Department of Dermatology, College of Medicine, Dongguk University Ilsan Hospital, 814 Siksa-dong, Ilsandong-gu, Goyang-si 410-773, Gyeonggi-do, Korea.
Int J Mol Sci. 2021 Apr 2;22(7):3727. doi: 10.3390/ijms22073727.
Skin disorders showing abnormal pigmentation are often difficult to manage because of their uncertain etiology or pathogenesis. Abnormal pigmentation is a common symptom accompanying aging skin. The association between skin aging and skin pigmentation abnormalities can be attributed to certain inherited disorders characterized by premature aging and abnormal pigmentation in the skin and some therapeutic modalities effective for both. Several molecular mechanisms, including oxidative stress, mitochondrial DNA mutations, DNA damage, telomere shortening, hormonal changes, and autophagy impairment, have been identified as involved in skin aging. Although each of these skin aging-related mechanisms are interconnected, this review examined the role of each mechanism in skin hyperpigmentation or hypopigmentation to propose the possible association between skin aging and pigmentation abnormalities.
皮肤色素异常疾病的病因或发病机制常不明确,因此往往难以治疗。色素异常是衰老皮肤的常见伴随症状。皮肤老化与皮肤色素异常的关联可能与某些以皮肤过早老化和色素异常为特征的遗传性疾病以及某些对两者均有疗效的治疗方法有关。几种分子机制,包括氧化应激、线粒体 DNA 突变、DNA 损伤、端粒缩短、激素变化和自噬障碍,已被确定与皮肤老化有关。虽然这些与皮肤老化相关的机制相互关联,但本综述检查了每种机制在皮肤色素过度沉着或色素减退中的作用,以提出皮肤老化与色素异常之间可能存在的关联。