In their study, Choi et al. 5 noted that cilostazol, a PDE3 inhibitor, could experimentally promote hair growth by stimulating human dermal papilla cell (hDPC) proliferation, enhancing hair shaft elongation and prolongation of anagen induction in C57BL/6 mice. Later, Choi et al. 6 measured the expression of PDE5A and found that PDE5A mRNA and protein were highly expressed in hDPCs and human hair follicles (hHFs). Sildenafil also increased the mRNA expression of vascular endothelial growth factor (VEGF) and platelet-derived growth factor (PDGF) in hDPCs, which stimulate secretion of these factors, and can promote proliferation of hDPCs. Further, sildenafil may affect perifollicular angiogenesis around hair follicles and prolong the anagen hair cycle. Apremilast, a phosphodiesterase 4 inhibitor, showed a significant improvement of extensive, refractory alopecia areata. Furthermore, apremilast significantly reduces TGF-b1-induced fibroblast migration and inhibits dermal fibroblast differentiation into myofibroblasts that is mediated by TGF-b1 in psoriatic patients. 7,8 TGF-b1 signalling is a critical driver of collagen accumulation and fibrotic diseases but also a vital suppressor of inflammation and epithelial cell proliferation. We agree with the hypothesis delivered by Chen et al., 1 and we thought that attenuating/ameliorating drugs of TGF-b1 signalling, and its pro-fibrotic activity, such as PDEI may represent a future hope for hair disorders. These drugs/agents can be useful alone or in combination as a therapeutic for disorders with perifollicular fibrosis, such as AGA. Chen et al.'s study, 1 though a preliminary, may pave the way to better understanding of AGA. Further research into drug-delivery, ideal topical concentration or oral dose and frequency, and side effects of these drugs is warranted. As per our speculation, PDEI drugs may be a promising therapy for AGA.