Cardiovascular Disease in Diabetes and Chronic Kidney Disease
被引:12
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作者:
Swamy, Sowmya
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George Washington Univ, Sch Med, Dept Med, Washington, DC 20052 USAGeorge Washington Univ, Sch Med, Dept Med, Washington, DC 20052 USA
Swamy, Sowmya
[1
]
Noor, Sahibzadi Mahrukh
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Loma Linda Univ, Sch Med, Dept Med, Loma Linda, CA 92350 USAGeorge Washington Univ, Sch Med, Dept Med, Washington, DC 20052 USA
Noor, Sahibzadi Mahrukh
[2
]
Mathew, Roy O.
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Loma Linda Univ, Sch Med, Dept Med, Loma Linda, CA 92350 USA
Loma Linda VA Healthcare Syst, Dept Med, 11201 Benton St, Loma Linda, CA 92357 USAGeorge Washington Univ, Sch Med, Dept Med, Washington, DC 20052 USA
Mathew, Roy O.
[2
,3
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机构:
[1] George Washington Univ, Sch Med, Dept Med, Washington, DC 20052 USA
[2] Loma Linda Univ, Sch Med, Dept Med, Loma Linda, CA 92350 USA
[3] Loma Linda VA Healthcare Syst, Dept Med, 11201 Benton St, Loma Linda, CA 92357 USA
Chronic kidney disease (CKD) is a common occurrence in patients with diabetes mellitus (DM), occurring in approximately 40% of cases. DM is also an important risk factor for cardiovascular disease (CVD), but CKD is an important mediator of this risk. Multiple CVD outcomes trials have revealed a greater risk for CVD events in patients with diabetes with CKD versus those without. Thus, reducing the risk of CKD in diabetes should result in improved CVD outcomes. To date, of blood pressure (BP) control, glycemic control, and inhibition of the renin-angiotensin system (RASI), glycemic control appears to have the best evidence for preventing CKD development. In established CKD, especially with albuminuria, RASI slows the progression of CKD. More recently, sodium glucose cotransporter 2 inhibitors (SGLT2i) and glucagon-like peptide receptor agonists (GLP1RA) have revolutionized the care of patients with diabetes with and without CKD. SGLT2i and GLP1RA have proven to reduce mortality, heart failure (HF) hospitalizations, and worsening CKD in patients with diabetes with and without existing CKD. The future of limiting CVD in diabetes and CKD is promising, and more evidence is forthcoming regarding combinations of evidence-based therapies to further minimize CVD events.
机构:
Manchester Royal Infirm, Manchester Inst Nephrol & Transplantat, Manchester, Lancs, EnglandManchester Royal Infirm, Manchester Inst Nephrol & Transplantat, Manchester, Lancs, England
Wright, Julian
Hutchison, Alastair
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Manchester Royal Infirm, Manchester Inst Nephrol & Transplantat, Manchester, Lancs, EnglandManchester Royal Infirm, Manchester Inst Nephrol & Transplantat, Manchester, Lancs, England
机构:
Auckland City Hosp, Dept Renal Med, Auckland, New Zealand
Univ Auckland, Dept Med, Auckland, New ZealandAuckland City Hosp, Dept Renal Med, Auckland, New Zealand
Pilmore, Helen
Dogra, Gursharan
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机构:
Sir Charles Gairdner Hosp, Dept Renal Med, Perth, WA, AustraliaAuckland City Hosp, Dept Renal Med, Auckland, New Zealand
Dogra, Gursharan
Roberts, Matthew
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机构:
Austin Hlth, Dept Nephrol, Melbourne, Vic, Australia
Univ Melbourne, Dept Med, Melbourne, Vic, AustraliaAuckland City Hosp, Dept Renal Med, Auckland, New Zealand
Roberts, Matthew
Heerspink, Hiddo J. Lambers
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机构:
Univ Groningen, Univ Med Ctr Groningen, Dept Clin Pharmacol, Groningen, NetherlandsAuckland City Hosp, Dept Renal Med, Auckland, New Zealand
Heerspink, Hiddo J. Lambers
Ninomiya, Toshiharu
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机构:
Kyushu Univ Hosp, Dept Nephrol Hypertens & Strokol, Kyushu, JapanAuckland City Hosp, Dept Renal Med, Auckland, New Zealand
Ninomiya, Toshiharu
Huxley, Rachel
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机构:
Univ Sydney, George Inst Global Hlth, Sydney, NSW 2006, AustraliaAuckland City Hosp, Dept Renal Med, Auckland, New Zealand
机构:
Childrens Hosp, Med Ctr, Div Nephrol & Hypertens, Cincinnati, OH 45229 USAChildrens Hosp, Med Ctr, Div Nephrol & Hypertens, Cincinnati, OH 45229 USA