TY - JOUR
T1 - Role of Microalbuminuria in Predicting Cardiovascular Mortality in Individuals With Subclinical Hypothyroidism
AU - Tuliani, Tushar A.
AU - Shenoy, Maithili
AU - Belgrave, Kevin
AU - Deshmukh, Abhishek
AU - Pant, Sadip
AU - Hilliard, Anthony
AU - Afonso, Luis
PY - 2017/9/1
Y1 - 2017/9/1
N2 - Purpose Studies suggest that subclinical hypothyroidism (SCH) is related to cardiovascular mortality (CVM). We explored the role of microalbuminuria (MIA) as a predictor of long-term CVM in population with and without SCH with normal kidney function. Materials and Methods We examined the National Health and Nutrition Education Survey - III database (n = 6,812). Individuals younger than 40 years, thyroid-stimulating hormone levels ≥20 and ≤0.35 mIU/L, estimated glomerular filtration rate <60 mL/minute/1.73 m2 and urine albumin-to-creatinine ratio of >250 mg/g in men and >355 mg/g in women were excluded. SCH was defined as thyroid-stimulating hormone levels between 5 and 19.99 mIU/L and serum T4 levels between 5 and 12 µg/dL. MIA was defined as urine albumin-to-creatinine ratio of 17-250 mg/g in men and 25-355 mg/g in women. Patients were categorized into the following 4 groups: (1) no SCH or MIA, (2) MIA, but no SCH, (3) SCH, but no MIA and (4) both SCH and MIA. Results Prevalence of MIA in the subclinical hypothyroid cohort was 21% compared to 16.4% in those without SCH (P = 0.03). SCH was a significant independent predictor of MIA (n = 6,812), after adjusting for traditional risk factors (unadjusted odds ratio = 1.75; 95% CI: 1.24-2.48; P = 0.002 and adjusted odds ratio = 1.83; 95% CI: 1.2-2.79; P = 0.006). MIA was a significant independent predictor of long-term all-cause (adjusted hazard ratio = 1.7, 95% CI: 1.24-2.33) and CVM (adjusted hazard ratio = 1.72, 95% CI: 1.07-2.76) in subclinical hypothyroid individuals. Conclusions In a cohort of subclinical hypothyroid individuals, the presence of MIA predicts increased risk of CVM as compared to nonmicroalbuminurics with SCH. Further randomized trials are needed to assess the benefits of treating microalbuminuric subclinical hypothyroid individuals and impact on CVM.
AB - Purpose Studies suggest that subclinical hypothyroidism (SCH) is related to cardiovascular mortality (CVM). We explored the role of microalbuminuria (MIA) as a predictor of long-term CVM in population with and without SCH with normal kidney function. Materials and Methods We examined the National Health and Nutrition Education Survey - III database (n = 6,812). Individuals younger than 40 years, thyroid-stimulating hormone levels ≥20 and ≤0.35 mIU/L, estimated glomerular filtration rate <60 mL/minute/1.73 m2 and urine albumin-to-creatinine ratio of >250 mg/g in men and >355 mg/g in women were excluded. SCH was defined as thyroid-stimulating hormone levels between 5 and 19.99 mIU/L and serum T4 levels between 5 and 12 µg/dL. MIA was defined as urine albumin-to-creatinine ratio of 17-250 mg/g in men and 25-355 mg/g in women. Patients were categorized into the following 4 groups: (1) no SCH or MIA, (2) MIA, but no SCH, (3) SCH, but no MIA and (4) both SCH and MIA. Results Prevalence of MIA in the subclinical hypothyroid cohort was 21% compared to 16.4% in those without SCH (P = 0.03). SCH was a significant independent predictor of MIA (n = 6,812), after adjusting for traditional risk factors (unadjusted odds ratio = 1.75; 95% CI: 1.24-2.48; P = 0.002 and adjusted odds ratio = 1.83; 95% CI: 1.2-2.79; P = 0.006). MIA was a significant independent predictor of long-term all-cause (adjusted hazard ratio = 1.7, 95% CI: 1.24-2.33) and CVM (adjusted hazard ratio = 1.72, 95% CI: 1.07-2.76) in subclinical hypothyroid individuals. Conclusions In a cohort of subclinical hypothyroid individuals, the presence of MIA predicts increased risk of CVM as compared to nonmicroalbuminurics with SCH. Further randomized trials are needed to assess the benefits of treating microalbuminuric subclinical hypothyroid individuals and impact on CVM.
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U2 - 10.1016/j.amjms.2017.04.022
DO - 10.1016/j.amjms.2017.04.022
M3 - Article
C2 - 28918836
AN - SCOPUS:85030438385
SN - 0002-9629
VL - 354
SP - 285
EP - 290
JO - American Journal of the Medical Sciences
JF - American Journal of the Medical Sciences
IS - 3
ER -