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Eicosapentaenoic and Docosahexaenoic Acids Attenuate Progression of Albuminuria in Patients With Type 2 Diabetes Mellitus and Coronary Artery Disease

Elajami TK, Alfaddagh A, Lakshminarayan D, Soliman M, Chandnani M, Welty FK

Journal of the American Heart Association · 41 citas

Cómo se estudió

Diseño
Ensayo controlado aleatorizado (indexado por PubMed)
Estudiado en
Personas
Resultado principal
Marcadores de salud y funcionamiento

Quién lo pagó

Financiación
Posiblemente financiado por la industria

Según la declaración de financiación del texto completo.

Publicación

Publicado
2017-07-01 · J Am Heart Assoc · vol. 6 · número 7
Editorial
Wiley
Citado
51 citas · más que el 92% de estudios similares · 3.2× el promedio de su campo
Impacto
Entre el 10 % más citado de su campo
Referencias
70 trabajos
Acceso
Acceso abierto (revista) · CC-BY-NC-ND
Áreas de investigación
Fatty Acid Research and Health · Natural Products and Biological Research · Eicosanoids and Hypertension Pharmacology
Palabras clave
Medicine, Albuminuria, Internal medicine, Angiotensin receptor, Eicosapentaenoic acid, Diabetes mellitus, Endocrinology, Docosahexaenoic acid, Angiotensin-converting enzyme, Coronary artery disease, Type 2 Diabetes Mellitus, Creatinine, Angiotensin II, Blood pressure, Polyunsaturated fatty acid, Fatty acid
MeSH
humans, diabetic nephropathies, albuminuria, hypertension, diabetes mellitus, type 2, disease progression, docosahexaenoic acids, eicosapentaenoic acid, drug combinations, angiotensin ii type 1 receptor blockers, angiotensin-converting enzyme inhibitors, treatment outcome, risk factors, prospective studies, time factors, dietary supplements, adult, aged, aged, 80 and over, middle aged, boston, female, male, coronary artery disease

6 autores

  • Tarec K. Elajami🇺🇸Beth Israel Deaconess Medical Center; Harvard University
  • Abdulhamied Alfaddagh🇺🇸Beth Israel Deaconess Medical Center; Harvard University
  • Dharshan Lakshminarayan🇺🇸Beth Israel Deaconess Medical Center; Harvard University
  • Michael Y. Soliman🇺🇸Beth Israel Deaconess Medical Center; Harvard University
  • Madhuri Chandnani🇺🇸Beth Israel Deaconess Medical Center; Harvard University
  • Francine K. Welty🇺🇸Beth Israel Deaconess Medical Center; Harvard University

Resumen

El texto original del estudio, en el idioma en que se publicó.

Background

Albuminuria is a marker of inflammation and an independent predictor of cardiovascular morbidity and mortality. The current study evaluated whether eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) supplementation attenuates progression of albuminuria in subjects with coronary artery disease.

Methods and results

Two-hundred sixty-two subjects with stable coronary artery disease were randomized to either Lovaza (1.86 g of EPA and 1.5 g of DHA daily) or no Lovaza (control) for 1 year. Percent change in urine albumin-to-creatinine ratio (ACR) was compared. Mean (SD) age was 63.3 (7.6) years; 17% were women and 30% had type 2 diabetes mellitus. In nondiabetic subjects, no change in urine ACR occurred in either the Lovaza or control groups. In contrast, ACR increased 72.3% (PPr=0.394, P=0.01).

Conclusions

EPA and DHA supplementation attenuated progression of albuminuria in subjects with type 2 diabetes mellitus and coronary artery disease, most of whom were on an angiotensin-converting enzyme-inhibitor or angiotensin-receptor blocker. Thus, EPA and DHA supplementation should be considered as additional therapy to an angiotensin-converting enzyme-inhibitor or angiotensin-receptor blocker in subjects with type 2 diabetes mellitus and coronary artery disease.

Clinical trial registration

URL: http://www.clinicaltrials.gov. Unique identifier: NCT01624727.

Resumen vía Europe PMC. Los derechos de autor siguen siendo de los autores o la editorial (CC BY-NC-ND).

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