Skin pigmentation is negatively associated with circulating vitamin D concentration and cutaneous microvascular endothelial function

• Published in: American journal of physiology. Heart and circulatory physiology Vol. 323; no. 3; pp. 490 - 498
• Main Authors: Wolf, S Tony, Dillon, Gabrielle A, Alexander, Lacy M, Jablonski, Nina G, Kenney, W Larry
• Format: Journal Article
• Language: English
• Published: United States American Physiological Society 01.09.2022
• Series: Integrative Cardiovascular Physiology and Pathophysiology
• Subjects: 25-Hydroxyvitamin D; Adults; Arginine; Bioavailability; Blood flow; Calciferol; Cytokines; Doppler effect; Enzyme-linked immunosorbent assay; Female; Heating; Humans; Inflammation; Interleukin 10; Interleukin 6; Male; Microdialysis; Microvasculature; Microvessels; NG-Nitroarginine Methyl Ester; Nitric Oxide; Nitric-oxide synthase; Oxidative stress; Pigmentation; Regional Blood Flow; Skin; Skin - blood supply; Skin Pigmentation; Sodium nitroprusside; Spectrophotometry; Tumor necrosis factor-α; Vasodilation; Vitamin D; Vitamin D Deficiency - diagnosis; Vitamin deficiency; Young Adult; Young adults; skin blood flow; nitric oxide; race; inflammation; melanin
• ISSN: 0363-6135; 1522-1539; 1522-1539
• DOI: 10.1152/ajpheart.00309.2022

Darkly pigmented individuals are at the greatest risk of hypovitaminosis D, which may result in microvascular endothelial dysfunction via reduced nitric oxide (NO) bioavailability and/or increased oxidative stress and inflammation. We investigated the associations among skin pigmentation (M-index; skin reflectance spectrophotometry), serum vitamin D concentration [25(OH)D], circulating inflammatory cytokine (TNF-α, IL-6, and IL-10) concentrations, and the NO contribution to local heating-induced cutaneous vasodilation (%NO-mediated vasodilation) in a diversely pigmented cohort of young adults. An intradermal microdialysis fiber was placed in the forearms of 33 healthy adults (14 men/19 women; 18-27 yr; M-index, 30-81 AU) for local delivery of pharmacological agents. Lactated Ringer's solution was perfused through the fiber during local heating-induced (39°C) cutaneous vasodilation. After attaining stable elevated blood flow, 15 mM -nitro-l-arginine methyl ester (l-NAME; NO synthase inhibiter) was infused to quantify %NO-mediated vasodilation. Red cell flux was measured (laser-Doppler flowmetry; LDF) and cutaneous vascular conductance (CVC = LDF/MAP) was normalized to maximal (%CVC ; 28 mM sodium nitroprusside + 43°C). Serum [25(OH)D] and circulating cytokines were analyzed by ELISA and multiplex assay, respectively. M-index was negatively associated with [25(OH)D] ( = -0.57, < 0.0001) and %NO-mediated vasodilation ( = -0.42, = 0.02). Serum[25(OH)D] was positively related to %NO ( = 0.41, = 0.02). Controlling for [25(OH)D] weakened the association between M-index and %NO-mediated dilation ( = 0.16, = -0.26). There was a negative curvilinear relation between [25(OH)D] and circulating IL-6 ( = -0.56, < 0.001), but not TNF-α or IL-10 ( ≥ 0.14). IL-6 was not associated with %NO-mediated vasodilation ( = 0.44). These data suggest that vitamin D insufficiency/deficiency may contribute to reduced microvascular endothelial function in healthy, darkly pigmented young adults. Endothelial dysfunction, an antecedent to hypertension and overt CVD, is commonly observed in otherwise healthy Black adults, although the underlying causes remain unclear. We show that reduced vitamin D availability with increasing degrees of skin pigmentation is associated with reduced microvascular endothelial function, independent of race or ethnicity, in healthy young adults. Greater prevalence of vitamin D deficiency in more darkly pigmented individuals may predispose them to increased risk of endothelial dysfunction.