Raman spectral variation for human fingernails of postmenopausal women is dependent on fracture risk and osteoporosis status

被引:19
作者
Beattie, J. R. [1 ]
Caraher, M. C. [2 ]
Cummins, N. M. [3 ]
O'Driscoll, O. M. [4 ]
Eastell, R. [5 ]
Ralston, S. H. [6 ]
Towler, M. R. [7 ,8 ]
机构
[1] Exploristics Ltd, Floor 4,24 Linenhall St, Belfast BT2 8BG, Antrim, North Ireland
[2] ICON Plc, Dublin, Ireland
[3] Univ Limerick, Grad Entry Med Sch, Ctr Intervent Infect Inflammat & Immun, Limerick, Ireland
[4] Cork Inst Technol, Med Engn Design & Innovat Ctr, Cork, Ireland
[5] Northern Gen Hosp, Metab Bone Ctr, Acad Unit Bone Metab, Sheffield, S Yorkshire, England
[6] Western Gen Hosp, Sch Mol & Clin Med, Edinburgh, Midlothian, Scotland
[7] Univ Malaya, Dept Biomed Engn, Fac Engn, Kuala Lumpur, Malaysia
[8] Ryerson Univ, Dept Mech & Ind Engn, Toronto, ON, Canada
关键词
keratin; bone health; fracture risk; osteoporosis; protein; HIP FRACTURE; ELDERLY-WOMEN; HUMAN NAIL; SPECTROSCOPY; COLLAGEN; MODEL; TOOL;
D O I
10.1002/jrs.5123
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
Patients diagnosed with osteoporosis have reported loss of fingernail resilience as the disease progresses. Keratin is the predominant protein in human nail tissue, and its structure has been postulated to be different in fingernails clipped from subjects who have sustained fragility fractures and those who have not, which may offer a window into the donor's bone health. This study was designed to qualify these differences, which may lead to the development of a novel screening tool for fracture risk. Raman spectroscopy was used to measure the fingernails of 633 postmenopausal women who presented at six fracture clinics located across the UK and Ireland. The Raman signals from donor's fingernails were compared between (1) fracture and nonfracture and (2) osteoporotic versus non-osteoporotic donors The data presented show differences in the protein changes observed for pervasive osteoporosis compared to a general increased risk of fragility fracture. For fracture risk, compositional changes falling into broad classes of amino acid residue (aliphatic, aromatic, acidic, amide and sulphurous) were observed, while a difference in disulphide bonding levels was reaffirmed. For pervasive osteoporosis, the disulphide mode suggested increasing disorder in disulphide bonding orientation. Fractures were associated with a transition from alpha helical secondary structure to random, while the pervasive osteoporosis cases were associated with a transition to beta sheet structure. General fracture risk is associated with a change in the structure and composition of the keratin protein. Osteoporosis is associated with different protein structural changes and an increase in free acid groups. Copyright (c) 2017 John Wiley & Sons, Ltd.
引用
收藏
页码:813 / 821
页数:9
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