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肾性骨病患者中医证候特征与透析龄、原发病及其生存质量的相关性研究
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摘要
肾性骨病(Renal osteodystrophy, ROD)是慢性肾功能不全患者常见的并发症,几乎累及慢性肾脏病终末期的所有患者。ROD是由慢性肾功能衰竭导致钙磷代谢紊乱的一种骨骼形态学变化的代谢性骨病,可引起骨强度的改变、骨生长的异常,进而加重钙磷代谢的紊乱,引起皮肤瘙痒、贫血、神经系统及心血管系统损害等,严重影响了患者的存活率及生存质量。随着血液透析技术的发展,慢肾衰患者的存活率及生存时间得到了提高与延长,因而其生存质量受到了广泛的关注。随着慢性肾衰竭患者的增加,肾性骨病日益增多,近年来在西医常规治疗肾性骨病的基础上,联合中医药治疗在防治肾性骨病方面发挥了巨大的作用,优势逐渐显现。本课题采用横断面研究,观察了不同透析龄及原发病肾性骨病患者证候分布规律及不同证候、透析龄患者的生存质量,探索不同透析龄及原发病患者的中医证候分布特征、演变规律,及不同证候、透析龄患者的生存质量变化特点。
     1研究目的
     本研究通过对长期维持性血液透析的慢性肾衰肾性骨病患者进行横断面观察,统计观察其在不同透析龄及不同原发病的中医证候分布规律特点,及不同证候、透析龄患者的生存质量,为临床联合中医药治疗肾性骨病提供相对客观评价依据。
     2研究方法
     入选符合纳入标准的肾性骨病患者,共192例,对所有入组的患者进行症状学调查并记录,根据肾性骨病中医证候特点对所有入选病例进行辨证分型,分为阴阳两虚、痰瘀互阻(a),阳虚湿盛、痰浊内阻(b),阴虚内热、痰浊内阻(c)三组。①观察各组患者在不同透析龄(≤36月A、36-72月B、>72月C三组)及不同原发病(慢性肾小球肾炎Ⅰ、糖尿病Ⅱ、高血压Ⅲ、其他Ⅳ四组)出现频率及分布特征;②研究对比所纳入的192例肾性骨病患者中a、b、c三组不同证候患者的生存质量,及A、B、C三组不同透析龄患者的生存质量。
     3研究结果
     3.1不同透析龄ROD,患者的中医证候分布
     透析龄小于36个月及透析龄为36~72个月的ROD患者中阴阳两虚、阳虚、阴虚三组的分布无明显差异。而透析龄大于72个月的患者中阴阳两虚型所占比例最高(55.6%),阴虚及阳虚型分布相对较少,且两组间无明显差异。
     3.2不同原发病ROD患者的中医证候分布
     ①原发病为慢性肾小球肾炎的患者中阴阳两虚型所占比例最高,阴虚与阳虚型较少。②原发病为糖尿病的患者中阴虚型所占比例最高,阴阳两虚型次之,阳虚型最少。③原发病为高血压的患者中各型分布无显著差异。④原发病为其他的患者各证候分布为阴阳两虚最多,阳虚次之,阴虚型最少。
     3.3不同透析龄组的原发病分布情况
     随着透析龄的增长原发病为慢性肾小球肾炎的患者逐渐增多,糖尿病肾病的患者逐渐减少,而原发病为高血压的患者分布无明显规律。
     3.4ROD患者生存质量与中医证候的关系
     生理功能、躯体疼痛、总体健康方面:a组最差,b、c组间无明显差异;生理职能、精力评分、社会职能方面:a组最差,且较b、c组有非常显著性差异(P均<0.01),而b、c组间无明显差异;感情职能方面:a组与b、c组无明显差异,c组较b组理想;心理健康方面:c组最理想,b组次之,a组最差;生理健康总测量:a组最差,b、c较之理想;精神健康总测量:c组最理想,b组次之,a组最差;生存质量总分评价:a组最差,b、c较之理想。
     3.5ROD患者生存质量与透析龄的关系
     生理功能、生理职能、躯体疼痛、精力评分、社会职能方面C组患者最差,A组最理想;一般健康状况:A最优,C次之,B最差;感情职能:A最差,C次之,B最优;心理健康:C最优,B次之,A最差;生理健康总测量:A最优,B次之,C最差;精神健康总测量:B最优,A次之,C最差;生存质量总分:B最优,A次之,C最差。
     4结论
     4.1ROD患者的证候变化特点基本符合疾病发展规律的趋势,伴随透析龄及病程的渐长,阴阳两虚、痰瘀互阻证最为常见,与肾性骨病的本虚标实、虚实夹杂的病机特点一致。
     4.2原发病为慢性肾小球肾炎的ROD患者多见阴阳两虚证,原发病为糖尿病的患者多见阴虚型及阴阳两虚型,阳虚型较少,原发病为高血压的患者中证候分布无显著差异,其分布特点考虑与各原发病本证之病机特点相关,可以作为中医辨证施治的参考依据。
     4.3原发病为慢性肾小球肾炎的患者透析龄较长,生存时间相对较长,糖尿病肾病的患者透析龄较短,生存时间相对较短。
     4.4阴阳两虚组患者在涉及生理健康方面的生存质量评分最差;在涉及心理健康方面的生存质量评分,阴虚组最理想,阳虚组次之,阴阳两虚组最差,符合肾性骨病病机发展规律;但阴虚组较阳虚组心理健康理想,可能与阳虚型患者脾肾阳虚的病机特点有关,以上规律为中医早期介入对证治疗以改善患者生存质量提供了依据。
     4.5透析龄大于72个月的患者在涉及生理健康方面的生存质量评分最差,透析龄为36-72个月的患者次之,小于36个月的最理想;涉及精神健康方面的生存质量评分透析龄在36~72个月的患者最理想,小于36个月的次之,大于72个月的最差。
Renal osteodystrophy (ROD) is common in patients with chronic renal insufficiency complications, almost involving the end-stage of chronic kidney disease patients. ROD lead to morphological changes in metabolic bone of a skeleton of calcium and phosphorus metabolism disorders, chronic renal failure can cause changes in bone strength, bone growth abnormalities, thereby increasing the calcium and phosphorus metabolism disorders, itching of skin, anemia nervous system and cardiovascular system damage, a serious impact on patient survival and quality of life. With the development of hemodialysis, chronic renal failure patients, the survival rate and survival time to improve and extend, and thus their quality of life has received extensive attention. With the increase of patients with chronic renal failure, renal osteodystrophy increasing number in recent years on the basis of conventional Western medicine treatment of renal osteodystrophy, the joint treatment of Chinese medicine has played a huge role in the prevention and treatment of renal osteodystrophy, the advantage is gradually emerging. This topic is cross-sectional study to observe the quality of life of renal osteodystrophy in patients with different dialysis age and evidence of the primary disease syndrome distribution law, and different syndromes, dialysis age of patients, and explore each dialysis age and primary disease of TCM syndrome distribution features, evolution, and different syndromes, change characteristics of the patient's quality of life of dialysis age.
     1Research Purposes
     In this study, cross-sectional observation of the long-term hemodialysis patients with chronic renal failure, renal osteodystrophy, the statistics observed in different dialysis age and primary disease of TCM syndrome distribution laws of the characteristics of different syndromes, patients with dialysis agequality of life, relatively objective evaluation based on clinical joint Chinese medicine treatment of renal osteodystrophy.
     2Rresearch Methods
     Selected met the inclusion criteria in patients with renal osteodystrophy, a total of192cases, symptomatology survey and record all the enrolled patients, according to the renal osteodystrophy of TCM syndrome type designate the characteristics of all eligible cases, divided into yin and yang, twotrue, phlegm and resistor (a), yang and dampness, phlegm, internal resistance (b), yin deficiency heat, phlegm resistance (c) three.①observation of patients in each group at different dialysis age (≤36months A, B,36to72months,72months C groups) and the primary disease (chronic glomerulonephritis Ⅰ, diabetes Ⅱ, hypertension Ⅲ, other IV four groups), the frequency and distribution characteristics;(2) included in the study compared192cases of patients with renal osteodystrophy, a, b, c three groups of different syndromes of survival quality, and A, B, C, three different groups of patients with dialysis age of survival quality.
     3Results
     3.1Distribution of TCM syndromes in different dialysis ages
     Dialysis age less than36months and dialysis age of the patient population of36to72months of patient population in the yin and yang, yang, yin deficiency group, no significant difference in the distribution. The yin and yang the highest proportion (55.6%) in patients with dialysis age greater than72ROD, the yin and yang type of distribution is relatively small, and no significant difference between the two groups.
     3.2Distribution of TCM syndrome type in different primary diseases
     (1) Primary disease of yin and yang in the group of patients with chronic nephritis the highest proportion (46.8%).(2)Primary disease of yin deficiency in the diabetes group the highest proportion (48.3%), yin and yang, followed by (38.3%), Yang and type at least (13.3%).(3)No significant difference in various types of distributions of the primary disease patients with hypertension.(4)Original incidence of three common complications of syndromes of yin and yang (51.7%), Yang (27.6%), followed by yin deficiency (20.7%) at least.
     3.3Distribution of the primary disease in different ages of the dialysis ROD patients
     With the gradual increase dialysis age growth of the primary disease for patients with chronic glomerulonephritis, diabetic nephropathy in patients gradually reduced the original incidence of hypertension in patients with no obvious regularity.
     3.4The relationship between iPTH and TCM syndrome, dialysis age, primary disease
     Three different TCM syndrome and primary disease in patients with iPTH levels between the two groups were no significant differences (P>0.05); three different groups of patients with dialysis age of serum iPTH levels were significant differences (P values<0.05), and a gradually increasing trend with the dialysis age grew.
     3.5Quality of life of patients with ROD and TCM syndrome
     No significant difference between the physiological function, bodily pain, general health:a group of the worst, b, c group; physiological functions, energy ratings, social functions:a set of the worst, and significant differences compared to b, c (all P<0.01), while b, c group, no significant difference between; feelings of functions:a group no significant difference in b, c, c group than in the group b ideal; mental health:c group the best group b followed by a group of mental health the worst; physical health measurement:the worst group a, b, c compared to the ideal, but between the two groups no significant difference; mental health measurement:a very significant difference among the three groups, and c the best group, followed by group b, a group of the worst; quality of life score evaluation:a group of the worst, b, c compared to the ideal, but there were no significant differences.
     3.6Quality of life of patients with ROD and dialysis age
     Physiological functions, physical function, bodily pain, energy ratings, social functions, group C patients with the worst group A the best; the general state of health:the optimal A, C, followed by B the worst; feelings of functions:the worst A, C, followed by B is best; mental health:the optimal C, followed by B, A, the worst; physical health measurements:A, the best, followed by B, C the worst; mental health measurement:the optimal B, A, times, C the worst; score:B the best, followed by A, C, the worst.
     4Conclusion
     4.1ROD patients with evidence of climate change in line with the trends in the development of the disease law, along with dialysis age and duration of the louder, the yin and yang, phlegm and blood stagnation syndrome is most common that they, and the vacuity of renal osteodystrophy, false is mixed diseasemachine characteristics consistent.
     4.2Primary disease for patients with chronic nephritis ROD common deficiency of both yin and yang, the primary disease is more common yin deficiency and yin and yang deficiency in the diabetic patient population, Yang less card in the primary disease for patients with hypertension designate no significant difference in the distribution of its distribution characteristics to consider with all the original certificates of onset and pathogenesis characteristics can be used as a reference for TCM syndrome differentiation.
     4.3Primary disease was chronic glomerulonephritis in patients with dialysis age longer, and relatively long survival time in patients with diabetic nephropathy, dialysis age shorter survival time is relatively short.
     4.4Quality score of the yin and yang deficiency patients with regard to physical health of each to survive the worst; in the quality of life in mental health, the Yin Deficiency ideal yang type, followed by the yin and yang type worst, kidney-bone law of development of disease pathogenesis, but the yin deficiency type than yang and mental health ideal may yang type in patients with spleen and kidney yang pathogenesis characteristics, the above rules to check against the treatment of Chinese medicine early intervention provides a basis to improve the quality of life in patients.
     4.5The worst quality of life in patients with dialysis age greater than72months with regard to physical health, dialysis age36to72months and patients with less than36months of the worst; quality of life in mental health dialysis aged36to72months in patients with the best, followed by less than36months, the worst of greater than72months.
引文
[1]Moe S, Drueke T,Cunningham J,et al. Definition, evaluation, and classification of renal osteodystrophy.aposition statement from kidney disease:improving global outcomes(KDIGO) [J].Kidney Int,2006,69(11):1945-1953.
    [2]Lopez-Hilker S,GalceranT,Chan YL,et al. Hypercalcemia may not be essential for the development of secondary hyper-parathyoidism in chronic renal failure[J].J Clin Invest,1986,78:1097.
    [3]谢琼虹,丁峰.肾性骨病的药物治疗进展[J].上海医药,2009,30(9):300-302.
    [4]唐荣,唐德.慢性肾脏病患者骨矿物质代谢紊乱的发病机制与治疗的研究进展[J].广东医学院学报,2010,8(2):202-204.
    [5]Levin A, Bakris G L, Molitch M, et al. Prevalence of abnormal serum vitamin D. PTH, calcium, and phosphorus in patients with chronic kidney disease:results of the study to evaluate early kidney disease[J].Kidney Int,2007,71(1):31-38.
    [6]El-KishawiAM, El-NahasAM. Renal osteodystrophy:review of the disease and its treatment[J]. Soudi JKidney Dis Transpl,2006,17(3):373-382.
    [7]曾丽花,李洪.血液透析患者肾性骨病诊治现状[J].医学综述,2009,14(4):578-581.
    [8]Marsell R, Grundberg E, Krajisnik T, et al. Fibroblast growth factor-23 is associated with parathyroid hormone and renal function in a popu-lation-based cohort of elderly men[J]. Eur J Endocrinol,2008,158(1):125-129.
    [9]Riminucci M, Collins M T, Fedarko N S, et al. FGF-23 in fibrousdysplasia of bone and its relationship to renal phosphate wasting[J]. JClin Invest,2003,112(5):683-692.
    [10]Shimada T, HasegawaH, Yamazaki Y, et al. FGF-23 is a potent reg-ulator of vitamin D metabolism and phosphate homeostasis[J]. J BoneMiner Res,2004,19(3):429-435.
    [11]Shimada T,Kakitani M, Yamazaki Y, et al. Targeted ablation of FGF23 demonstrates an essential physiological role of FGF23 in phos-phate and vitamin D metabolism[J]. J Clin Invest,2004,113(4):561-568.
    [12]London G M, Marty C, Marchais S J, et al. Arterial calcifications and bone histomorphometry in end-stage renal disease[J]. J Am SocNephrol,2004,15(7):1943-1951.
    [13]Block G A, Klassen P S, Lazarus J M, et al. Mineral metabolism,mortality, and morbidity in maintenance hemodialysis[J]. J Am So Nephrol,2004,16(7):1853-1861.
    [14]Schoppet M, Shroff R C, Hofbauer L C, et al. Exploring the biology of vascular calcification in chronic kidney disease:what's circulating[J]. Kidney Int,2008,73(4):384-390.
    [15]El-Abbadi M, Giachelli C M. Mechanisms of vascular calcification[J]. Adv Chronic Kidney Dis,2007,14(1):54-66.
    [16]Mathew S, Tustison K S, Sugatani T, et al. The mechanism of phos-phorus as a cardiovascular risk factor in CKD[J]. J Am Soc Nephrol,2008,19(6):1092-1105.
    [17]Ewence A E, Bootman M, Roderick H L, et al. Calcium phosphate crystals induce cell death in human vascular smooth muscle cells:a po-tential mechanism in atherosclerotic plaque destabilization[J]. CircRes,2008,103(5):e28-e34.
    [18]刘富.53例维持性血液透析患者肾性骨病分析[J].海南医学,2010,21(5):63-64.
    [19]张雪.“肾主骨”与肾性骨病的理论初讨[D].硕士学位论文.201O.
    [20]Basile C, Lomonte C, Vernaglione L, et al. A high body mass index and female gender are associated with an increased risk of nodular hyperplasia of parathyroid glands in chronic uraemia[J]. Nephrol Dial Transplant,2006,8:968-974.
    [23]钱莹,陈楠.重视慢性肾脏病中的代谢性骨病[J].诊断学理论与实践,2011,1O(3):214-217
    [24]郑法雷,袁群生.肾性骨病诊治中的新问题及有关进展[J].实用医院临床杂志,2006,3(4):2-5.
    [25]CouttenyeMM, Haese PC, VerschorenWJ, eta.l Low bone turnover in patientwith renal failure[J]. Kidney Int,1999,56(Suppl 73):S70-S76.
    [26]Mucsi I, HerczG..Relative hypoparathyroidism and adynamic bone disease[J]. Am JMed Sci,1999,317(6):405-409.
    [27]Friedman PA, GoodmanWG. PTH(1-84)/PTH(7-84):a balance of power[J]. American Journal of Physiology,2006,289(5):F975-984.
    [29](美)布伦纳(Brenner.B.M).布伦纳-雷克托肾病学[M].第6版.英文影印版.北京:科学出版社,2001.2103-2187.
    [30]申虎威,牛庆寰,杜艳.肾性骨营养不良40例临床分析[J].医学综述,1996,2,(5):219-270
    [31]李广然,余学清.肾性骨病的诊治进展[J].国外医学内科学分册,1998,25(12):515-519.
    [32]Canter T, Sci B. The assay of the hypocal-cemic PTH fragment in hibitor with PTH provides a more accurate assessment of renal osteodystroply ocrnpared to the intact PTH assay. Nefrologia,2003,23 (suppl):69-72.
    [33]赵丽.肾性骨病治疗研究进展[J].河北医药,2009.31(13):1642-1644.
    [34]Alvarez L.T orregrosa JV. Peris P. et al. Effect of he modialysis and renal failure on serum biochemical markers of bone turnover[J].Jbone miner Metab.2004,22(3):254-259.
    [35]张晓雪,刘章锁,唐琳.肾性骨病检测方法研究进展[J].河南职工医学院学报,2010,22(2):244-246.
    [36]张庆怡、牟姗.慢性肾衰竭与肾性骨病[J].中国中西医结合肾病杂志,2003,4(3):125-127.
    [37]Boyce BF, Xing L. Functions of RANKL/RANK/OPG in bone modeling and remodeling[J]. Arch Biochem Biophys.2008;473:139-146.
    [38]Zheng Cai-Mei; Chu Pauling; Wu Chia-Chao; et al. Association between Increased Serum Osteoprotegerin Levels and Improvement in Bone Mineral Density after Parathyroidectomy in Hemodialysis Patients[J].TOHOKU JOURNAL OF EXPERIMENTAL MEDICINE.2012.226.1:(19-27).
    [39]Papadopouli AE, Klonaris CN, Theocharis SE. Role of OPG/RANKL/RANK axis on the vasculature[J].HistolHistopathol,2008,23:497-506.
    [40]Doumouchtsis KK,Kostakis AI,et al. Associations between osteoprotegerin andfemoral neck BMD in hemodialysis patients[J]. J Bone Miner Metab,2008,26:66-72.
    [41]Jiang Jian-Qing; Lin Shan;Xu Peng-Cheng; et al. Serum osteoproteger in measurement for early diagnosis of chronic kidney disease-mineral and bone disorder[J]. NEPHROLOGY,2011,16(6):588-594.
    [42]Chu P,Chao TY, et al.Correlation between histomorpho-metric parametersOfbone resorption and serum type 5b tartrate-resistent acid phosphatase in uremic patients on maintenance he-modialysis[J].Am JKidneyDis,2003,41(5):1052-1059.
    [43]Nakamura M,Fuchinoue S Teraoka S.Clinical experience with percutaneous ethanol injection therapy in hemodialysis patients with renal hyperparathyroidism[J].Am J Kidney Dis.2003,42(4):739-745.
    [44]Cohen-solal ME,Augry F,Mauras Y. et al. Fluoride and strontium accumulation in bone does not correlate with osteoid tissue in dialysis patients [J]. Nephrology, dialysis, transplantation,2002,17(3):449-454.
    [45]成蕊.双能x线骨密度仪对慢性肾衰竭患者骨密度评价[J].中国现代医生,2011.49(21):25-26.
    [46]邓燕,商红.99mTc-MDP骨显像诊断肾性骨病的临床意义[J].中国医学工程,2011.19(5):175-176.
    [47]朱占胜,胡守亮等.肾性骨病检查方法的研究进展[J].实用医学杂志,2010.26(22):4056-4057.
    [48]Floeter Michelle,Floeter Michelle; Bittar Cintia Kelly; Amin Zabeu Jose Luis.Review of comparative studies between bone densitometry and quantitative ultrasound of calcaneus in osteoporosis [J]. Mycoses,2011,36(4):327-335
    [49]Gal-Moscovici A,Sprague S M.Role of bone biopsy in stages 3 to 4 chronic kidney disease[J].Clin J Soc Nephrol,2008,3(3)S170-174.
    [50]Al Badr W,Martin K J.Role of bone biopsy in renal osteodystrophy[J].Saudi J Kidney Dis Transpl,2009,20(1):12-19.
    [51]田寿福,汪年松.透析患者肾性骨病的药物治疗进展[J].医药专论,2011,32(2):93-96.
    [52]张凌.对肾性骨病的治疗会加剧血管钙化吗?[J].中国血液净化,2010.9(5):233-235.
    [53]马迎春,张凌.解读2009KDIGO关于CKD-MBD的诊断、评估及防治临床实践指南[J].中国血液净化,2011.10(5):279-282.
    [54]Noordzii M, Korevaar J C, Boeschoten E W, et al. The Kidney Disease Outcomes Ouality Initiative(K/DOQI) guideline for bone metabolism and disease in CKD:association with mortality in dialysis patients[J]. Am J Kidney Dis,2005,46(5):925-932.
    [55]王小芳,宋亚彬.骨化三醇治疗肾性骨病疗效观察[J].中国实用医药,2011,6(13):84-85.
    [56]Kawata T, Nagano N, Obi M, et al. Cinacalcet suppresses calcification of the aorta and heart in uremic rats[J].Kidney Int,2008,74:1270-1277.
    [57]梁玉环,高鑫等.鲑鱼降钙素对肾性骨病并继发性甲旁亢患者的作用观察[J].药物治疗学.2008,13(8)938-941.
    [58]郑法雷,袁群生.肾-骨对话和肾性骨病:机制与治疗进展[J].中国中西医结合肾病杂志,2008,9(2):95-97.
    [59]李佳.双膦酸盐治疗肾性骨病的研究进展[J].浙江实用医学,2010,15(4):327-328.
    [60]Wetmore JB, Benet LZ, Kleinstuck D, et al. Effects of short-term alendronate on bone mineral density in haemodialysis patients[J]. Nephrology,2005,10(4):393-399.
    [61]Jamal SA, Bauer DC, Ensrud KE, et al. Alendronate treatment in women with normal to severely impaired renal function:an analysis of the fracture intervention trial[J]. J Bone Miner Res,2007,22:503-508.
    [62]Miller PD, Roux C, Boonen S, et al. Safety and efficacy of risedronate in patients with age-related reduced renal function as estimated by the Cockcroft and Gault method:a pooled analysis of nine clinical trials[J]. J Bone MinerRes,2005,20:2105-2115.
    [63]翟建梅.肾性骨病的防治进展[J].中外医疗.2008.9(26):142-143.
    [64]Weisinger JR, Carlini RG, Rojas E, et al. Bone diseaseafter renal transplantation[J]. Clin J Am Soc Nephrol,2006;1:1300-1313.
    [1]Salusky IB,Goodman WG.Cardiovascular calcification in end-stage renal disease[J].Nephrol Dial Transplant,2002,17(2):336-339.
    [2]李小生,唐杨,王茂泓.“肾主骨”与肾性骨病理论探讨[J].江西中医药,2006,37(279):12-13.
    [3]张庆怡,牟姗.慢性肾衰竭与肾性骨病[J].中国中西医结合肾病杂志.2003.4(3):125-127.
    [4]任秀喜,景金霞.健脾补肾食疗法在肾性骨病护理中的应用[J].现代中西医结合杂志.2011,20(35):4572-4573.
    [5]安海燕,任可.补骨汤治疗肾性骨病的临床观察[J].中国中西医结合肾病杂志,2004,5(12):718-719.
    [6]赵玉庸,孙中成,尹雷等.中药复方治疗肾性骨营养不良大鼠的实验研究[J].河北中医学报,2001,16(3):1-3.
    [7]肖相如.肾性骨病的治疗经验[J].辽宁中医杂志,2004,31(2):98-99.
    [8]张宁,李同侠.运用因子分析法研究慢性肾衰肾性骨病中医证候特征初步探讨[J].中华中医药杂志,2008.23(9):794-796.
    [9]吴建华,赵光夸.中医药治疗骨质疏松症研究进展[J].中国中医骨伤科杂志,1995.4(1):56-59.
    [10]赵玉庸,孙中成,尹雷等.中药复方治疗肾性骨营养不良大鼠的实验研究[J].河北中医学报,2001,16(3):1-3.
    [11]白丽娜,李月红.“固本益肾汤”联合骨化三醇治疗肾性骨营养不良临床研究[J].江苏中医药,2010,42(2):20-21.
    [12]关鑫,周家俊,赵东.补肾壮骨汤干预治疗肾性骨病大鼠模型的实验研究[J].中国中西医结合肾病杂志,2003,4(1):10-12.
    [13]许文娟,李秋景,黄雪红,朱良伟.益骨散治疗慢性肾功能不全失代偿期合并肾性骨病20例[J].环球中医药,2011.4(6):473-474.
    [14]李良,刘南梅.补肾健骨汤治疗肾性骨病疗效观察[J].中国中医急症,2008,17(8):1068-1069.
    [15]韩小伟,程淑碧,祁爱蓉,等.针灸与健脾益肾方、罗钙全联用治疗肾性骨病疗效观察[J].中华现代护理杂志,2008,14(11):4-6.
    [16]夏远军,沈霖,谢晶,等.补肾方对成骨细胞生长因子TGF—β1mRNA表达的影响[J].世界骨伤杂志,2005,1(1):82-85.
    [17]郑永明.仙灵骨葆胶囊治疗肾性骨病临床观察及机理探讨[J].中国医疗前.2010.5(22):51,86
    [18]段昱方,赵文景,蔡朕,张胜容.益肾坚骨汤治疗肾性骨病34例临床观察[J].北京中医药.2010.29(9):682-684.
    [19]朱慧峰,王唯佳.骨碎补研究进展[J].中国骨伤,2009,22(1):66-67.
    [20]胡静,郑洪新.牡蛎钙补肾中药复方对骨形成蛋白-4诱导成骨信号转导机制的调控作用[J].中华中医药学刊.2009,27(9):1891-1894.
    [21]石玥,张宁,刘世巍等.补肾活血法治疗肾性骨病60例临床观察[J].北京中医药大学学报.2010.33(11):782-785.
    [22]任秀喜,景金霞,石玉兰,陈秀荣.健脾补肾食疗法在肾性骨病护理中的应用[J].现代中西医结合杂志.2011.20(35):4572-4573.
    [23]黎晓辉,卢叶明,梁艳萍.补肾壮骨汤联合鲑鱼降钙素鼻喷剂治疗肾性骨病的临床研究[J].中西医结合.2008.38(4):134-135.
    [24]吴广文,刘献祥.肾性骨关节炎的辨证施治探讨[J].中医正骨,2007,19(1):74-75.
    [25]任秀喜,景金霞.健脾补肾食疗法在肾性骨病护理中的应用[J].现代中西医结合杂志.2011,20(35):4572-4573.
    [26]郭艳香.第21次中华中医药学会肾病分会学术会议论文汇编[C].北京:中华中医药学会,2008:283-284.
    [1]Moe S,Drueke T,Cunningham J,et al. Definition, evaluation, and classification of renal osteodystrophy.aposition statement from kidney disease:improving global outcomes(KDIGO)[J].Kidney Int,2006,69(11):1945-1953.
    [2]吴广文,刘献祥.肾性骨关节炎的辨证施治探讨[J].中医正骨,2007,19(1):74-75.
    [3]吴建华,赵光夸.中医药治疗骨质疏松症研究进展[J].中国中医骨伤科杂志.1995.4(1):56-59.
    [4]任秀喜,景金霞,石玉兰,陈秀荣.健脾补肾食疗法在肾性骨病护理中的应用[J].现代中西医结合杂志,2011.20(35):4572-4573.
    [5]张宁,李同侠.运用因子分析法研究慢性肾衰肾性骨病中医证候特征初步探讨[J].中华中医药杂志,2008.23(9):794-796.
    [6]中华医学会肾脏病分会透析移植登记工作组.1999年度全国透析移植登记报告[J].中华肾脏病杂志,2001,17(2):77-78.
    [7]贾小军,邢昌赢;肾性骨病PTH检测与组织学检查的临床意义[月.河北医药,2011,33(19):2926-2927.
    [8]Ganesh SK,Stack AQ Levin NW,et al.Association of elevated serum P04,CaxP04product,and parathyroid horm one with cardiac mortality risk in chronic hemodialysis patients[J].JASNL,2001,2:2131-2138.

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