An evaluation of early cardiometabolic risk factors in children and adolescents with Turner syndrome. (6th April 2013)

• Record Type: Journal Article
• Authors: O'Gorman, Clodagh S.; Syme, Catriona; Lang, Jun; Bradley, Timothy J.; Wells, Greg D.; Hamilton, Jill K.
• Is Part Of: Clinical endocrinology. Volume 78:Number 6(2013:Jun.)
• Page Start: 907
• Page End: 913
• Publication Date: 2013-04-06
• Subjects: Endocrinology -- Periodicals; 616.4005
• DOI: 10.1111/cen.12079
• Languages: English
• ISSNs: 0300-0664

Abstract

<abstract abstract-type="main" id="cen12079-abs-0001"> <title>Summary</title> <sec id="cen12079-sec-0001" sec-type="section"> <title>Background and Objectives</title> <p>Turner syndrome (TS) confers increased lifetime risk of type 2 diabetes mellitus and cardiovascular disease. We compared cardiometabolic risk factors and measures of subcutaneous, visceral adipose tissue and intra‐myocellular lipid between young TS girls and an age‐ and BMI‐standard deviation scores (SDS)‐matched healthy female cohort.</p> </sec> <sec id="cen12079-sec-0002" sec-type="section"> <title>Patients and <sc>M</sc>ethods</title> <p>A cross‐sectional cohort study was conducted at the Hospital for Sick Children, Toronto. Nineteen TS and 17 control girls (13·7 ± 2·5 <italic>vs</italic> 12·7 ± 3·4 years of age, respectively, <italic>P</italic> = 0·30). Multiple‐sample oral glucose tolerance test with measurement of fasting insulin, LDL, HDL, triglycerides, adiponectin and highly sensitive C‐reactive protein (hsCRP) was performed. Subcutaneous adipose tissue, visceral adipose tissue intramyocellular lipid levels evaluated by magnetic resonance techniques. Insulin secretion (IS), sensitivity (Si) and the insulin secretion–sensitivity index (ISSI‐2) were calculated from oral glucose tolerance test data.</p> </sec> <sec id="cen12079-sec-0003" sec-type="section"> <title>Results</title> <p>Five TS and no controls had impaired fasting glucose or impaired glucose tolerance; none had type 2 diabetes mellitus. Insulin sensitivity and insulin secretion were similar between groups; ISSI‐2 was lower in TS (923·5 ± 307·3 <italic>vs</italic> 659·1 ± 387·3; <italic>P</italic> = 0·03). TS girls had higher blood pressure (82·5 ± 13·6 <italic>vs</italic> 73·5 ± 5·5 mmHg; <italic>P</italic> = 0·0146), waist circumference (76·0 ±11·8 <italic>vs</italic> 65·9 ± 9·7; <italic>P</italic> = 0·0087) and subcutaneous adipose tissue (135·6 ± 88·6 <italic>vs</italic> 69·3 ± 59·9; <italic>P</italic> = 0·01) than controls. Visceral adipose tissue, intramyocellular lipid levels and adiponectin were not different between groups. TS girls also had higher triglycerides (1·1 ± 0·6 <italic>vs</italic> 0·7 ± 0·3; <italic>P</italic> = 0·003), total cholesterol (4·4 ± 0·7 <italic>vs</italic> 3·9 ± 0·4; <italic>P</italic> = 0·02) and hsCRP (2·0 ± 1·9 <italic>vs</italic> 0·8 ± 0·3; <italic>P</italic> = 0·01).</p> </sec> <sec id="cen12079-sec-0004" sec-type="section"> <title> <sc>C</sc>onclusions</title> <p>TS girls exhibit more cardiometabolic risk factors and reduced beta cell function compared with age‐ and BMI‐SDS‐matched girls. Increased awareness of early risk of type 2 diabetes mellitus and hypertension in TS girls is needed.</p> </sec> </abstract>