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SA JOURNAL OF DIABETES & VASCULAR DISEASE

RESEARCH ARTICLE

VOLUME 16 NUMBER 2 • NOVEMBER 2019

55

with and without hypothyroidism. It was done in a single-physician

practice in South Africa in a predominantly white population, and

results must be interpreted in this context.

The major findings of the study were the following: hypothyroid

subjects were significantly more likely to be female, older, with a

longer duration of diabetes and less likely to be black; diabetic

control, defined by HbA

1c

level, was better in hypothyroid subjects

than in the controls despite less use of hypoglycaemic agents;

hypothyroid subjects had higher HDL cholesterol and lower

triglyceride levels; lower eGFR and greater prevalence of CKD; there

was a trend to increased DR with no differences in amputations or

DPN; and a trend to increased CV events. However after adjustment

for baseline differences, the association of hypothyroidism with

DKD and DR was no longer apparent using multivariate analysis.

However the trend for CVD remained.

Table 4.

Associations between DKD and patient characteristics on uni-

and multivariate analysis

Univariate

Multivariate

Variable

OR (95% CI)

p

-value OR (95% CI)

p

-value

Age, 5-year increase 1.57 (1.37–1.79) < 0.001 1.63 (1.39–1.91) < 0.001

Gender, female

1.05 (0.64–1.72) 0.854 0.77 (0.43–1.38) 0.382

Race, non-black

1.16 (0.58–2.33) 0.668 0.67 (0.30–1.48) 0.322

Hypothyroid

1.74 (1.06–2.88) 0.029 1.25 (0.68–2.29) 0.467

HBA

1c

0.91 (0.32–2.58) 0.854 2.07 (0.60–7.19) 0.250

Duration of T2DM

1.60 (1.14–2.24) 0.007 0.90 (0.60–1.33) 0.592

Table 5.

Associations between DPN and patient characteristics on uni-

and multivariate analysis

Univariate

Multivariate

Variable

OR (95% CI)

p

-value OR (95% CI)

p

-value

Age, 5-year increase 1.21 (1.10–1.34) < 0.001 1.19 (1.05–1.35) 0.008

Gender, female

1.10 (0.70–1.71) 0.698 1.07 (0.65–1.77) 0.789

Race, non-black

2.11 (1.11–4.02) 0.023 1.66 (0.83–3.31) 0.152

Hypothyroid

0.92 (0.59–1.43) 0.706 0.63 (0.37–1.08) 0.094

CKD present

1.76 (1.06–2.90) 0.028 1.22 (0.70–2.16) 0.486

HBA

1c

1.37 (0.54–3.52) 0.507 1.47 (0.51–4.23) 0.480

Duration of DM

1.63 (1.21–2.20) 0.001 1.37 (0.97–1.93) 0.075

Table 6.

Associations between DR and patient characteristics on uni-

and multivariate analysis

Univariate

Multivariate

(

n

= 75)

(

n

= 75)

Variable

OR (95% CI)

p

-value OR (95% CI)

p

-value

Age, 5-year increase 1.26 (1.02–1.54) 0.029 1.19 (0.89–1.60) 0.235

Hypothyroid

2.2 (0.86–5.65) 0.102 1.61 (0.55–4.68) 0.386

CKD present

1.59 (0.62–4.06) 0.334 0.89 (0.29–2.75) 0.838

HBA

1c

5.67 (0.64–50.13) 0.118 6.52 (0.56–75.22) 0.133

Duration of DM

1.98 (0.97–4.07) 0.061 1.24 (0.52–2.99) 0.624

Table 7.

Associations between CVD and patient characteristics on uni-

and multivariate analysis

Univariate

Multivariate

(

n

= 75)

(

n

= 75)

Variable

OR (95% CI)

p

-value OR (95% CI)

p

-value

Age, 5-year increase 1.35 (1.18–1.56) < 0.001 1.41 (1.17–1.70) < 0.001

Gender, female

0.25 (0.13–0.48) < 0.001 0.16 (0.07–0.36) < 0.001

Race, non-black

1.10 (0.48–2.49) 0.826 0.63 (0.24–1.62) 0.336

Obese

0.74 (0.39–1.42) 0.371 0.87 (0.41–1.84) 0.713

Hypothyroid

1.76 (0.97–3.19) 0.064 1.97 (0.94–4.13) 0.073

HBA

1c

0.90 (0.26–3.13) 0.872 1.48 (0.33–6.71) 0.613

HDL-C

0.43 (0.15–1.27) 0.127 0.63 (0.18–2.23) 0.472

Duration of T2DM

1.70 (1.11–2.60) 0.014 1.19 (0.71–2.01) 0.512

1 mmol/l,

p

= 0.001) and triglyceride levels were significantly lower

(1.9 vs 2.1 mmol/l,

p

= 0.034). There was no difference in low-

density lipoprotein (LDL) cholesterol, but all subjects received statin

therapy unless contra-indicated.

Microvascular complications tended to occur more frequently

in the hypothyroid group. The eGFR was significantly lower in the

cases (66 vs 75 ml/min,

p

= 0.001), but there was no difference

in urine ACR. On univariate analysis (Table 3), the odds ratio for

DKD was 1.74 (

p

= 0.029), DPN was 0.92 (

p

= 0.7) and DR was

2.2 (

p

= 0.1). Because of baseline differences between the groups,

a multivariate analysis was performed to adjust for confounders

(Tables 4–6). The differences between the groups were no

longer significant. The most important predictor of microvascular

complications was a five-year increase in age, especially for DKD

(OR 1.63,

p

< 0.001) and DPN (OR 1.19,

p

= 0.008).

There was a trend towards a higher incidence of CVD in the

hypothyroid group (OR 1.76, p = 0.06) that was still present in

the multivariate analysis (OR 1.97,

p

= 0.07) (Table 7). The most

important predictor of CVD was age, and female gender appeared

protective. Amputations due to diabetes were 3.1% in the controls

and 3.0% in the cases (

p

= 0.725)

Discussion

This was a cross-sectional, retrospective study comparing primarily

micro- and macrovascular complications in type 2 diabetes subjects

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