| Literature DB >> 25970146 |
Anne Whittaker1, Francesco Sofi2,3,4, Maria Luisa Eliana Luisi5, Elena Rafanelli6, Claudia Fiorillo7, Matteo Becatti8, Rosanna Abbate9, Alessandro Casini10, Gian Franco Gensini11, Stefano Benedettelli12.
Abstract
Khorasan wheat is an ancient grain with previously reported health benefits in clinically healthy subjects. The aim of this study was to examine whether a replacement diet, thereby substituting all other cereal grains, with products made with organic khorasan wheat could provide additive protective effects in reducing lipid, oxidative and inflammatory risk factors, in patients with Acute Coronary Syndromes (ACS) in comparison to a similar replacement diet using products made from organic modern wheat. A randomized double-blinded crossover trial with two intervention phases was conducted on 22 ACS patients (9 F; 13 M). The patients were assigned to consume products (bread, pasta, biscuits and crackers) made either from organic semi-whole khorasan wheat or organic semi-whole control wheat for eight weeks in a random order. On average, patients ingested 62.0 g dry weight (DW) day-1 khorasan or control semolina; and 140.5 g DW day-1 khorasan or control flour, respectively. An eight-week washout period was implemented between the respective interventions. Blood analyses were performed both at the beginning and end of each intervention phase; thereby permitting a comparison of both the khorasan and control intervention phases, respectively, on circulatory risk factors for the same patient. Consumption of products made with khorasan wheat resulted in a significant amelioration in total cholesterol (-6.8%), low-density lipoprotein cholesterol (LDL-C) (-8.1%) glucose (-8%) and insulin (-24.6%) from baseline levels, independently of age, sex, traditional risk factors, medication and diet quality. Moreover, there was a significant reduction in reactive oxygen species (ROS), lipoperoxidation of circulating monocytes and lymphocytes, as well as in the levels of Tumor Necrosis Factor-alpha. No significant differences from baseline in the same patients were observed after the conventional control wheat intervention phase. The present results suggest that a replacement diet with cereal products made from organic khorasan wheat provides additional protection in patients with ACS. Circulating cardiovascular risk factors, including lipid parameters, and markers of both oxidative stress and inflammatory status, were reduced, irrespective of the number and combination of medicinal therapies with proven efficacy in secondary prevention.Entities:
Keywords: acute coronary syndrome; conventional wheat; diet; khorasan wheat; secondary prevention
Mesh:
Substances:
Year: 2015 PMID: 25970146 PMCID: PMC4446758 DOI: 10.3390/nu7053401
Source DB: PubMed Journal: Nutrients ISSN: 2072-6643 Impact factor: 5.717
Composition of khorasan wheat and control wheat.
| Variable | Khorasan Wheat (Semolina) | Control wheat (Semolina) | Khorasan Wheat (Flour) | Control Wheat (Flour) | ||
|---|---|---|---|---|---|---|
| 14.6 ± 0.07 | 13.3 ± 0.11 | 0.3 | 14.7 ± 0.06 | 13.9 ± 0.09 | 0.3 | |
| 6.06 ± 0.41 | 5.80 ± 0.54 | 0.8 | 6.04 ± 0.33 | 5.08 ± 0.16 | 0.03 | |
| 1.23 ± 0.04 | 1.29 ± 0.06 | 0.4 | 1.05 ± 0.04 | 0.98 ± 0.03 | 0.03 | |
| 0.23 ± 0.02 | 0.24 ± 0.03 | 0.5 | 0.20 ± 0.03 | 0.11 ± 0.07 | 0.001 | |
| 18.1 ± 1.61 | 15.3 ± 0.28 | 0.03 | 15.3 ± 0.21 | 5.81 ± 0.06 | 0.02 | |
| 1.18 ± 0.08 | 0.81 ± 0.20 | 0.3 | 1.16 ± 0.09 | 0.48 ± 0.20 | 0.04 | |
| 22.9 ± 1.27 | 23.6 ± 0.38 | 0.2 | 21.4 ± 1.41 | 13.6 ± 3.15 | 0.08 | |
| 1819 ± 25.5 | 1989 ± 346.5 | 0.5 | 1732.5 ± 81.3 | 1221.5 ± 474.5 | 0.7 | |
| 1044.2 ± 70.4 | 915.4 ± 89.4 | 0.3 | 978.1 ± 0.35 | 672.2 ± 234.9 | 0.2 | |
| 2114.5 ± 71.4 | 1925.5 ± 303.3 | 0.1 | 2045 ± 91.9 | 1422.5 ± 391 | 0.3 | |
| 1.82 ± 0.15 | 1.08 ± 0.39 | 0.02 | 1.19 ± 0.14 | 0.50 ± 0.11 | 0.04 | |
| 21.1 ± 0.22 | 21.5 ± 0.92 | 0.1 | 19.4 ± 1.11 | 13.6 ± 5.04 | 0.6 |
Data are reported as mean ± SD; One-way ANOVA test.
Modifications in biochemical parameters a.
| Variable | Khorasan Pre | Khorasan Post | Control Pre | Control Post | Change, Khorasan | Change, Control | |
|---|---|---|---|---|---|---|---|
| 5.55 (5.14–5.96) | 5.11 (4.85–5.37) * | 5.29 (4.95–5.65) | 5.38 (5.08–5.69) | −0.44 (−0.76; −0.13) | 0.09 (−0.1; 0.27) | 0.03 | |
| 101.1 (70.2–132) | 76.2 (53.2–99.1) * | 94.9 (70.2–119.7) | 90.9 (64.9–117.1) | −24.9 (−41.6; −8.3) | −4.0 (−18.3; 10.3) | 0.006 | |
| 4.43 (3.96–4.90) | 4.13 (3.71–4.55) * | 4.36 (3.89–4.82) | 4.49 (4.03–4.94) | −0.30 (−0.45; −0.15) | 0.13 (−0.07; 0.34) | 0.001 | |
| 2.29 (1.96–2.64) | 2.11 (1.81–2.41) * | 2.32 (1.97–2.67) | 2.36 (2.02–2.70) | −0.18 (−0.28; −0.09) | 0.04 (−0.09; −0.17) | 0.001 | |
| 1.42 (1.24–1.61) | 1.39 (1.23–1.54) | 1.45 (1.26–1.64) | 1.41 (1.24–1.58) | −0.03 (−0.12; 0.05) | −0.04 (−0.13; 0.06) | 0.4 | |
| 1.39 (1.17–1.61) | 1.33 (1.10–1.55) | 1.29 (1.05–1.52) | 1.37 (1.16–1.57) | −0.06 (−0.14; 0.01) | 0.08 (−0.06; 0.23) | 0.2 | |
| 140.3 (139.4–141.1) | 139.9 (139–140.8) | 139.8 (138.9–140.6) | 139.9 (139.1–140.7) | −0.4 (−1.1; 0.4) | 0.1 (−0.7; 0.9) | 0.8 | |
| 4.34 (4.17–4.51) | 4.44 (4.26–4.62) | 4.31 (4.13–4.48) | 4.26 (4.09–4.43) | 0.10 (−0.08; 0.3) | −0.05 (−0.2; 0.08) | 0.5 | |
| 0.87 (0.84–0.89) | 0.89 (0.87–0.91) * | 0.90 (0.86–0.94) | 0.80 (0.68–0.92) | 0.02 (0.002; 0.5) | −0.10 (−0.22; 0.02) | 0.04 | |
| 1.09 (1.03–1.15) | 1.12 (1.04–1.19) | 1.12 (1.06–1.18) | 1.12 (1.05–1.18) | 0.03 (−0.07; 0.14) | 0 (−0.04; 0.04) | 0.9 | |
| 15 (12.6–17.4) | 16.1 (13.4–18.8) | 15.6 (12.6–18.7) | 17.1 (13.6–20.5) | 1.1 (−1.1; 3.3) | 1.5 (−1.8; 4.7) | 0.3 |
Data are reported as geometric mean and (range). General linear model adjusted for age, gender, number of medications, adherence score to MDLDL: Low-Density Lipoprotein; HDL: High-Density Lipoprotein. * p < 0.05 for comparison between pre- and post-intervention values (paired t-test). a Comparison between absolute changes induced by the two interventions (General linear model for repeated measurements).
Modifications in oxidative stress—related parameters a.
| Variable | Khorasan Pre | Khorasan Post | Control Pre | Control Post | Change, Khorasan | Change, Control | |
|---|---|---|---|---|---|---|---|
| 1432 (1302.2–1561.9) | 1274 (1149.3–1398.8) * | 1355.2 (1200.5–1509.9) | 1395 (1241.2–1548.8) | −158 (−306.1; −9.8) | 39.8 (−94.5; 174.1) | 0.003 | |
| 2671.9 (2154.9–2925.6) | 2317.6 (2113.7–2521.5) * | 2642.9 (2154.9–2770.9) | 2595.9 (2265.6–2926.3) | −354.2 (−568.9; −139.6) | 133.1 (−3.9; −270.1) | 0.002 | |
| 3177.1 (2851.9–3502.3) | 3228.7 (2808.8–3648.7) | 3760.7 (3159.5–4361.9) | 3386.1 (2956.8–3815.4) | 51.6 (-292.7; 395.9) | −374.6 (−922.8; 180.6) | 0.2 | |
| 8.06 (7.66–8.46) | 8.37 (7.85–8.89) | 7.88 (7.44–8.32) | 7.84 (7.39–8.28) | 0.31 (−0.09; 0.7) | −0.04 (−0.6; 0.5) | 0.9 | |
| 6.94 (5.04–8.83) | 6.89 (5.15–8.63) | 7.49 (5.37–9.61) | 6.44 (4.4–8.48) | −0.05 (−0.8; 0.7) | −1.05 (−2.1; 0.02) | 0.06 | |
| L-lipoperox, RFU | 2105.6 (1868.9–2342.2) | 1779.3 (1544.1–2014.5) * | 2215 (1876.7–2553.4) | 1908.2 (1690.2–2126.2) | −326.3 (-601.4; −51.1) | −306.9 (−677.4; 63.7) | 0.004 |
| M-lipoperox, RFU | 4869.7 (4273.3–5466.1) | 4244.1 (3830.4–4657.8) * | 4926.9 (4114.2–5739.7) | 4977.8 (4386.6–5569.1) | −625.5 (−1097.5; −153.6) | 50.9 (−796; 897.7) | 0.001 |
| G-lipoperox, RFU | 6892.5 (6240.9–7544) | 7049.3 (6232.8–7864.8) | 8025.3 (6733.2–9317.3) | 7518.5 (6635.3–8401.6) | 156.8 (−589.4; 903.1) | −506.8 (−1705.8; 692.1) | 0.4 |
L = lymphocytes; M = monocytes; G = granulocytes; ROS = Reactive Oxygen Species; TAC = Total Antioxidant Capacity; MDA = MalonDiAldehyde; Lipoperox = lipoperoxidation; RFU = Relative Fluorescence Unit. Data are reported as geometric mean and (range). General linear model adjusted for age, gender, number of medications, adherence score to MDLDL: Low-Density Lipoprotein; HDL: High-Density Lipoprotein. * p < 0.05 for comparison between pre- and post-intervention values (paired t-test). a Comparison between absolute changes induced by the two interventions (General linear model for repeated measurements).
Modifications in the inflammatory profile a.
| Variable | Khorasan Pre | Khorasan Post | Control Pre | Control Post | Change, Khorasan | Change, Control | |
|---|---|---|---|---|---|---|---|
| 38.2 (11.2–65.5) | 30.4 (15.1–45.7) | 40.8 (26.6–55) | 36.8 (24.8–48.8) | −7.8 (−36.5; 20.9) | −4 (−15.7; 7.6) | 0.5 | |
| 0.48 (0.27–0.68) | 0.44 (0.16–0.72) | 0.48 (0.21–0.76) | 0.51 (0.26–0.76) | −0.04 (−0.3; 0.2) | 0.03 (−0.4; 0.5) | 0.1 | |
| 2.26 (1.50–3.03) | 1.53 (1.16–1.90) | 3.16 (1.51–4.81) | 3.30 (1.24–6.37) | −0.73 (−1.6; 0.1) | 0.14 (−3.3; 3.6) | 0.9 | |
| 10.9 (6.2–15.5) | 5.6 (3.2–8) | 8.1 (6.2–10) | 12.7 (3.3–22.1) | −5.3 (−11.1; 0.5) | 4.6 (−5; 14.3) | 0.4 | |
| 11.6 (4.9–18.3) | 9.6 (5.5–13.7) | 10 (7–12.9) | 13.6 (2.9–29.9) | −2 (−7.8; 3.9) | 3.6 (−3.2; 20.4) | 0.3 | |
| 30.8 (14.3–47.3) | 24.2 (15.6–32.8) | 22.2 (13.3–31.2) | 23.8 (11.9–35.6) | −6.6 (−18.8; 5.6) | 1.6 (−9.4; 12.5) | 0.6 | |
| 4.2 (1.3–7) | 8.4 (4.9–11.8) | 8.6 (2.6–14.6) | 6.6 (3.2–10) | 4.2 (−1.7; 10.1) | −2 (−8.3; 4.3) | 0.4 | |
| 21.6 (12.8–30.5) | 13.8 (9.2–18.5) | 23.2 (15.9–30.7) | 19.2 (10.9–27.5) | −7.8 (−16; 0.4) | −4 (−15.8; 7.6) | 0.5 | |
| 43.8 (31.6–56.1) | 72.2 (50.6–93.7) | 61.9 (39.6–84.4) | 47.9 (30.1–65.8) | −8.1 (−30.7; 14.5) | −14 (−33.8; 5.7) | 0.3 | |
| 80.3 (59–101.6) | 72.2 (50.6–93.7) | 88.7 (61.1–108.4) | 73 (54.3–91.6) | −8.1 (−30.7; 14.5) | −15.8 (−33.9; 2.4) | 0.7 | |
| 8.3 (3.9–12.6) | 3.9 (1.4–6.4) * | 6.5 (2.9–9.9) | 4.6 (0.9–8.2) | −4.4 (-8.7; −0.007) | −1.9 (−5.5; 1.7) | 0.04 | |
| 170.4 (90–250.9) | 124.1 (64.7–183.6) | 137.6 (74.9–200.2) | 93.2 (44.9–142.4) | −46.3 (−97; 4.4) | −44.4 (−97.1; 8.2) | 0.9 |
INF-gamma = Interferon-gamma; MCP-1 = Monocyte Chemotactic Protein-1; MIP-1beta = Macrophage Inflammatory Protein-1 beta; TNF-alpha = Tumour Necrosis Factor-alpha; VEGF = Vascular Endothelial Growth Factor. Data are reported as geometric mean and (range). General linear model adjusted for age, gender, number of medications, adherence score to MD. * p < 0.05 for comparison between pre- and post-intervention values (paired t-test). a Comparison between absolute changes induced by the two interventions (General linear model for repeated measurements).