Abstract
Aims:
To investigate the risk of macro- and microvascular complications in patients with
type 2 diabetes receiving rapid-acting insulin analogues (IA) or human regular insulin
(HI).
Methods:
General practice diabetes patients with continuous prescription of any IA or HI for
≥3 years were selected from the German Disease Analyzer database (IMS Health). Logistic
and Cox regression models were applied to analyze the incidence and time to onset
of vascular outcomes (IA vs. HI).
Results:
2764 patients on IA (insulin lispro, glulisine, aspart) and 4193 patients on HI were
included (age, mean [SD]: 61.0 [11.3] and 64.7 [10.5] years, follow-up [Q1,Q3]: 4.6
[3.7,6.1] and 4.7 [3.7,5.9] years). No significant differences were detected between
IA and HI regarding the incidence of vascular complications (OR [95%CI]: macrovascular
0.92 [0.72–1.18], microvascular 0.95 [0.77–1.17]) or regarding time to their onset,
after adjustment for sex, age, comorbidities and time on IA/HI, or by propensity-score-based
matching. However, in an additional short-term analysis (median [Q1,Q3] follow-up
(IA 2.9 [1.2,4.6], HI 2.4 [0.8,4.4] years) of a larger sample (no continuous insulin
treatment required) with more comorbidities, time to onset of macrovascular complications
was significantly longer for AI than HI (HR 0.88 [0.81–0.97], p=0.009; microvascular
complications: no difference).
Conclusions:
After long-term continuous treatment with IA or HI under real-life conditions, there
was no different risk of macro- or microvascular complications, contradicting previous
short-term analyses. Further prospective studies are needed to clarify whether selection
bias may have been introduced by using strict entry criteria.
Key words diabetes - cardiovascular risk management - insulin