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Oral Presentations

Epidemiology and Prevention of Diabetes

OL01-2

Characteristics of abnormal oral glucose tolerance test in GDM

diagnosis

Dittakarn BORIBOONHIRUNSARN

1

*.

1

Faculty of Medicine Siriraj

Hospital, Mahidol University, Thailand

Objectives:

To describe characteristics of abnormal OGTT

values in GDM diagnosis and their clinical correlation. In

addition, the effects of omitting any OGTT value on GDM

diagnosis were evaluated.

Methods:

A total of 415 women diagnosed with GDM were

included. GDM screening and diagnosis results were extracted

from medical records. Detailed analysis of OGTT values at the

time of GDMdiagnosis was performed, including prevalence of

abnormalities of each value, number of abnormal values. In

addition, relationship between abnormal OGTT values and

maternal characteristics and clinical characteristics were also

evaluated.

Results:

Mean age was 32.9 years, 46% were nulliparous, and

39% were overweight. Mean gestational age at diagnosis was

19.2 weeks and 42.4% were diagnosed during 24

28 weeks.

Insulin therapy was indicated in 12% of cases. Most common

abnormalities were found in the 2nd and 3rd values (85.3%

and 96.6% respectively). In terms of number of abnormal

OGTT values, abnormal 2 values was found in 42.9% while

abnormal 3 or 4 values were found in 34.2% and 22.9%,

respectively. Detailed analysis revealed that 16.7% of GDM

would be missed if the 4th OGTT was omitted, including 2

cases who required insulin therapy. Number of abnormal

OGTT values were significantly higher among overweight

women (p = 0.02) and those who required insulin therapy

(p < 0.001), but not related to timing of diagnosis. Mean birth

weight and rate of macrosomia were also comparable between

different numbers of abnormal OGTT values.

Conclusion:

Among GDM women, 57.1% had abnormal 3 or 4

OGTT values. Number of abnormal OGTT values were posi-

tively related to overweight and insulin requirement. Omitting

the 4th OGTT value would result in unacceptable 16.7%

undiagnosed GDM.

OL01-3

Increased risk for diabetes development in subjects with large

variation in total cholesterol levels in Koreans

Eun-Jung RHEE

1

*, Kyungdo HAN

2

, Seung-Hyun KO

3

,

Kyung Soo KO

4

, Ki-Up LEE

5

, Won-Young LEE

1

.

1

Department of

Endocrinology and Metabolism, Kangbuk Samsung Hospital,

Sungkyunkwan University School of Medicine,

2

Department of

Medical Statistics, College of Medicine, The Catholic University of

Korea,

3

Divisin of Endocrinology and Metabolism, Department of

Internal Medicine, St. Vincent

s Hospital, College of Medicine, The

Catholic University of Korea,

4

Department of Internal Medicine,

Cardiovascular and Metabolic Disease Center, Inje University

Sanggye Paik Hospital, Inje University College of Medicine,

5

Department of Internal Medicine, Asan Medical Center, University of

Ulsan College of Medicine, Korea

Background:

Recent studies suggest the role of hyperlipidemia

on development of diabetes. However, statins are reported to

increase the risk for diabetes development. We analyzed the

relationship between the variations of total cholesterol (TC)

levels and the risk of type 2 diabetes in data from a Korean

nationwide population-based study.

Methods:

In 2,827,950 Korea examinees in general health

check-up database (DB) as a sub-dataset of Korean National

Health Insurance Service (NHIS), in whom at least two health

check-up data were available between 2002 and 2006, and did

not have diabetes at baseline, the variations of TC between the

examinations were calculated. The examinees were divided

into 10 groups according to deciles of TC variation and the

hazard ratio for diabetes development from 2007 to 2013 were

analyzed.

Results:

During the follow-up period, 3.4% of the examinees

developed diabetes. The subjects with the highest decile of TC

variation (32.5%) showed the highest incidence rate for

diabetes among the decile groups of TC variation (5.24%), and

the incidence rate for diabetes showed J-shaped curve with

fourth decile group showed the lowest incidence rate for

diabetes. The highest decile group of TC variation showed

increased hazard ratio for diabetes development after adjust-

ment for confounding variables (1.16; 95% CI 1.14

1.18). These

results were similarly observed in either group with or without

hyperlipidemic medication.

Conclusions:

The subjects with large variation of TC showed

increased risk for diabetes development, independent to the

medicationof hyperlipidemic agents. These results suggest the

possibilityof contribution of variation inTC level, not themedi-

cation itself that affects the risk for diabetes development.

OL01-4

Central blood pressure and insulin sensitivity after an oral

glucose loading

Ang-Tse LEE

1

, Chia-Lin LEE

1,2,4

, I-Te LEE

1,7

, Jun-Sing WANG

1,8

,

Chen-Chi WANG

3

, Shih-An LIU

3

, Wen-Jane LEE

4

,

Shih-Yi LIN

1,5,7

, Chen-Huan CHEN

6,7,9

, Wayne H-H SHEU

1,7,10

*.

1

Division of Endocrinology and Metabolism, Department of Internal

Medicine, Taichung Veterans General Hospital,

2

Department of Public

Health, College of Public Health, China Medical University,

3

Department of Otolaryngology, Taichung Veterans General Hospital,

4

Department of Medical Research, Taichung Veterans General

Hospital,

5

Center for Geriatrics and Gerontology, Taichung Veterans

General Hospital, Taichung,

6

Department of Medicine, Taipei

Veterans General Hospital,

7

School of Medicine, National Yang-Ming

University,

8

Institute of Clinical Medicine, School of Medicine,

National Yang-Ming University,

9

Institute of Public Health, National

Yang-Ming University,

10

College of Medicine, National Defense

Medical Center, Taipei, Taiwan

Background:

Although peripheral blood pressure (BP) is

generally used to guide therapeutic decisions, recent

D IABETES R ESEARCH AND C LINICAL P RACTICE 120S1 (2016) S40 S64

Contents available at

ScienceDirect

Diabetes Research

and Clinical Practice

journal homepage:

www.elsevier.com/locate/diabres

0168-8227© 2016 Elsevier Ireland Ltd. All rights reserved.