LRP1B mutations in GC may be associated with the progression of GC.[31] Consistent with the above research, in the premalignant and early-stage GCA, and stage IIB to IV GCA, the mutation rates of TP53, ARID1A, and LRP1B are relatively high, and there is no significant difference between the early and late stages. This evidence concerns the gene ARID1A and temporal arteritis.