TY - JOUR
T1 - The relationship between intensification of blood glucose-lowering therapies, health status and quality of life in type 2 diabetes
T2 - The Fremantle Diabetes Study Phase II
AU - Davis, Timothy M.E.
AU - Bruce, David G.
AU - Curtis, Bradley H.
AU - Barraclough, Helen
AU - Davis, Wendy A.
PY - 2018/8/1
Y1 - 2018/8/1
N2 - Aims: To determine whether therapeutic intensification in type 2 diabetes influences health status and quality of life (QoL). Methods: We studied 930 participants in the longitudinal observational Fremantle Diabetes Study Phase II (mean age 65.3 years, 53.8% males, median diabetes duration 8.0 years) with valid data from baseline assessment and two biennial reviews (4 years of follow-up) between 2008 and 2015. The main outcome measures were the Short Form-12 version 2 physical and mental health composite scores (PCS, MCS) and the average weighted impact (AWI) score from the Audit of Diabetes Dependent QoL. Results: There were reductions in PCS at Year 4 compared with baseline and Year 2 in patients on stable diet-based management (n = 160), oral glucose-lowering medication (OGLM; n = 387), and insulin with/without OGLM (n = 168; P < 0.05), but no statistically significant temporal changes in MCS/AWI. Insulin-treated patients had the lowest PCS, MCS and AWI compared to the other two subgroups at each time-point (P ≤ 0.012). In participants initiating OGLM (n = 84) or insulin (n = 85), there were no differences in PCS, MCS or AWI at the biennial assessments either side of these therapeutic changes (P ≥ 0.08). Conclusions: These real-life data show that treatment intensification, including insulin initiation, does not impact adversely on patient well-being in community-based type 2 diabetes. Since insulin use at entry was associated with longer diabetes duration, worse glycaemic control, and a greater risk of chronic complications, the burden of disease rather than treatment modality appears the primary determinant of health status and QoL.
AB - Aims: To determine whether therapeutic intensification in type 2 diabetes influences health status and quality of life (QoL). Methods: We studied 930 participants in the longitudinal observational Fremantle Diabetes Study Phase II (mean age 65.3 years, 53.8% males, median diabetes duration 8.0 years) with valid data from baseline assessment and two biennial reviews (4 years of follow-up) between 2008 and 2015. The main outcome measures were the Short Form-12 version 2 physical and mental health composite scores (PCS, MCS) and the average weighted impact (AWI) score from the Audit of Diabetes Dependent QoL. Results: There were reductions in PCS at Year 4 compared with baseline and Year 2 in patients on stable diet-based management (n = 160), oral glucose-lowering medication (OGLM; n = 387), and insulin with/without OGLM (n = 168; P < 0.05), but no statistically significant temporal changes in MCS/AWI. Insulin-treated patients had the lowest PCS, MCS and AWI compared to the other two subgroups at each time-point (P ≤ 0.012). In participants initiating OGLM (n = 84) or insulin (n = 85), there were no differences in PCS, MCS or AWI at the biennial assessments either side of these therapeutic changes (P ≥ 0.08). Conclusions: These real-life data show that treatment intensification, including insulin initiation, does not impact adversely on patient well-being in community-based type 2 diabetes. Since insulin use at entry was associated with longer diabetes duration, worse glycaemic control, and a greater risk of chronic complications, the burden of disease rather than treatment modality appears the primary determinant of health status and QoL.
KW - Health status
KW - Quality of life
KW - Treatment intensification
KW - Type 2 diabetes
UR - http://www.scopus.com/inward/record.url?scp=85048593757&partnerID=8YFLogxK
U2 - 10.1016/j.diabres.2018.05.047
DO - 10.1016/j.diabres.2018.05.047
M3 - Article
C2 - 29879496
AN - SCOPUS:85048593757
SN - 0168-8227
VL - 142
SP - 294
EP - 302
JO - Diabetes Research and Clinical Practice
JF - Diabetes Research and Clinical Practice
ER -