabetes, high-penetrance variants predominantly cause severe impairment of β cell development and insulin secretion, leading to diabetes mellitus independent of other risk factors. In recent years, substantial progress has been made in elucidating the genetic defects underlying monogenic diabetes, improving diagnostic accuracy for rare subtypes, deepening understanding of patients' clinical courses, and contributing to the identification of optimal treatment strategies through precision medicine approaches. However, many aspects of this disease remain insufficiently characterized, including characteristic glycemic profiles and objective, quantifiable indicators applicable to clinical differential diagnosis. Therefore, further research is urgently needed.

Type 2 diabetes mellitus (T2DM) is a multifactorial disease resulting from the combined effects of genetic and environmental factors and accounts for approximately 96% of diabetes mellitus cases worldwide. The pathophysiology of T2DM is characterized by insulin resistance, pancreatic β cell dysfunction, and chronic inflammation. Hyperinsulinemia and insulin resistance may occur several years before the clinical onset of T2DM. Previous studies have demonstrated that more than 75% of individuals in the United States exhibit increased insulin secretion during oral glucose tolerance testing (OGTT) despite normal glucose clearance. This finding suggests that in a substantial proportion of the population, hyperinsulinemia may represent the earliest warning signal of metabolic disease risk, even in the presence of normal glucose tolerance. Targeted lifestyle interventions aimed at hyperinsulinemia, such as increased resistance training, nutritional strategies, and improved sleep, have been shown to produce immediate and sustained improvements in insulin resistance. However, within this gray zone spanning the progression from normal glucose tolerance to overt diabetes mellitus, characteristic glycemic profiles have not yet been clearly defined. Therefore, exploring glycemic variability characteristics is essential for elucidating the onset and progression of insulin resistance and type 2 diabetes mellitus, as well as for enabling early intervention.

The oral glucose tolerance test (OGTT), as the most widely used diagnostic gold standard for assessing glycemic characteristics, employs a standardized 75 g glucose load to evaluate early-phase and second-phase β cell secretory capacity following glucose stimulation. As an artificially constructed experimental simulation, OGTT does not reflect daily physiological conditions and can capture only short-term, single-day glycemic variability, thus failing to represent true blood glucose trajectories. Continuous glucose monitoring (CGM) can dynamically and continuously reflect interstitial fluid glucose levels in real time, providing critical information on the amplitude, frequency, and patterns of glycemic variability that cannot be obtained through traditional point blood glucose testing. CGM has become animportant tool for refined diabetes mellitus management. This technology provides technical support for delineating characteristic glycemic variability patterns under different insulin secretion states.

Accordingly, this study will use CGM to objectively and quantitatively compare glycemic variability parameters and patterns among four groups: patients with β cell dysfunction monogenic diabetes versus patients with type 2 diabetes mellitus, and patients with hyperinsulinemia versus healthy controls. This approach will reveal the effects of extreme β cell function on diurnal glycemic variability patterns and characterize distinctive dynamic glycemic profiles. In addition, this study will screen for biomarkers to facilitate early identification, diagnosis, and treatment of this specific type of diabetes mellitus, while simultaneously deepening understanding of glycemic characteristics in the early stages of insulin resistance and providing a theoretical basis for subsequent precise prevention and intervention.

Primary study objective: To evaluate glycemic variability patterns in patients with extreme glucose metabolism phenotypes, including β-MND, hyperinsulinemia, and postprandial hypoglycemia phenotypes.

Secondary study objective:

  1. To assess differences in blood glucose profiles between individuals with extreme glucose metabolism phenotypes and healthy populations, as well as patients with type 2 diabetes mellitus (T2DM), particularly among comparable T2DM subgroups.
  2. To screen for biomarkers that enable more accurate identification of this disease.

研究の種類

観察的

入学 (推定)

120

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

はい

サンプリング方法

非確率サンプル

調査対象母集団

this study will use CGM to objectively and quantitatively compare glycemic variability parameters and patterns among four groups: patients with β cell dysfunction monogenic diabetes versus patients with type 2 diabetes mellitus, and patients with hyperinsulinemia versus healthy controls. This approach will reveal the effects of extreme β cell function on diurnal glycemic variability patterns and characterize distinctive dynamic glycemic profiles.

60 patients with β cell dysfunction monogenic diabetes and 60 patients with hyperinsulinemia and normal glucose tolerance who meet the inclusion criteria outlined will be recruited from the endocrinology outpatient clinic of our hospital.

Groups A1 and A2, as well as Groups B1 and B2, will be matched at a 1:1 ratio by age, sex, and BMI. In addition, Groups A1 and A2 will be matched at a 1:1 ratio by HbA1c.

説明

  1. Inclusion Criteria:

    1. Group A1:

      • Age ≥ 18 years;
      • Patients with β cell dysfunction monogenic diabetes confirmed by DNA sequencing or other diagnostic testing.
    2. Group A2:

      • Age ≥ 18 years;
      • Patients with confirmed type 2 diabetes mellitus;
      • Derived from this center's existing continuous glucose monitoring (CGM) database.
    3. Group B1:

      • Age ≥ 18 years;
      • Normal fasting plasma glucose (≥ 3.6 and < 6.1 mmol/L) and normal 2-hour plasma glucose during OGTT (≥ 3 and < 7.8 mmol/L);
      • Fasting insulin ≥ 25 µU/mL and/or 2-hour insulin during OGTT greater than 10 times the fasting insulin level.
    4. Group B2:

      • Age ≥ 18 years;
      • Normal glucose tolerance meeting the 2024 ADA criteria: fasting plasma glucose < 5.6 mmol/L, 2-hour plasma glucose during OGTT < 7.8 mmol/L;
      • According to laboratory reference standards, fasting insulin ≥ 2.6 and < 25 µU/mL, and 2-hour insulin during OGTT 5-10 times the fasting insulin level.
      • Derived from this center's existing continuous glucose monitoring (CGM) database.
  2. Exclusion Criteria:

    1. Neonates younger than 4 months of age (congenital diabetes);
    2. Pregnancy;
    3. Patients with positive pancreatic autoantibody test results;
    4. Patients with severe cardiovascular or cerebrovascular diseases, hepatic disease, or renal disease;
    5. Patients who have participated in other clinical trials.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

コホートと介入

グループ/コホート
Group A : diabetes mellitus group
Group A1 (patients with β cell dysfunction monogenic diabetes): 60 cases; Group A2 (patients with type 2 diabetes mellitus): 60 cases
Group B : normal glucose tolerance group
Group B1 (normal glucose tolerance with fasting / postprandial hyperinsulinemia): 60 cases; Group B2 (normal glucose tolerance with normal insulin levels): 60 cases

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
mean blood glucose in mmol/L
時間枠:The study is a cross-sectional study, patients wil wear a CGM for 14 days after enrollment, and will not wear it afterwards.
glycemic variability data
The study is a cross-sectional study, patients wil wear a CGM for 14 days after enrollment, and will not wear it afterwards.
glucose management indicator (GMI) in %
時間枠:The study is a cross-sectional study, patients wil wear a CGM for 14 days after enrollment, and will not wear it afterwards.
glycemic variability data
The study is a cross-sectional study, patients wil wear a CGM for 14 days after enrollment, and will not wear it afterwards.
highest glucose values in mmol/L
時間枠:The study is a cross-sectional study, patients wil wear a CGM for 14 days after enrollment, and will not wear it afterwards.
glycemic variability data
The study is a cross-sectional study, patients wil wear a CGM for 14 days after enrollment, and will not wear it afterwards.
lowest glucose values in mmol/L
時間枠:The study is a cross-sectional study, patients wil wear a CGM for 14 days after enrollment, and will not wear it afterwards.
glycemic variability data
The study is a cross-sectional study, patients wil wear a CGM for 14 days after enrollment, and will not wear it afterwards.
coefficient of variation (CV)
時間枠:The study is a cross-sectional study, patients wil wear a CGM for 14 days after enrollment, and will not wear it afterwards.
glycemic variability data
The study is a cross-sectional study, patients wil wear a CGM for 14 days after enrollment, and will not wear it afterwards.
mean amplitude of glycemic excursions (MAGE) in mmol/L
時間枠:The study is a cross-sectional study, patients wil wear a CGM for 14 days after enrollment, and will not wear it afterwards.
glycemic variability data
The study is a cross-sectional study, patients wil wear a CGM for 14 days after enrollment, and will not wear it afterwards.
standard deviation of blood glucose (SDBG) in mmol/L
時間枠:The study is a cross-sectional study, patients wil wear a CGM for 14 days after enrollment, and will not wear it afterwards.
glycemic variability data
The study is a cross-sectional study, patients wil wear a CGM for 14 days after enrollment, and will not wear it afterwards.
mean of daily differences (MODD) in mmol/L
時間枠:The study is a cross-sectional study, patients wil wear a CGM for 14 days after enrollment, and will not wear it afterwards.
glycemic variability data
The study is a cross-sectional study, patients wil wear a CGM for 14 days after enrollment, and will not wear it afterwards.
average daily risk range (ADRR)
時間枠:The study is a cross-sectional study, patients wil wear a CGM for 14 days after enrollment, and will not wear it afterwards.
glycemic variability data
The study is a cross-sectional study, patients wil wear a CGM for 14 days after enrollment, and will not wear it afterwards.
largest amplitude of glycemic excursions (LAGE) in mmol/L
時間枠:The study is a cross-sectional study, patients wil wear a CGM for 14 days after enrollment, and will not wear it afterwards.
glycemic variability data
The study is a cross-sectional study, patients wil wear a CGM for 14 days after enrollment, and will not wear it afterwards.
high blood glucose index (HBGI)
時間枠:The study is a cross-sectional study, patients wil wear a CGM for 14 days after enrollment, and will not wear it afterwards.
glycemic variability data
The study is a cross-sectional study, patients wil wear a CGM for 14 days after enrollment, and will not wear it afterwards.
low blood glucose index (LBGI)
時間枠:The study is a cross-sectional study, patients wil wear a CGM for 14 days after enrollment, and will not wear it afterwards.
glycemic variability data
The study is a cross-sectional study, patients wil wear a CGM for 14 days after enrollment, and will not wear it afterwards.
time in range (TIR) in %
時間枠:The study is a cross-sectional study, patients wil wear a CGM for 14 days after enrollment, and will not wear it afterwards.
glycemic variability data
The study is a cross-sectional study, patients wil wear a CGM for 14 days after enrollment, and will not wear it afterwards.
time above range (TAR) in %
時間枠:The study is a cross-sectional study, patients wil wear a CGM for 14 days after enrollment, and will not wear it afterwards.
glycemic variability data
The study is a cross-sectional study, patients wil wear a CGM for 14 days after enrollment, and will not wear it afterwards.
time below range (TBR) in %
時間枠:The study is a cross-sectional study, patients wil wear a CGM for 14 days after enrollment, and will not wear it afterwards.
glycemic variability data
The study is a cross-sectional study, patients wil wear a CGM for 14 days after enrollment, and will not wear it afterwards.

二次結果の測定

結果測定
メジャーの説明
時間枠
weight in kilograms
時間枠:The study is a cross-sectional study, and the above indicators were measured only once at the initial enrollment.
weight and height will be combined to report BMI in kg/m^2
The study is a cross-sectional study, and the above indicators were measured only once at the initial enrollment.
height in meters
時間枠:The study is a cross-sectional study, and the above indicators were measured only once at the initial enrollment.
weight and height will be combined to report BMI in kg/m^2
The study is a cross-sectional study, and the above indicators were measured only once at the initial enrollment.

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年5月25日

一次修了 (推定)

2026年12月25日

研究の完了 (推定)

2027年1月9日

試験登録日

最初に提出

2026年4月14日

QC基準を満たした最初の提出物

2026年4月26日

最初の投稿 (実際)

2026年5月4日

学習記録の更新

投稿された最後の更新 (実際)

2026年6月2日

QC基準を満たした最後の更新が送信されました

2026年5月31日

最終確認日

2026年5月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • 2026PHB206-001

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

購読する