Glycaemic control and microvascular
complication among patients with youth onset diabetes in India
using differing types of insulin and methods of glucose monitoring.
Diabetes Research and Clinical
Practice, 2004 (Article in Press)
Abstract
We assessed Whether
insulin types and monitoring methods were relevant to glycaemic
control, microvascular complications as well as costs of management
in 208 patients with youth onset diabetes in India. The type
of insulin and monitoring method used made no difference to
the glycaemic and complication status. Cost considerations
support bovine insulin use along with urine glucose monitoring
as an appropriate approach to diabetes self care in developing
couniries.
2004 published by Elsevier Ireland 1.1d.
Keywords: Glucose monitoring;
Types of insulin; Glycaernic control
Insulin requiring youth onset
diabetes mellitus' in India includes patients with type I
diabetes (38%), ketosis resistant type (32%) and fibrocalculous
pancreatopathy (10%) [1,2]. The majority (60%) of them are
poor and prefer urine glucose monitoring and bovine insulin.
DCCT has shown the advantages of tight glycaenlic control
(3], although the ellicacy of SHBG in reducing glycosylated
Hb has been questioned [4].
We assessed die relative
efficacy of different methods of management in 208 insulin
requiring patients attending 'diabetes clinic of young' at
AllMS, Delhi, during 1990-2002 (M:F, 87:121; mean age ±
S.D., 27.3 ± 9.1 years; duration of follow up, 6.4
± 2.9 years). Patients aged less than 8 years, or with
recent infections or pregnancy were excluded. Thcre were four
study groups as followed: group 1, patients on hurnan insulin
and using SHBG; group 2, bovine insulin and SHBG; group 3,
bovine insulin and urine glucose monitoring; group 4, any
type of insulin with no monitoring.
The type Of insulin therapy
and glucose monitoring method adoptcd were based on choice
and ' affordability. Patients were followed up at two months
intervals for insulin suppily and care. Benedict's method
or commercially available strips were used to monitor urine
glucose at least once a day. The knowledge on insulin injection,
hypoglycaemia awareness and dietary precautions were assessed
in a subset of 52 patients using a questionnaire [5]. The
mean of the last three HbA I values (normal range, 6.5-8%)
was used to assess glycaemic control status. A 24th urinary
protein between 51 and 499mg indicated microproteinuria and
the values >500 mg was regarded as macroproteinuria [6].
Data is shown as mean ±
S.D. (Table 1). The mean duration of diabetes, BMI., HbA I
values at the tirne of first presentation, their follow up
period in the clinic, daily insulin dose requireiment and
mean diabetes education score were not significantly different(ANOVA)
among the Four groups. All the four groups showed improvement
in the mean BMI and HbAl values after a mean follow up period
of 6 years. However, the mean delta HbAI and frequency or
microproteinuria or macroproteinuria were not different between
groups. Number of subjects with HbAI>9.0% was not significantly
different in groups 1, 2 and 3. there was an inverse relation
between final HbAI values and the diabetes knowledge score
(r=-0.146, p=0.21) The monthly expenditure on the management
of diabetes by each patient was Rs.1440($ 30.6), 990 ($21),
360($7.6) in groups 1,2 and 3 respectively. the cost of SHBG
was 32 fold higher than urine glucose monitoring.
There is paucity of information
from developing countries regarding the efficacy of different
types of insulin and monitoring methods based on long term
glycamic control and complications like nephropathy. Despite
the prohibitive cost of the therapy, poor patient education
and poor preservation of glucose monitoring strips the mean
HbAI levels observed in the present study were comparable
to that reported from diabetic clinics of developed countries
[7-9]. In consideration of the relative cost of the different
methods of management used, it can be concluded that urine
glucose monitoring and bovine insulin therapy may be appropriate
for many patients with type I diabetes mellitus in India.
Table 1
Clinical characteristics of the study groups using different
methods of treatment and monitoring
 |
| Parameters |
Human insulin and blood glucose
monitoring |
Bovine insulin and blood glucose
monitoring |
Bovine insulin and urine glucose
monitoring |
No self monitoring
|
P-value |
| |
(group 1) |
(group 2) |
(group 3) |
(group 4) |
|
 |
| N |
46 |
65 |
60 |
37 |
|
| Age (year) |
23.3± 9.7 |
29.7 ± 9,4 |
28.9 ± SA |
25.6 ± 7.8 |
group 1< group 2 and group
3 |
| Duration of diabetes (year) |
10.6 ± 74 (46) |
12.9 ± 6.6 (65) |
11.7 ± 5.6 (60) |
9.9 ± 5.8 |
N S |
| Duration of follow-up (year) |
6.6 ± 2.8 (37) |
5.5 ± 2.8 (46) |
6.7 ± 29 (65) |
6.5 ± 2.9 (60) |
NS |
| Diabetes education score |
31.8± 2.6 (11) |
31.2 ± 2.9 (31) |
29.1± 3.8 (3.1) |
32.7 ± 3.2(4) |
NS |
| BMI, basal (kg/m2) |
I9.3 ± 3.8 (44) |
19.0 ± 4.2 (64) |
18.7 ± 1.6 (55) |
18.9 ± 4.6 |
NS |
| BMI, post follow-up (kg/m2) |
20.6± 4.7 (41) |
20.6 ± 3.9 (60) |
20.0 ± 3.4 (50) |
20.9 ± 4.0(34) |
NS |
| Daily insulin dose used (IU) |
33.8 ± 12.8 (36) |
36.9 ± 13.4 (53) |
39.8 ± 13.6 (46) |
31.8 ± 13.4(34) |
NS |
| HbAl basal (%) |
12.1±12.8 (45) |
12.5±3.0 (64) |
12.8±3.2 (58) |
13.8 ± 3.2 |
NS |
| HbAl post follow-up |
10.6 2.3 (45) |
11.2 ± 2.1 (63) |
12.0 ± 2.9 (55) |
12.04 ± 2.8(37) |
group I vs group 3 and group
4
|
| Delta HbA I |
1.5±3.1 (47) |
1.31±3(62) |
0. 84±4(54) |
1.7 ± 2.9 (37) |
NS |
| Subjects with HbAl <9% |
9/45 (20%) |
11/63 (17.5%) |
9/55 (16.5%) |
5/37(13.5%) |
NS |
| Microproteinuria |
22.31 (71.0%) |
34/54(63.0%) |
21/38 (55.3%) |
22/30(73.3%) |
NS |
| Macroproteinuria |
9.7(31) |
13.0 (54) |
23.7 (38) |
(30) |
|
| Insulin cost per month in Rs. |
630(A) |
180(3.8) |
ISO(3.8) |
|
|
| (USS) |
|
|
|
|
|
| Monitoring cost per month m |
660(14.0) |
660(14.0) |
30 (0~6) |
|
|
| Rs. (USS) |
|
|
|
|
|
| Net cost per month in diabetes |
1440 (3 0. 6) |
990 (21.0) |
360 (7.6) |
|
|
| management in Rs- (USS) |
|
|
|
|
|
| Data is shown as mean ± S.D. |
|
|
|
|
|
 |
©
2000 Elsevier Science Ireland Ltd. All rights reserved. With
permission from Elsevier Science Ireland Ltd.
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