TY - JOUR
T1 - Dietary inflammatory index and risk of multiple sclerosis
T2 - Findings from a large population-based incident case–control study
AU - Abdollahpour, Ibrahim
AU - Jakimovski, Dejan
AU - Shivappa, Nitin
AU - Hébert, James R.
AU - Vahid, Farhad
AU - Nedjat, Saharnaz
AU - Mansournia, Mohammad Ali
AU - Weinstock-Guttman, Bianca
N1 - Publisher Copyright:
© 2020 Elsevier Ltd and European Society for Clinical Nutrition and Metabolism
PY - 2020/11
Y1 - 2020/11
N2 - Background & aims: For many decades diet, mainly its “pro-inflammatory” quality has been pondered as a possible risk factor for developing MS. However, the complexity of different dietary composition analysis provided controversial results. Recently a dietary inflammatory index (DII), a population-based score, was developed to objectify the inflammatory characteristics of a specific dietary intake. Methods: We investigated the potential association between DII (expressed as energy adjusted-DII (E-DII) and non-energy adjusted DII (DII)) assessed from a validated FFQ based on the participants' diet habits during adolescence and the risk for developing MS in a population-based incident case–control study. Multiple logistic regression was used to estimate the adjusted. Results: We recruited 547 incident MS cases and 1057 general population controls from Tehran, Iran (August 2013–February 2015). A statistically significant higher risk of MS was found in analyses using E-DII scores as a continuous variable with an adjusted odds ratio (AOR) of 1.53 (95% confidence interval (CI): 1.42–1.65, P = 0.001), and as a categorical variable (4th quartile OR 7.01, 95% CI: 4.87–10.1, vs the first quartile), test for trend; OR 1.86 (95% CI: 1.67–2.07), P for trend <0.001. A similar pattern was demonstrated for DII score and risk for MS. Conclusions: We identified a pro-inflammatory diet characterized by higher E-DII and DII scores during adolescence as a strong risk factor for MS onset. Given the worldwide role of diet in general population health, improving nutritional pattern through educational programs is likely to reduce MS risk.
AB - Background & aims: For many decades diet, mainly its “pro-inflammatory” quality has been pondered as a possible risk factor for developing MS. However, the complexity of different dietary composition analysis provided controversial results. Recently a dietary inflammatory index (DII), a population-based score, was developed to objectify the inflammatory characteristics of a specific dietary intake. Methods: We investigated the potential association between DII (expressed as energy adjusted-DII (E-DII) and non-energy adjusted DII (DII)) assessed from a validated FFQ based on the participants' diet habits during adolescence and the risk for developing MS in a population-based incident case–control study. Multiple logistic regression was used to estimate the adjusted. Results: We recruited 547 incident MS cases and 1057 general population controls from Tehran, Iran (August 2013–February 2015). A statistically significant higher risk of MS was found in analyses using E-DII scores as a continuous variable with an adjusted odds ratio (AOR) of 1.53 (95% confidence interval (CI): 1.42–1.65, P = 0.001), and as a categorical variable (4th quartile OR 7.01, 95% CI: 4.87–10.1, vs the first quartile), test for trend; OR 1.86 (95% CI: 1.67–2.07), P for trend <0.001. A similar pattern was demonstrated for DII score and risk for MS. Conclusions: We identified a pro-inflammatory diet characterized by higher E-DII and DII scores during adolescence as a strong risk factor for MS onset. Given the worldwide role of diet in general population health, improving nutritional pattern through educational programs is likely to reduce MS risk.
KW - Dietary inflammatory index (DII)
KW - Incident case–control study
KW - Iran
KW - Multiple sclerosis
KW - Nutrition
UR - http://www.scopus.com/inward/record.url?scp=85081662946&partnerID=8YFLogxK
U2 - 10.1016/j.clnu.2020.02.033
DO - 10.1016/j.clnu.2020.02.033
M3 - Article
C2 - 32197810
AN - SCOPUS:85081662946
SN - 0261-5614
VL - 39
SP - 3402
EP - 3407
JO - Clinical Nutrition
JF - Clinical Nutrition
IS - 11
ER -