“…The incidence of IAS in Caucasians seems to be lower than in the Japanese population (Cappellani et al, 2020). However, the number of case reports regarding Caucasians has been increasing in recent years (Bresciani et al, 2011;Gullo et al, 2014;Michalopoulou Alevras et al, 2015;Lio et al, 2016;Ferreira et al, 2017;Bolayir et al, 2018;Cappellani et al, 2018;Veltroni et al, 2018;Alag € uney et al, 2019;Moffa et al, 2019;Cambria et al, 2020;Okuroglu et al, 2020;Yukina et al, 2020). It is, however, difficult to estimate the actual incidence or conclude on a true increase in the disease incidence among Caucasians, because of a possible underestimation of the occurrence of the syndrome linked to a possible unawareness of the disease and its subsequent underdiagnosis and underreporting (Cappellani et al, 2020).…”
Section: Epidemiology Of Insulin Autoimmune Syndromementioning
Following a request from the European Commission, the EFSA Panel on Nutrition, Novel Foods and Food Allergens (NDA) was asked to deliver an opinion on the relationship between alpha-lipoic acid (ALA) and the risk of insulin autoimmune syndrome (IAS). The Panel was also asked to advise on the dose below which ALA added to foods is not expected to cause IAS. A review of all possible adverse effects associated with consumption of ALA was not requested. This mandate refers to the procedure under Article 8(2) of Regulation (EC) No 1925/2006 on addition of vitamins, minerals and certain other substances to foods. No pre-established rule exists for the evaluation of the safety of foods when classical toxicity tests cannot be used, e.g. for autoimmune diseases. Published scientific evidence was retrieved through comprehensive literature searches, particularly 49 case reports in which IAS developed following ALA consumption. In all cases, IAS resolved after a few weeks to months when ALA was discontinued. No publication linking the intake of ALA naturally occurring in foods to IAS was identified. The Panel concludes that the consumption of ALA added to foods, including food supplements, is likely to increase the risk of developing IAS in individuals with certain genetic polymorphisms, who cannot be readily identified without genetic testing. The plausible mechanism of such an effect has not yet been fully elucidated. The incidence of IAS in Europe is low and likely lower than in Japan where it has been estimated to be 0.017 per 100,000 inhabitants in 2017-2018. Considering the limited data available, the risk associated with the development of IAS following ALA consumption cannot be quantified precisely. An ALA dose below which IAS is not expected to occur is likely to vary between individuals and cannot be determined from the available data.
“…The incidence of IAS in Caucasians seems to be lower than in the Japanese population (Cappellani et al, 2020). However, the number of case reports regarding Caucasians has been increasing in recent years (Bresciani et al, 2011;Gullo et al, 2014;Michalopoulou Alevras et al, 2015;Lio et al, 2016;Ferreira et al, 2017;Bolayir et al, 2018;Cappellani et al, 2018;Veltroni et al, 2018;Alag € uney et al, 2019;Moffa et al, 2019;Cambria et al, 2020;Okuroglu et al, 2020;Yukina et al, 2020). It is, however, difficult to estimate the actual incidence or conclude on a true increase in the disease incidence among Caucasians, because of a possible underestimation of the occurrence of the syndrome linked to a possible unawareness of the disease and its subsequent underdiagnosis and underreporting (Cappellani et al, 2020).…”
Section: Epidemiology Of Insulin Autoimmune Syndromementioning
Following a request from the European Commission, the EFSA Panel on Nutrition, Novel Foods and Food Allergens (NDA) was asked to deliver an opinion on the relationship between alpha-lipoic acid (ALA) and the risk of insulin autoimmune syndrome (IAS). The Panel was also asked to advise on the dose below which ALA added to foods is not expected to cause IAS. A review of all possible adverse effects associated with consumption of ALA was not requested. This mandate refers to the procedure under Article 8(2) of Regulation (EC) No 1925/2006 on addition of vitamins, minerals and certain other substances to foods. No pre-established rule exists for the evaluation of the safety of foods when classical toxicity tests cannot be used, e.g. for autoimmune diseases. Published scientific evidence was retrieved through comprehensive literature searches, particularly 49 case reports in which IAS developed following ALA consumption. In all cases, IAS resolved after a few weeks to months when ALA was discontinued. No publication linking the intake of ALA naturally occurring in foods to IAS was identified. The Panel concludes that the consumption of ALA added to foods, including food supplements, is likely to increase the risk of developing IAS in individuals with certain genetic polymorphisms, who cannot be readily identified without genetic testing. The plausible mechanism of such an effect has not yet been fully elucidated. The incidence of IAS in Europe is low and likely lower than in Japan where it has been estimated to be 0.017 per 100,000 inhabitants in 2017-2018. Considering the limited data available, the risk associated with the development of IAS following ALA consumption cannot be quantified precisely. An ALA dose below which IAS is not expected to occur is likely to vary between individuals and cannot be determined from the available data.
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