Diabetic Ketoacidosis Severity at Diagnosis and Glycaemic Control in the First Year of Childhood Onset Type 1 DiabetesA Longitudinal Cohort Study

被引:9
作者
Khanolkar, Amal R. [1 ,2 ]
Amin, Rakesh [1 ]
Taylor-Robinson, David [3 ]
Viner, Russell M. [1 ]
Warner, Justin [4 ]
Gevers, Evelien F. [5 ,6 ]
Stephenson, Terence [1 ]
机构
[1] UCL, GOS Inst Child Hlth, 30 Guildford St, London WC1 1EH, England
[2] Karolinska Inst, Inst Environm Med, S-17177 Stockholm, Sweden
[3] Univ Liverpool, Dept Publ Hlth & Policy, Liverpool L69 3BX, Merseyside, England
[4] Childrens Hosp Wales, Dept Child Hlth, Cardiff CF14 4XW, S Glam, Wales
[5] Queen Mary Univ London, William Harvey Res Inst, Ctr Endocrinol, London EV1M 6BQ, England
[6] Barts Hlth NHS Trust Royal London Childrens Hosp, Dept Paediat Endocrinol, London E1 1BB, England
关键词
type; 1; diabetes; diabetic ketoacidosis; glycaemic control; ethnicity; inequalities; longitudinal analysis; METABOLIC-CONTROL; INSULIN INTENSIFICATION; CHILDREN; ADOLESCENTS; MELLITUS; AGE; COMPLICATIONS; TRAJECTORIES; DISEASE; GENDER;
D O I
10.3390/ijerph15010026
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
It is unclear whether diabetic ketoacidosis (DKA) severity at diagnosis affects the natural history of type 1 diabetes (T1D). We analysed associations between DKA severity at diagnosis and glycaemic control during the first year post-diagnosis. We followed 341 children with T1D, <19 years (64% non-white) attending paediatric diabetes clinics in East London. Data were extracted from routine medical registers. Subjects were categorized with normal, mild, moderate, or severe DKA. Linear mixed-effects modelling was used to assess differences in longitudinal HbA1(c) trajectories (glycaemic control) during 12 months post-diagnosis (1288 HbA1(c) data-points) based on DKA, adjusting for sex, age, ethnicity, SES (Socioeconomic Status) and treatment type. Females (OR 1.6, 95% CI 1.1-2.4) and younger age, 0-6 vs. 13-18 years (OR 2.9, 95% CI 1.5-5.6) had increased risk for DKA at diagnosis. Moderate or severe DKA was associated with higher HbA1(c) at diagnosis (adjusted estimates 8 mmol/mol, 2-14, and 10 mmol/mol, 4-15, respectively, compared to normal DKA). Differences in HbA1(c) trajectories by DKA were no longer apparent at six months post-diagnosis. All subjects experienced a steep decrease in HbA1(c) during the first three months followed by a gradual increase. While, DKA severity was not associated with glycaemic control at 12 months post-diagnosis, age at diagnosis, ethnicity, gender, and treatment type were significantly associated. For example, Black and mixed ethnicity children had increased risk for poor glycaemic control compared to White children (adjusted RRR 5.4, 95% CI 1.7-17.3 and RRR 2.5, 95% CI 1.2-6.0, respectively). DKA severity at diagnosis is associated with higher initial HbA1(c) but not glycaemic control from six months post-diagnosis. Age at diagnosis, ethnicity, gender, and insulin pump are associated with glycaemic control at one year post-diagnosis.
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页数:14
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