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DOI 10.1007/s00059-013-3874-3

Медицинская библиотека · Herz · 2013

Noninvasive assessment of subclinical atherosclerosis in normotensive gravidae with gestational diabetes.

Atay A E, Simsek H, Demir B, Sakar M N, Kaya M, Pasa S, Demir S, Sit D

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Аннотация

AIM: Carotid artery intima-media thickness (CIMT), hyperhomocysteinemia, microalbuminuria, and nitric oxide reflect subclinical atherosclerosis and predict the risk of future cardiovascular events. We aimed to evaluate the presence of subclinical atherosclerosis and endothelial dysfunction in normotensive patients with gestational diabetes mellitus (GDM) noninvasively.

PATIENTS AND

METHODS

We enrolled 41 normotensive patients with GDM and 44 healthy gravidae in the study. Serum homocysteine and nitric oxide levels, urinary albumin excretion (microalbuminuria), and CIMT were evaluated along with lipid parameters and anthropometric measurements.

RESULTS

Patients with GDM had significantly higher levels of serum homocysteine, urinary albumin excretion, and increased CIMT (p < 0.001, p=0.005, and p < 0.001, respectively). Nitric oxide levels were significantly reduced in the patient group (p < 0.001). There was a significant difference between groups in terms of low-density lipoprotein (LDL) but not of high-density lipoprotein (HDL) and triglyceride levels. A significant correlation was observed between CIMT and serum LDL, HDL, homocysteine, nitric oxide levels, and urinary albumin excretion. Microalbuminuria was significantly correlated with serum homocysteine levels (p=0.03) but not with nitric oxide.

CONCLUSION

Independent of elevated blood pressure, subclinical atherosclerosis and endothelial dysfunction exist in normotensive patients with GDM. Further studies with a large number of participants are required to clarify these data.

Для цитирования: Atay A E, Simsek H, Demir B, Sakar M N, Kaya M, Pasa S, Demir S, Sit D. Noninvasive assessment of subclinical atherosclerosis in normotensive gravidae with gestational diabetes.. Herz. 2013. DOI: 10.1007/s00059-013-3874-3.

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