“…MDD confers a 60% increased T2D risk (Mezuk, Eaton, Albrecht, & Golden, ), independently from antidepressant therapy (Pan et al, ). SCZ also increases T2D risk, unrelated to antipsychotic therapy, and SCZ patients have higher rates of prediabetes, T2D, MetS, and obesity than control subjects (Q. Li et al, ; Subashini, Deepa, Padmavati, Thara, & Mohan, ) and share common risk variants with MetS traits (Andreassen et al, ). Several studies have demonstrated that drug‐naive SCZ patients have impaired fasting glucose (IFG), impaired insulin action, and increased T2D risk (Dasgupta, Singh, Rout, Saha, & Mandal, ; Fernandez‐Egea et al, ; Ryan, Collins, & Thakore, ; van Nimwegen et al, ); and SCZ/nonaffective psychosis (NAP) are significantly associated with increased odds of parental T2D and first‐degree relatives' impaired‐glucose tolerance (IGT) (Fernandez‐Egea, Miller, Bernardo, Donner, & Kirkpatrick, ; Miller et al, ; Spelman, Walsh, Sharifi, Collins, & Thakore, ).…”