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Association Between TMAO and Diabetes

Зөвхөн бүртгэлтэй хэрэглэгчид л нийтлэл орчуулах боломжтой
Нэвтрэх / Бүртгүүлэх
Холбоосыг санах ойд хадгалдаг
СтатусДууссан
Ивээн тэтгэгчид
Liegang Liu

Түлхүүр үгс

Хураангуй

Background: The association of trimethylamine-N-oxide (TMAO), a microbiota dependent metabolite from dietary choline and carnitine, with type 2 diabetes was inconsistent.
Objective: The investigators planned to investigate the association between plasma TMAO and newly diagnosed type 2 diabetes as well as whether the association could be modified by the TMAO-generating enzyme flavin monooxygenase 3 (FMO3) polymorphisms.
Design: This is an age- and sex-matched case-control study of 2694 participants: 1346 newly diagnosed cases of type 2 diabetes and 1348 controls. The patients of newly diagnosed type 2 diabetes were consecutively recruited from those attending for the first time the outpatient clinics of Department of Endocrinology, Tongji Medical College Hospital, Wuhan, China, from 2012 January to December 2014. Concomitantly, the investigators recruited healthy individuals who were frequency-matched by age (±5 years) and sex to patients from an unselected population undergoing a routine health check-up in the same hospital. The inclusion criteria for controls and newly diagnosed type 2 diabetes were: age ≥ 30 years, body mass index (BMI) < 40 kg/m2, no history of a diagnosis of diabetes and no history of receiving pharmacological treatment for hyperlipidaemia or hypertension. Patients with clinically significant neurological, endocrinological or other systemic diseases, as well as acute illness or chronic inflammatory or infective diseases, were excluded from the study. All the participants enrolled were of Chinese Han ethnicity. All the participants gave informed written consent to the study and did not take any medication known to affect glucose tolerance or insulin secretion before participation. The study was approved by the ethics committee of the Tongji Medical College. Concentrations of plasma TMAO were measured, and FMO3 E158K polymorphism (rs2266782) were genotyped.

Огноо

Сүүлд баталгаажуулсан: 03/31/2017
Эхлээд оруулсан: 04/23/2017
Тооцоолсон элсэлтийг оруулсан: 04/24/2017
Эхлээд нийтэлсэн: 04/26/2017
Сүүлийн шинэчлэлтийг оруулсан: 04/24/2017
Сүүлийн шинэчлэлтийг нийтэлсэн: 04/26/2017
Сургалтын бодит эхлэх огноо: 12/31/2011
Тооцоолсон анхан шатны ажил дуусах огноо: 12/29/2014
Судалгааны ажлыг дуусгах өдөр: 06/29/2016

Нөхцөл байдал эсвэл өвчин

Type2 Diabetes

Хөндлөнгийн оролцоо / эмчилгээ

Other: Plasma TMAO concentration

Үе шат

-

Arm Groups

ГарХөндлөнгийн оролцоо / эмчилгээ
Healthy control
A FPG concentration < 6.1 mmol/l, and a 2-h oral glucose tolerance test (OGTT) plasma glucose concentration < 7.8 mmol/l was considered normal glucose tolerance.
Type 2 diabetes
Type 2 diabetes was diagnosed when fasting plasma glucose (FPG) ≥ 7.0 mmol/l, and/or 2-h post-glucose load ≥ 11.1 mmol/l.

Эрхийн шалгуур

Суралцах боломжтой нас 30 Years Хэнд 30 Years
Суралцах боломжтой хүйсAll
Дээж авах аргаProbability Sample
Эрүүл сайн дурын ажилтнуудыг хүлээн авдагТийм ээ
Шалгуур үзүүлэлтүүд

Inclusion Criteria:

- Concomitantly, we recruited healthy individuals who were frequency-matched by age (±5 years) and sex to patients from an unselected population undergoing a routine health check-up in the same hospital.

- The inclusion criteria for controls and newly diagnosed type 2 diabetes were: age ≥ 30 years, body mass index (BMI) < 40 kg/m2, no history of a diagnosis of diabetes and no history of receiving pharmacological treatment for hyperlipidaemia or hypertension.

Exclusion Criteria:

- Patients with clinically significant neurological, endocrinological or other systemic diseases, as well as acute illness or chronic inflammatory or infective diseases, were excluded from the study.

Үр дүн

Анхан шатны үр дүнгийн арга хэмжээ

1. type 2 diabetes [through recruitment completion, an average of 3 years]

odd ratio (OR) for type 2 diabetes

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