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CompletedNCT05035966Updated Sep 9, 2021

Association of β-amyloid 40 and 42 With Prediabetes

An observational study in PreDiabetes, sponsored by Liegang Liu. Completed. Open to participants aged 30 Years to 80 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2021-09-09.

Sponsored by Liegang Liu · Observational

Study type
Observational
Model
Case-control
Time perspective
Retrospective
Enrollment
1,442
Ages
30 Years to 80 Years
Sex
All
01

Study summary

Background: Previous epidemiological and animal studies have suggested a strong relationship between prediabetes and Alzheimer's disease. Recently, we demonstrated that plasma β-amyloid (Aβ), a potential biomarker for Alzheimer's disease, was elevated in individuals with type 2 diabetes. However, few studies have investigated the associations of plasma Aβ40 and Aβ42 concentrations with prediabetes.

Objective: we aimed to investigate the associations of plasma Aβ40 and Aβ42 concentrations with risk of prediabetes in two independent studies.

Design: We performed a case-control study and a nested case-control study within a prospective cohort study. In the case-control study, we included 571 newly diagnosed individuals with prediabetes and 571 control participants. Prediabetes individuals were consecutively recruited from subjects who attended the outpatient clinics of Department of Endocrinology at Tongji Medical College Hospital from 2012 to 2015. Concomitantly, we recruited healthy controls from a general population undergoing a routine health checkup in the same hospital. One healthy control was selected at random for each prediabetes individuals according to age (±3 years) and sex. The inclusion criteria of participants were as follows: age ≥30 and ≤80 years, BMI \<40 kg/m2, no history of prediabetes and diabetes mellitus, no history of receiving pharmacological treatment for hyperlipidemia, nor any clinically systemic disease, any acute illness, and chronic inflammatory or any infective disease. An independent nested case-control study was conducted within an ongoing cohort study, namely the Tongji-Ezhou cohort. Briefly, 5533 participants, including 3101 retired employees and 2432 working employees, were enrolled from Echeng Stell and received healthcare for a baseline investigation between 2013 and 2015. The first follow-up for all participants was finished by mid-2020. Considering the low incidence of prediabetes among young working employees, we performed the nested case-control study among retired employees. During the follow-up, 119 new-onset prediabetes cases were diagnosed within the retired employees according to fasting plasma glucose. We randomly selected the control participants who matched 2:1 to the cases by age (±3 years) and sex from the retired employees with normal fasting plasma glucose. The inclusion criteria were the same as the case-control study; 2 new-onset prediabetes cases aged >80 years were excluded. Additionally, 17 cases without enough plasma were excluded. Finally, 100 individuals with new-onset prediabetes and 200 well-matched control participants were included for the analysis of the nested case-control study. These two studies were approved by the Ethics and Human Subject Committee of Tongji Medical College. All enrolled participants in the two studies were of Chinese Han ethnicity and provided informed written consent. Plasma Aβ40 and Aβ42 concentrations were simultaneously measured by validated assay platforms from Meso Scale Discovery (MSD; Rockville, MD, USA).

02

Conditions studied

  • PreDiabetes

Keywords

  • β-amyloid 40
  • β-amyloid 42
  • prediabetes
03

In context

Prediabetic State

999 studies on the registry are indexed under Prediabetic State; 238 are open to participants now.

This study's enrollment of 1,442 is above the median of 216 across 128 observational studies indexed under Prediabetic State.

Browse Prediabetic State studies →

Lead sponsor

Liegang Liu is the lead sponsor of 5 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
30 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

All the participants enrolled were of Chinese Han ethnicity. They gave informed written consent to the study and did not take any medication known to affect glucose tolerance or insulin secretion before participation.

Inclusion criteria

  • Age ≥30 and ≤80 years, BMI \<40 kg/m2, screened for prediabetes or diabetes, and with enough plasma collected for β-amyloid 40 and 42 detection.

Exclusion criteria

Exclusion Criteria:

  • History of diabetes mellitus and prediabetes, pharmacological treatment for hyperlipidaemia, any clinically systemic disease, any acute illness, chronic inflammatory disease or any infective disease.
05

Study design

Observational model
Case-control
Time perspective
Retrospective
Enrollment
1,442 participants (actual)
Patient registry
No

Groups and cohorts

  • Prediabetes

    In the case-control study, prediabetes was diagnosed according to the diagnostic criteria recommended by the WHO in 1999. Prediabetes was defined as impaired fasting glucose (FPG ≥6.1 mmol/L and \<7.0 mmol/L, and 2-h post-glucose load \<7.8 mmol/L) and/or impaired glucose tolerance (FPG \<6.1 mmol/L, and 2-h post-glucose load ≥7.8 mmol/L and \<11.1 mmol/L). In the nested case-control study, new-onset prediabetes was defined as FPG ≥6.1 mmol/L and \<7.0 mmol/L.

    Other: Plasma β-amyloid 40 and 42 concentration

  • Healthy control

    In the case-control study, healthy control was defined as FPG \<6.1 mmol/L and 2-h post-glucose load \<7.8 mmol/L. In the nested case-control study, healthy control was defined as FPG \<6.1 mmol/L.

    Other: Plasma β-amyloid 40 and 42 concentration

Interventions

  • OtherPlasma β-amyloid 40 and 42 concentration

    Plasma β-amyloid 40 and 42 concentrations were simultaneously measured by validated assay platforms from Meso Scale Discovery (MSD; Rockville, MD, USA).

06

What researchers measure

Primary outcomes

  1. Prediabetes

    In the case-control study, prediabetes was diagnosed in accordance with the diagnostic criteria recommended by WHO in 1999; in the nested case-control study, new-onset prediabetes was confirmed as FPG ≥7.0 mmol/l.

    Time frame: Newly diagnosed prediabetes in the case-control study was diagnosed between 2012 and 2015; new-onset prediabetes in the nested case-control study was identified between 2013 and 2020.

07

Study locations

No study locations are listed for this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 9, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05035966
Lead sponsor
Liegang Liu
Responsible party
Liegang Liu (Professor, Huazhong University of Science and Technology) — Sponsor-investigator
First posted
Sep 5, 2021
Start date
Jan 1, 2012
Primary completion
Dec 31, 2015
Completion
Jun 30, 2020
Last update
Sep 9, 2021

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2021. You cannot join it, but the record below documents what was studied.

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