Supplementation with cod protein hydrolysate in older adults: a dose range cross-over study

Caroline Jensen, Hanna F Dale, Trygve Hausken, Einar Lied, Jan G Hatlebakk, Ingeborg Brønstad, Gülen A Lied, Dag Arne L Hoff, Caroline Jensen, Hanna F Dale, Trygve Hausken, Einar Lied, Jan G Hatlebakk, Ingeborg Brønstad, Gülen A Lied, Dag Arne L Hoff

Abstract

A large proportion of older adults are affected by impaired glucose metabolism. Previous studies with fish protein have reported improved glucose regulation in healthy adults, but the evidence in older adults is limited. Therefore, we wanted to assess the effect of increasing doses of a cod protein hydrolysate (CPH) on postprandial glucose metabolism in older adults. The study was a double-blind cross-over trial. Participants received four different doses (10, 20, 30 or 40 mg/kg body weight (BW)) of CPH daily for 1 week with 1-week washout periods in between. The primary outcome was postprandial response in glucose metabolism, measured by samples of serum glucose and insulin in 20 min intervals for 120 min. The secondary outcome was postprandial response in plasma glucagon-like peptide 1 (GLP-1). Thirty-one subjects aged 60-78 years were included in the study. In a mixed-model statistical analysis, no differences in estimated maximum value of glucose, insulin or GLP-1 were observed when comparing the lowest dose of CPH (10 mg/kg BW) with the higher doses (20, 30 or 40 mg/kg BW). The estimated maximum value of glucose was on average 0·28 mmol/l lower when the participants were given 40 mg/kg BW CPH compared with 10 mg/kg BW (P = 0·13). The estimated maximum value of insulin was on average 5·14 mIU/l lower with 40 mg/kg BW of CPH compared with 10 mg/kg BW (P = 0·20). Our findings suggest that serum glucose and insulin levels tend to decrease with increasing amounts of CPH. Due to preliminary findings, the results require further investigation.

Keywords: BW, body weight; CPH, cod protein hydrolysate; Cod protein; Fish protein; GLP-1, glucagon-like peptide 1; Glucose homeostasis; Marine peptides; Marine protein hydrolysate.

© The Author(s) 2019.

Figures

Fig. 1.
Fig. 1.
Flowchart depicting the inclusion and randomisation process. BW, body weight.
Fig. 2.
Fig. 2.
Metabolic responses for serum glucose (a), serum insulin (b) and plasma glucagon-like peptide 1 (GLP-1) (c) concentrations after intake of a standardised breakfast meal and the last dosage of the cod protein hydrolysate (CPH). Dose levels were 10, 20, 30 and 40 mg/kg body weight (BW). Results for serum glucose and insulin are presented for all thirty-one subjects, whereas for GLP-1 the results are presented for twenty-seven subjects (four participants were excluded from the statistical analysis due to analytical errors). Values are means. Time point 0 min is the first postprandial blood sample, taken 25 min after the drink was served and 15 min after the breakfast meal started. BL, baseline.
Fig. 3.
Fig. 3.
Bar chart depicting the total AUC for serum glucose (a), serum insulin (b) and plasma glucagon-like peptide 1 (GLP-1) (c) after intake of a standardised breakfast meal and the last dosage of cod protein hydrolysate (CPH) in the dose level. Dose levels were 10, 20, 30 and 40 mg/kg body weight (BW). Values are means, with standard errors represented by vertical bars. No statistically significant differences in AUC between the four different doses were observed for any of the outcome measures when comparing the lowest dose of 10 mg/kg BW of CPH with the higher doses of 20, 30 or 40 mg/kg BW.

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Source: PubMed

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