TY - JOUR
T1 - Reply-letter to the editor-effects of omega-3 polyunsaturated fatty acid intake in patients with chronic kidney disease
T2 - Systematic review and meta-analysis of randomized controlled trials
AU - Saglimbene, Valeria M.
AU - Wong, Germaine
AU - Teixeira-Pinto, Armando
AU - Craig, Jonathan C.
AU - Strippoli, Giovanni F.M.
PY - 2019/10
Y1 - 2019/10
N2 - We thank Kumar A. and Shariff M et al. for conducting a trial sequential analysis (TSA) on our meta-analysis of omega 3 fatty acid supplementation in chronic kidney disease. The authors estimated the required information size and trial sequential boundary to determine if the observed beneficial effect of omega 3 supplementation on cardiovascular mortality is conclusive or whether further evidence is needed. They found that an information size of 1314 is needed to detect a risk reduction of 56% in cardiovascular mortality with omega 3 supplementation. They assumed a power of 80%, an alpha of 5%, cardiovascular mortality rate of 5.26% in the control arm, and a diversity (D2) of 0%. While the required information size was not achieved (1314 versus a pooled information size of 1104 in our meta-analysis), the authors reported the z curve crossed the estimated trial sequential boundary after study 8. Therefore, they concluded that there is sufficient evidence to confirm the benefits of omega-3 supplementation on cardiovascular mortality and no further trials are needed. Of note, the estimates of effects and study heterogeneity were sourced from our meta-analyses.
AB - We thank Kumar A. and Shariff M et al. for conducting a trial sequential analysis (TSA) on our meta-analysis of omega 3 fatty acid supplementation in chronic kidney disease. The authors estimated the required information size and trial sequential boundary to determine if the observed beneficial effect of omega 3 supplementation on cardiovascular mortality is conclusive or whether further evidence is needed. They found that an information size of 1314 is needed to detect a risk reduction of 56% in cardiovascular mortality with omega 3 supplementation. They assumed a power of 80%, an alpha of 5%, cardiovascular mortality rate of 5.26% in the control arm, and a diversity (D2) of 0%. While the required information size was not achieved (1314 versus a pooled information size of 1104 in our meta-analysis), the authors reported the z curve crossed the estimated trial sequential boundary after study 8. Therefore, they concluded that there is sufficient evidence to confirm the benefits of omega-3 supplementation on cardiovascular mortality and no further trials are needed. Of note, the estimates of effects and study heterogeneity were sourced from our meta-analyses.
KW - chronic kidney disease (CKD)
KW - omega-3
KW - systematic review
UR - http://www.scopus.com/inward/record.url?scp=85072580440&partnerID=8YFLogxK
U2 - 10.1016/j.clnu.2019.07.005
DO - 10.1016/j.clnu.2019.07.005
M3 - Comment/debate
C2 - 31387761
AN - SCOPUS:85072580440
VL - 38
SP - 2462
JO - CLINICAL NUTRITION
JF - CLINICAL NUTRITION
SN - 0261-5614
IS - 5
ER -