PMID- 31601203 OWN - NLM STAT- MEDLINE DCOM- 20200312 LR - 20200312 IS - 1472-6823 (Electronic) IS - 1472-6823 (Linking) VI - 19 IP - 1 DP - 2019 Oct 11 TI - Prevalence of cardiovascular risk factors in non-menopausal and postmenopausal inpatients with type 2 diabetes mellitus in China. PG - 98 LID - 10.1186/s12902-019-0427-7 [doi] LID - 98 AB - BACKGROUND: To investigate the prevalence of cardiovascular disease (CVD) risk factors and assess the 10-year risk of CVD in non-menopausal and postmenopausal women with type 2 diabetes mellitus (T2DM). METHODS: A total of 569 patients with T2DM at a Chinese tertiary hospital were investigated using the Framingham Risk Score (FRS). We evaluated the 10-year risk of CVD, clinical and menopause characteristics in all subjects. RESULTS: Among the 569 diabetic patients, the incidence of smoking, dyslipidemia, hypertension, overweight or obesity, and nonalcoholic fatty liver disease (NAFLD) was 0.7, 36.2, 38.1 56.6 and 58.2%, respectively. The usage rate of hypoglycemic agents, antihypertensive agents, lipid modulators and antithrombotic drugs was 88.6, 78.3, 50.0 and 27.1%, respectively. However, only 1.2% of inpatients achieved the three target goals for the control of blood glucose (HbA(1c) < 7%), blood pressure (systolic blood pressure < 130 mmHg, diastolic blood pressure < 80 mmHg), and blood lipids (total cholesterol < 174 mg/dL). The 10-year risk of CVD was (1.6 +/- 1.5%) and tended to increase along with age (F = 27.726, P < 0.001). For all subjects (n = 569), multiple linear regression analysis showed that menopause (beta = 0.275, P < 0.001), low-density lipoprotein cholesterol (LDL-C) (beta = 0.212, P < 0.001), fasting plasma glucose (FPG) (beta = 0.093, P = 0.018) and waist-to-hip-ratio (beta = - 0.078, P = 0.047) were risk factors of 10-year risk of CVD, which may explain the variance of 14.3%. In the postmenopausal group (n = 397), LDL-C (beta = 0.227, P < 0.001), FPG (beta = 0.139, P = 0.003) and time since menopause (beta = 0.230, P < 0.001) were found to be associated with CVD, which may explain the variance of 14.6%. CONCLUSION: The incidence of dyslipidmia, hypertension, overweight or obesity and NAFLD is high. The level of control of blood glucose, blood pressure, and blood lipids was found to be extremely low and the treatment status was not ideal. Besides menopause, LDL-C, FPG and time since menopause were found to be independent risk factors for the 10-year risk of CVD. Therefore, it is necessary to focus on comprehensive control of multiple risk factors, such as plasma glucose, blood pressure and serum lipid. FAU - Zhou, Huanhuan AU - Zhou H AD - The First People's Hospital of Changzhou, 185# Juqian Road, Changzhou, 213000, Jiangsu Province, China. FAU - Zhang, Chenghuan AU - Zhang C AD - The First People's Hospital of Changzhou, 185# Juqian Road, Changzhou, 213000, Jiangsu Province, China. FAU - Ni, Jingyu AU - Ni J AD - The First People's Hospital of Changzhou, 185# Juqian Road, Changzhou, 213000, Jiangsu Province, China. FAU - Han, Xiaoyun AU - Han X AUID- ORCID: 0000-0002-6257-8540 AD - The First People's Hospital of Changzhou, 185# Juqian Road, Changzhou, 213000, Jiangsu Province, China. lanao163@sina.com. LA - eng PT - Journal Article DEP - 20191011 PL - England TA - BMC Endocr Disord JT - BMC endocrine disorders JID - 101088676 RN - 0 (Biomarkers) SB - IM MH - Adult MH - Biomarkers/analysis MH - Cardiovascular Diseases/*epidemiology/*etiology/metabolism/pathology MH - China/epidemiology MH - Cross-Sectional Studies MH - Diabetes Mellitus, Type 2/*complications MH - Female MH - Follow-Up Studies MH - Humans MH - Middle Aged MH - *Postmenopause MH - *Premenopause MH - Prevalence MH - Prognosis MH - Risk Factors PMC - PMC6787985 OTO - NOTNLM OT - Cardiovascular disease OT - Diabetes mellitus OT - Framingham risk score OT - Menopause OT - Type 2 COIS- The authors declare that they have no competing interests. EDAT- 2019/10/12 06:00 MHDA- 2020/03/13 06:00 PMCR- 2019/10/11 CRDT- 2019/10/12 06:00 PHST- 2019/04/29 00:00 [received] PHST- 2019/09/13 00:00 [accepted] PHST- 2019/10/12 06:00 [entrez] PHST- 2019/10/12 06:00 [pubmed] PHST- 2020/03/13 06:00 [medline] PHST- 2019/10/11 00:00 [pmc-release] AID - 10.1186/s12902-019-0427-7 [pii] AID - 427 [pii] AID - 10.1186/s12902-019-0427-7 [doi] PST - epublish SO - BMC Endocr Disord. 2019 Oct 11;19(1):98. doi: 10.1186/s12902-019-0427-7.