Skip to main content

Characteristics and complications of fracture in older adults with chronic kidney disease: a cross-sectional study

Abstract

Background

The aim of this study was to analyze the clinical characteristics of older fracture patients with chronic kidney disease (CKD) and to determine the risk factors of perioperative cardiovascular complications.

Methods

We retrospectively reviewed clinical data of older fracture patients with CKD admitted to the Third Hospital of Hebei Medical University from January 2016 to October 2021. The data we collected included baseline characteristics and complications. We finally determined the risk factors of perioperative cardiovascular complications by using logistic regression.

Results

We ended up enrolling 224 patients, and there were 91 (40.6%) males and 133 (59.4%) females, with a median age of 79 years. 80–84 years old was the age group with high incidence of fracture. The majority of fracture occurred indoors (130 cases, 58.0%) and morning (98 cases, 43.8%). Hip fracture was most common (183 cases, 81.7%), of which femoral neck fracture (101 cases, 45.0%) was the most prevalent. The most common comorbid condition was hypertension (171 cases, 76.3%), and anemia was the most common complication (148 cases, 66.1%). Age ≥ 80 years (OR = 2.023, 95% CI 1.110–3.688), previously combined with cardiovascular calcification (OR = 1.901, 95% CI 1.047–3.451) and admission hemoglobin level < 100 g/L (OR = 3.191, 95% CI 1.744–5.838) were independent risk factors of perioperative cardiovascular disease (CVD).

Conclusion

It was especially necessary to enhance fracture prevention for CKD. Patients whose age older than 80, hemoglobin less than 100 g/L on admission and have previous cardiovascular calcification are more likely to develop perioperative CVD. Such patients require reasonable decisions during the perioperative period to avoid the occurrence of CVD.

Background

As the population ages, the number of the older over 60 years of age will reach 2 billion by 2050 [1]. Fracture causes serious threats to elderly’s health and life quality. CKD is increasingly common in elderly. With the worsen of kidney function, the fracture rates of the older fallers also increased [2]. Renal osteodystrophy (ROD) has become an important public health problem in the aging societies.

The risk of death after fracture is related to perioperative cardiovascular events [3, 4]. Calcification of blood vessels and valves will cause high risk of CVD among chronic kidney disease patients [5,6,7]. Therefore, cardiovascular calcification will greatly increase the risk of dying from cardiovascular events during the perioperative period among fracture patients with CKD [8, 9].

At present, there are many studies on end-stage renal disease with fracture, but the research on CKD combined with fracture is rare. Therefore, we researched the people with CKD and analyzed their clinical characteristics and the risk factors of CVD.

Methods

Patients and groups

This was a retrospective study of 224 adults over 65 years of age with fracture and previous CKD who were hospitalized in the Third Hospital of Hebei Medical University from January 2016 to October 2021. This study was declaration of Helsinki compliant, and the Institutional Review Committee of the Third Hospital of Hebei Medical University supported us in doing this research. Since this is a retrospective study, we gave up the informed consent of the respondents and protected the confidentiality of them by anonymizing their data.

The collected data of interest included demographic data such as gender and age, the characteristics of fracture and the complications in the perioperative period. From 65 to 100 years, patients were divided into seven age groups at intervals of 5 years. The time of fracture occurrence was recorded as dawn (0:00–6:00), morning (6:00–12:00), afternoon (12:00–18:00) and night (18:00–24:00). The place where the fracture occurred included indoor and outdoor. The fracture types were divided into hip (femoral neck, intertrochanter) and non-hip fracture.

Inclusion and exclusion criteria

Inclusion criteria were as follows: (1) 65 years of age or older; (2) with a previous diagnosis of CKD; (3) with a definite diagnosis of fracture by imaging; (4) with complete data.

Exclusion criteria were as follows: (1) high energy trauma fracture (car accident, fall from height, etc.); (2) old fracture; (3) long-term administration of glucocorticoids or selective estrogen receptor modulators; (4) have a history of diseases that affect bone metabolism, such as tuberculosis, malignant tumors, and Cushing’s syndrome.

There were two orthopedic physicians and one internal medicine physician forming an investigation team. Two orthopedic doctors performed the image reading. The agreement between the two orthopedic doctors was 95%. The internal medicine physician conducted quality control and regularly conducted sampling inspections on the reading results.

Disease definition

The diagnosis of cardiovascular calcification was based on chest radiography to detect aortic and coronary calcification, and cardiac ultrasound to detect calcification of heart valves. If the patient has calcification in at least one examination site, the patient was assessed as having cardiovascular calcification: mitral valve, aortic valve, aorta, or coronary artery [10, 11].

Statistical analysis

Data were analyzed by IBM SPSS Statistics version 25.0, and the statistically significant level was set at P < 0.05. All data are based on Kolmogorov–Smirnoff to test for normality. We used the mean ± standard deviation to represent the data that conformed to the normal distribution, and non-normally distributed variables were represented by the median and interquartile range. Two sample Welch t test or nonparametric test was used for continuous variables, and Chi-square or nonparametric test for categorical variables. Categorical variables were expressed in frequency and percentage. The data with a P < 0.10 were analyzed with logistic regression.

Results

Baseline characteristics

From January 2016 to October 2021, 224 fracture patients with CKD who satisfy the inclusion criteria were enrolled in the study. These patients included 133 (59.4%) women and 91 (40.6%) men, with a median age of 79 years. The most common age group was 80–84 years old, with a total of 51 cases (22.8%). A total of 171 patients were presenting with hypertension, accounting for 76.3%, other comorbidities included cardiovascular calcification (47.8%), chronic heart failure (46.9%), diabetes (42.0%) and old cerebral infarction (38.8%). Of the 224 patients, 49 (21.9%) from dialysis patients, and 175 (78.1%) from patients received no dialysis. CKD stage 5 (78, 34.8%) and CKD stage 3 (78, 34.8%) patients accounted for the highest proportion (Table 1).

Table 1 Baseline characteristics of elderly patients with CKD and fracture

The age groups distribution of dialysis and non-dialysis patients was different statistically (P < 0.05). The most prevalent age group of dialysis patients was 65–69 years, and 80–84 years was the predominant age group of non-dialysis patients. The specific distribution of characteristics can be seen in Fig. 1.

Fig. 1
figure 1

Composition of age and history of dialysis in elderly patients with CKD and fracture

Place and time of fracture occurrence, and types of hip fracture

Among the data when and where fracture occurred, most patients developed nine fracture indoors (130 cases, 58.0%) and in the morning (98 cases, 43.8%). There were 101 (45.0%) femoral neck fracture and 82 (36.6%) femoral intertrochanteric fracture (Table 2).

Table 2 The distribution of place, time of fracture occurrence and type of hip fracture

Perioperative complications

Patients with anemia in the perioperative period accounted for the highest proportion (148 cases,66.1%) .147 cases (65.6%) with cardiovascular complications, of which acute heart failure was the most frequent (122 cases, 54.5%), followed by arrhythmia (62 cases, 27.7%) and myocardial infarction (19 cases, 8.5%). Other complications included hypoalbuminemia (112 cases, 50.0%), deep vein thrombosis of the lower extremities (78 cases, 34.8%), electrolyte disorder (72 cases, 32.1%), serous cavity effusion (45 cases, 20.1%) and pulmonary infection (41 cases, 18.3%) (Table 3).

Table 3 Perioperative complications of patients with CKD and fracture

Analysis of risk factors of CVD

The differences between the patients with and without CVD during the perioperative period are shown in Table 4. Factors including age, types of fracture, combined with cardiovascular calcification, and hemoglobin on admission were P < 0.1. The logistic regression showed that age ≥ 80 years (OR = 2.023, CI = 1.110–3.688, p = 0.021), previous combined with cardiovascular calcification (OR = 1.901, CI = 1.047–3.451, p = 0.035) and hemoglobin on admission < 100 g/L (OR = 3.191, CI = 1.744–5.838, p = 0.000) were important independent risk factors of perioperative CVD in fracture patients with CKD (Table 5).

Table 4 The association of CVD with gender, age, fracture location, comorbidities, and number of hemoglobin on admission
Table 5 Multivariate analysis of preoperative variables associated with CVD (multinomial logistic regression; (Enter)

Discussion

In our study of 224 older adults, we examined characteristics and complications of fracture of patients with CKD. We have found that elderly CKD with fracture was more common in women, 80–84 years old, and people with hypertension. Dialysis patients combined with fracture were more common in younger age groups. Patients with CKD stage 5 had the highest rates of fracture. The type of fracture was mainly hip fracture. Most patients had fracture indoors and in the morning. Anemia accounted for the highest proportion of perioperative complications. Risk factors of CVD in the perioperative period consisted of age ≥ 80 years old, previous combined cardiovascular calcification, and hemoglobin < 100 g/L on admission.

We concluded that the number of women suffered from fracture was more than that of men, and the result was the same as the conclusion of some research works [12]. In addition to the reduced estrogen during menopause, the female CKD patients more commonly have high parathyroid hormone (PTH), leading to loss of cortical bone [13]. There is also evidence that women are more susceptible to CKD [14] and women are an independent risk factor for fracture in hemodialysis patients [15]. Therefore, in CKD patients with fracture, the result that there are more women than men is no exception [16]. Among the patients, we included 80–84 years old CKD with fracture accounted for the largest proportion. As early as the results of a large population study in the USA from 1985 to 2005, it was concluded that the common age of renal failure with hip fracture was 75–84 years. This result overlapped with our results [17]. Most studies believed that advancing age was the driver for the increase in incidence rates of fracture [18, 19]. However, in our study, dialysis patients combined with fracture were more common in younger age groups compared with non-dialysis patients, which might be related to the worse kidney function of dialysis patients, the decline in the function of various organs of the body and the deterioration of life activity ability. As a result, younger dialysis patients were prone to low-energy falls and hip fracture. For such patients, regardless of age, we cannot relax our vigilance.

Across all comorbidities, hypertension accounted for the highest proportion. This was due to the fact that hypertension is one of the most frequent underlying disorders of the elderly. The loss of urinary calcium leads to a decrease in bone quality, and when blood pressure fluctuates, it is easy to cause dizziness and increase the risk of falls [4]. It has also been suggested that patients with hypertension will experience a decrease in calcium bone absorption when treated with calcium channel blockers [20] and a risk factor for falls from orthostatic hypotension when treated with Angiotensin-converting enzyme inhibitor (ACEI) [21]. Our findings indicated that chronic heart failure was the second most common comorbidity, with a total of 105 cases. The conclusion had been verified in Gere Sunder-Plassmann’s research [22, 23]. Growing evidence shows that diabetes mellitus will increase the risk of fracture after a fall, and it may be related to the transient amaurosis or dizziness [24,25,26,27]. In our study, patients with CKD stage 5 had the highest rates of fracture (78, 34.8%). The risk of hip fracture increased with severity of kidney diseases [2, 7, 28, 29]. Some researchers have also confirmed that the prevalence of renal failure combined with fracture is as high as 98% in dialysis patients and 84% in CKD3-5 stages [5]. Therefore, patients with severe chronic renal insufficiency are more likely to have ROD.

In our study, elderly people with CKD were more likely to develop fracture indoors and in the morning. One plausible explanation is that dialysis treatment maintains renal function, but also causes physical weakness by the loss of amino acids and other nutrients during dialysis, finally causes skeletal muscle weakness, dizziness, fatigue or slow gait speed and restrict patients’ range of activities indoors in order to avoid outdoor unsafe factors [30, 31]. Another reason that can be explained is CKD patient usually suffers from restless legs syndrome. The calf often feels uncomfortable at night, which causes the patient to overactive at dawn or in the morning to relieve leg pain, and ultimately increase the risk of falling. Therefore, for the older adults with CKD, they should have as many escorts around them as possible, using crutches, guardrails and other measures to prevent falls and keep the floor in the home and the dialysis room dry and tidy. We also showed that hip fracture was the most common type, and most studies have yielded same results [32]. One of the possible explanations of this is people with a higher risk of fracture often have poor neuromuscular function [33, 34]. Moreover, the cross-sectional area of the vastus lateralis muscles will be substantially reduced in the elderly, thus increasing the incidence of hip fracture [35]. In addition, the hip as a long-term weight-bearing site makes the bone more vulnerable to damage, and the hip is usually used as the stress point when most patients fall.

Anemia occupied the highest proportion of perioperative complications in our study, which is related to the reduction in erythropoietin and myelosuppression caused by the long-term accumulation of metabolic waste. In addition, hip fracture as the most common fracture location leads to massive blood loss [36]. Although, in our study, anemia was studied as a perioperative complication, analysis of our data confirmed patients who had hemoglobin on admission < 100 g/L had increased the incidence of CVD. Therefore, long-term chronic anemia can be used to explain other complications, especially the cardiovascular system. Seydou Sy et al. pointed out in the latest study in 2021 that anemia was closely related to myocardial hypertrophy [37]. As CKD patients are often complicated with sodium and water retention in the body, chronic anemia and hypoxia, the heart has a long-term compensatory function to ensure sufficient oxygen supply to the peripheral circulation. Overload of the heart and myocardial hypertrophy will ultimately increase the risks of heart failure and myocardial infarction in the perioperative period. They accounted for 54.5% and 8.5% in our data, respectively. Conversely, heart failure leads to decreased renal perfusion and exacerbates renal failure. Anemia, an important factor in aggravating heart and renal failure, will lead to tissue hypoxia, peripheral vasodilation, sympathetic nervous system and RAAS system excitation and constrict renal blood vessels, aggravate myocardial oxygen consumption. Heart failure, renal failure and anemia activate each other, creating a vicious cycle of damage [38]. So some scholars have proposed that chronic anemia is one of several risk factors of cardiac complications [22] and the concept of cardiorenal anemia syndrome [38, 39].

CKD leads to congestive heart failure by increasing sodium and water retention in the body. Anemia will lead to tissue hypoxia, peripheral vasodilation, sympathetic nervous system and RAAS system excitation and constrict renal blood vessels, aggravate myocardial oxygen consumption, and become an important factor in aggravating heart and renal failure. Heart failure, renal failure and anemia activates each other, creating a vicious cycle of damage.

Many investigators have confirmed that cardiovascular event is the main cause of death in patients with CKD [40, 41]. When the kidney function stage is lower than CKD stage 2, the risk of cardiovascular events will increase as the stages of renal failure increase [42,43,44]. Hypertension as the most common comorbidities causes the decrease in left ventricular function by increasing cardiac afterload and myocardial oxygen consumption, which ultimately makes patients suffer from high incidence of cardiovascular complications. Therefore, for patients with CKD after traumatic stress, surgeons not only need to solve the problem of fracture, but also deal with the underlying diseases that can cause perioperative complications, such as correcting anemia on admission and controlling hypertension [44]. CKD is a leading contributor to electrolyte disturbance, and electrolyte disturbance is the leading underlying cause of arrhythmia. High extracellular potassium causes prolongation of the action potential duration, which makes the heart more prone to bradyarrhythmias, such as sinus arrest, sinus bradycardia, and ventricular fibrillation [45]. Therefore, correcting serum electrolyte disturbance from the decline of renal function is still the key to reducing perioperative complications in patients with fracture.

Cardiovascular calcification is common among healthy elderly. All arteries can be calcified especially small arteries in hemodialysis patients [45, 46]. This is because patients with CKD are usually accompanied by abnormalities in blood calcium, blood phosphorus, PTH and other bone metabolism indicators [47]. In patients with early renal insufficiency, the fibroblast growth factor-23 (FGF-23) produced by bone cells can be increased, which can inhibit the production of PTH, reduce the absorption of calcium and phosphorus in the intestine, and pass Klotho synergistic action to promote the effect of urinary phosphorus excretion [48]. Blood phosphorus in patients with early renal failure is usually in the normal range, but as renal function deteriorates, the lack of kidney Klotho will reduce the effect of FGF-23 in inhibiting PTH, on the one hand, and eventually lead to excessive release of PTH, which accelerates bone resorption, and intracellular Ca overload ultimately accelerates cardiovascular calcification [48]. On the other hand, as the kidney’s ability to excrete phosphorus decreases, blood phosphorus will counteract the effect of FGF-23 and gradually become higher than normal [49, 50] and induce vascular calcification by activating pro-inflammatory molecules in vascular smooth muscle cells [47]. In addition, FGF23 and Klotho themself are also related to vascular calcification. Klotho has a protective effect against calcification, and its defects in CKD will accelerate cardiovascular calcification [51]. FGF23 is an inhibitor of vascular calcification [52]. In addition, some researchers found decreased bone mass and extensive vascular calcification in mice knocking out FGF23 and Klotho genes. This fact also strengthened the view that there is a common pathway between bone and vascular metabolism [53]. Even the patients with earlier stages of CKD and with normal renal function, vascular calcification can lead to cardiovascular events, shorten life expectancy, and increase mortality [54]. Therefore, for older patients with CKD, surgeons routinely perform chest and abdomen X-rays and echocardiography after the patient being admitted to the hospital, which can effectively detect the degree of calcification of blood vessels and valves, and avoid perioperative CVD.

The fracture elderly with CKD is still a large group. Our data showed that it is important for clinicians to make reasonable decisions in the perioperative management of fracture patients with CKD and avoid the occurrence of perioperative CVD.

Limitations

First of all, the collection of retrospectively designed data has certain limitations. For example, it is not completely accurate for us to use clinical information collected by one hospital to infer the overall clinical characteristics. Secondly, we collected patients who did not choose dialysis because of subjective factors. In addition, we lack some meaningful indicators, such as bone density, parathyroid hormone and vitamin D collection. At the same time, we have no statistics on the perioperative medications and surgical treatment methods of all the participants.

Conclusion

Our research results emphasize the need to enhance fracture prevention for CKD patients. Particular attention should be paid to avoiding CVD during the perioperative period for patients whose age older than 80, hemoglobin less than 100 g/L on admission and have previous cardiovascular calcification.

Availability of data and materials

The data used to support the findings of this study are available from Zhiqian Wang upon request.

References

  1. Boe DM, Boule LA, Kovacs EJ. Innate immune responses in the ageing lung. Clin Exp Immunol. 2017;187(1):16–25.

    Article  CAS  PubMed  Google Scholar 

  2. Bowling CB, Plantinga L, Phillips LS, McClellan W, Echt K, Chumbler N, et al. Association of multimorbidity with mortality and healthcare utilization in chronic kidney disease. J Am Geriatr Soc. 2017;65(4):704–11.

    Article  PubMed  Google Scholar 

  3. Li C, Chen XM, Li Y, Zhou YL, Yan JN, Du XG. Factors and outcome of renal osteodystrophy-associated initial fragility fracture in end-stage renal disease patients. Kidney Dis (Basel). 2019;5(2):118–25.

    Article  Google Scholar 

  4. Xie L, Hu X, Li W, Ouyang Z. A retrospective study of end-stage kidney disease patients on maintenance hemodialysis with renal osteodystrophy-associated fragility fractures. BMC Nephrol. 2021;22(1):23.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  5. KDIGO clinical practice guideline for the diagnosis, evaluation, prevention, and treatment of Chronic Kidney Disease-Mineral and Bone Disorder (CKD-MBD). Kidney Int Suppl. 2009(113):S1–130.

  6. Spasovski GB. Bone biopsy as a diagnostic tool in the assessment of renal osteodystrophy. Int J Artif Organs. 2004;27(11):918–23.

    Article  CAS  PubMed  Google Scholar 

  7. Pimentel A, Urena-Torres P, Bover J, Luis Fernandez-Martin J, Cohen-Solal M. Bone fragility fractures in CKD patients. Calcif Tissue Int. 2021;108(4):539–50.

    Article  CAS  PubMed  Google Scholar 

  8. Masumoto A, Sonou T, Ohya M, Yashiro M, Nakashima Y, Okuda K, et al. Calcium overload accelerates phosphate-induced vascular calcification via pit-1, but not the calcium-sensing receptor. J Atheroscler Thromb. 2017;24(7):716–24.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  9. Thiem U, Soellradl I, Robl B, Watorek E, Blum S, Dumfarth A, et al. The effect of phosphate binder therapy with sucroferric oxyhydroxide on calcification propensity in chronic haemodialysis patients: a randomized, controlled, crossover trial. Clin Kidney J. 2021;14(2):631–8.

    Article  CAS  PubMed  Google Scholar 

  10. Rroji M, Seferi S, Cafka M, Likaj E, Cadri V, Barbullushi M. MO570Pulse pressure: a predictor of cardiovascular calcification and cardiovascular mortality in hemodialysis patients. Nephrol Dialy Transplant. 2021;36(Supplement_1):gfab086-008.

    Article  Google Scholar 

  11. You AYF, Bergholt MS, St-Pierre JP, Kit-Anan W, Pence IJ, Chester AH, et al. Raman spectroscopy imaging reveals interplay between atherosclerosis and medial calcification in the human aorta. Sci Adv. 2017;3(12):e1701156.

    Article  PubMed  PubMed Central  Google Scholar 

  12. Lin R, Toussaint ND, Gallagher M, Cass A, Kotwal S. Hospitalized fracture rates amongst patients with chronic kidney disease in Australia using data linkage. Nephrology (Carlton). 2020;25(6):475–82.

    Article  Google Scholar 

  13. Pimentel A, Ureña-Torres P, Zillikens MC, Bover J, Cohen-Solal M. Fractures in patients with CKD-diagnosis, treatment, and prevention: a review by members of the European Calcified Tissue Society and the European Renal Association of Nephrology Dialysis and Transplantation. Kidney Int. 2017;92(6):1343–55.

    Article  PubMed  Google Scholar 

  14. Hill NR, Fatoba ST, Oke JL, Hirst JA, O’Callaghan CA, Lasserson DS, et al. Global prevalence of chronic kidney disease: a systematic review and meta-analysis. PLoS ONE. 2016;11(7):e0158765.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  15. Matias PJ, Laranjinha I, Azevedo A, Raimundo A, Navarro D, Jorge C, et al. Bone fracture risk factors in prevalent hemodialysis patients. J Bone Miner Metab. 2020;38(2):205–12.

    Article  CAS  PubMed  Google Scholar 

  16. Hampson G, Elder GJ, Cohen-Solal M, Abrahamsen B. A review and perspective on the assessment, management and prevention of fragility fractures in patients with osteoporosis and chronic kidney disease. Endocrine. 2021;73(3):509–29.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  17. Roy D, Pande S, Thalanki S, Yeon W, Prasad A, Lau A, et al. Hip fractures in elderly patients with non-dialysis dependent chronic kidney disease: outcomes in a Southeast Asian population. Medicine (Baltimore). 2021;100(27):e26625.

    Article  CAS  Google Scholar 

  18. Lorentzon M, Nilsson AG, Johansson H, Kanis JA, Mellstrom D, Sundh D. Extensive undertreatment of osteoporosis in older Swedish women. Osteoporos Int J Establ Result Cooperation Between Eur Found Osteoporos Natl Osteoporos Found USA. 2019;30(6):1297–305.

    Article  CAS  Google Scholar 

  19. Banefelt J, Akesson KE, Spangeus A, Ljunggren O, Karlsson L, Strom O, et al. Risk of imminent fracture following a previous fracture in a Swedish database study. Osteoporos Int J Establ Result Cooperation Between Eur Found Osteoporos Natl Osteoporos Found USA. 2019;30(3):601–9.

    Article  CAS  Google Scholar 

  20. Fouquoire B, Poncelet P, Warembourg A, Petetin N, Debrueres S, Carre A. Calcium intestinal absorption in normotensive and essential hypertensive subjects before and after nicardipine. Arch Mal Coeur Vaiss. 1989;82(7):1289–91.

    CAS  PubMed  Google Scholar 

  21. Goto NA, Weststrate ACG, Oosterlaan FM, Verhaar MC, Willems HC, Emmelot-Vonk MH, et al. The association between chronic kidney disease, falls, and fractures: a systematic review and meta-analysis. Osteoporos Int J Establ Result Cooperation Between Eur Found Osteoporos Natl Osteoporos Found USA. 2020;31(1):13–29.

    Article  CAS  Google Scholar 

  22. Sunder-Plassmann G, Horl WH. Effect of erythropoietin on cardiovascular diseases. Am J Kidney Dis. 2001;38(4 Suppl 1):S20–5.

    Article  CAS  PubMed  Google Scholar 

  23. Huang Y, Wang S, Zhou J, Liu Y, Du C, Yang K, et al. IRF1-mediated downregulation of PGC1alpha contributes to cardiorenal syndrome type 4. Nat Commun. 2020;11(1):4664.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  24. Deandrea S, Lucenteforte E, Bravi F, Foschi R, La Vecchia C, Negri E. Risk factors for falls in community-dwelling older people: a systematic review and meta-analysis. Epidemiology. 2010;21(5):658–68.

    Article  PubMed  Google Scholar 

  25. Jansen S, Bhangu J, de Rooij S, Daams J, Kenny RA, van der Velde N. The association of cardiovascular disorders and falls: a systematic review. J Am Med Dir Assoc. 2016;17(3):193–9.

    Article  PubMed  Google Scholar 

  26. Atsumi K, Kushida K, Yamazaki K, Shimizu S, Ohmura A, Inoue T. Risk factors for vertebral fractures in renal osteodystrophy. Am J Kidney Dis. 1999;33(2):287–93.

    Article  CAS  PubMed  Google Scholar 

  27. Vestergaard P. Discrepancies in bone mineral density and fracture risk in patients with type 1 and type 2 diabetes–a meta-analysis. Osteoporos Int J Establ Result Cooperation Between Eur Found Osteoporos Natl Osteoporos Found USA. 2007;18(4):427–44.

    Article  CAS  Google Scholar 

  28. Vilaca T, Salam S, Schini M, Harnan S, Sutton A, Poku E, et al. Risks of hip and nonvertebral fractures in patients with CKD G3a–G5D: a systematic review and meta-analysis. Am J Kidney Dis. 2020;76(4):521–32.

    Article  PubMed  Google Scholar 

  29. Kim SH, Yi SW, Yi JJ, Kim YM, Won YJ. Chronic kidney disease increases the risk of hip fracture: a prospective cohort study in Korean adults. J Bone Miner Res Off J Am Soc Bone Miner Res. 2020;35(7):1313–21.

    Article  CAS  Google Scholar 

  30. Lin YL, Hsu BG. Assessment of uremic sarcopenia in dialysis patients: an update. Tzu Chi Med J. 2022;34(2):182–91.

    Article  PubMed  Google Scholar 

  31. Kalantar-Zadeh K, Ikizler TA, Block G, Avram MM, Kopple JD. Malnutrition-inflammation complex syndrome in dialysis patients: causes and consequences. Am J Kidney Dis. 2003;42(5):864–81.

    Article  PubMed  Google Scholar 

  32. Maravic M, Ostertag A, Urena P, Cohen-Solal M. Dementia is a major risk factor for hip fractures in patients with chronic kidney disease. Osteoporos Int J Establ Result Cooperation Between Eur Found Osteoporos Natl Osteoporos Found USA. 2016;27(4):1665–9.

    Article  CAS  Google Scholar 

  33. Obi Y, Hamano T, Isaka Y. Prevalence and prognostic implications of vitamin D deficiency in chronic kidney disease. Dis Markers. 2015;2015:868961.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  34. Elder GJ. Vitamin D levels, bone turnover and bone mineral density show seasonal variation in patients with chronic kidney disease stage 5. Nephrology (Carlton). 2007;12(1):90–4.

    CAS  Google Scholar 

  35. Kalyani RR, Corriere M, Ferrucci L. Age-related and disease-related muscle loss: the effect of diabetes, obesity, and other diseases. Lancet Diabetes Endocrinol. 2014;2(10):819–29.

    Article  PubMed  PubMed Central  Google Scholar 

  36. Brink O. Hip fracture clearance: how much optimisation is necessary? Injury. 2020;51(Suppl 2):S111–7.

    Article  PubMed  Google Scholar 

  37. Sy S, Samaké M, Fofana AS, Diallo A, Coulibaly M, Sy D, et al. Prevalence of severe anemia (Hb ≤ 5 g/dl) in non-dialyzed chronic renal failure patients in the nephrology and hemodialysis department of point G university hospital. Open J Nephrol. 2021;11(02):252–64.

    Article  Google Scholar 

  38. McCullough PA. Anemia of cardiorenal syndrome. Kidney Int Suppl. 2021;11(1):35–45.

    Article  Google Scholar 

  39. Mathew J, Katz R, St John Sutton M, Dixit S, Gerstenfeld EP, Ghio S, et al. Chronic kidney disease and cardiac remodelling in patients with mild heart failure: results from the REsynchronization reVErses Remodeling in Systolic Left vEntricular Dysfunction (REVERSE) study. Eur J Heart Fail. 2012;14(12):1420–8.

    Article  PubMed  PubMed Central  Google Scholar 

  40. Sarnak MJ, Levey AS, Schoolwerth AC, Coresh J, Culleton B, Hamm LL, et al. Kidney disease as a risk factor for development of cardiovascular disease: a statement from the American Heart Association Councils on kidney in cardiovascular disease, high blood pressure research, clinical cardiology, and epidemiology and prevention. Circulation. 2003;108(17):2154–69.

    Article  PubMed  Google Scholar 

  41. Okabe T, Yakushiji T, Kido T, Kimura T, Asukai Y, Shimazu S, et al. Poor prognosis of heart failure patients with in-hospital worsening renal function and elevated BNP at discharge. ESC Heart Fail. 2020;7(5):2912–21.

    Article  PubMed  PubMed Central  Google Scholar 

  42. Gansevoort RT, Correa-Rotter R, Hemmelgarn BR, Jafar TH, Heerspink HJ, Mann JF, et al. Chronic kidney disease and cardiovascular risk: epidemiology, mechanisms, and prevention. Lancet (London, England). 2013;382(9889):339–52.

    Article  Google Scholar 

  43. Afsar B, Rossignol P, van Heerebeek L, Paulus WJ, Damman K, Heymans S, et al. Heart failure with preserved ejection fraction: a nephrologist-directed primer. Heart Fail Rev. 2017;22(6):765–73.

    Article  PubMed  Google Scholar 

  44. Smith DH, Thorp ML, Gurwitz JH, McManus DD, Goldberg RJ, Allen LA, et al. Chronic kidney disease and outcomes in heart failure with preserved versus reduced ejection fraction: the cardiovascular research network PRESERVE study. Circ Cardiovasc Qual Outcomes. 2013;6(3):333–42.

    Article  PubMed  PubMed Central  Google Scholar 

  45. Pochineni V, Rondon-Berrios H. Electrolyte and acid-base disorders in the renal transplant recipient. Front Med (Lausanne). 2018;5:261.

    Article  Google Scholar 

  46. Leu HJ, Brunner U. Calcified and ossified phlebosclerosis. VASA Z Gefasskrankheiten. 1992;21(1):11–4.

    CAS  Google Scholar 

  47. Shanahan CM, Crouthamel MH, Kapustin A, Giachelli CM. Arterial calcification in chronic kidney disease: key roles for calcium and phosphate. Circ Res. 2011;109(6):697–711.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  48. Cai ZY, Hu XF, Chen LQ, Li ZR, Du XG. A cross-sectional study of osteoporosis and cardiovascular calcification in patients with chronic kidney disease at different CKD stages. Sichuan Da Xue Xue Bao Yi Xue Ban. 2021;52(2):334–9.

    PubMed  Google Scholar 

  49. Gross P, Six I, Kamel S, Massy ZA. Vascular toxicity of phosphate in chronic kidney disease: beyond vascular calcification. Circ J. 2014;78(10):2339–46.

    Article  CAS  PubMed  Google Scholar 

  50. Vervloet MG, Sezer S, Massy ZA, Johansson L, Cozzolino M, Fouque D. The role of phosphate in kidney disease. Nat Rev Nephrol. 2017;13(1):27–38.

    Article  CAS  PubMed  Google Scholar 

  51. Reiss AB, Miyawaki N, Moon J, Kasselman LJ, Voloshyna I, D’Avino R Jr, et al. CKD, arterial calcification, atherosclerosis and bone health: inter-relationships and controversies. Atherosclerosis. 2018;278:49–59.

    Article  CAS  PubMed  Google Scholar 

  52. Parker BD, Schurgers LJ, Brandenburg VM, Christenson RH, Vermeer C, Ketteler M, et al. The associations of fibroblast growth factor 23 and uncarboxylated matrix Gla protein with mortality in coronary artery disease: the Heart and Soul Study. Ann Intern Med. 2010;152(10):640–8.

    Article  PubMed  PubMed Central  Google Scholar 

  53. Memon F, El-Abbadi M, Nakatani T, Taguchi T, Lanske B, Razzaque MS. Does Fgf23-klotho activity influence vascular and soft tissue calcification through regulating mineral ion metabolism? Kidney Int. 2008;74(5):566–70.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  54. Cannata-Andia JB, Martin-Carro B, Martin-Virgala J, Rodriguez-Carrio J, Bande-Fernandez JJ, Alonso-Montes C, et al. Chronic kidney disease-mineral and bone disorders: pathogenesis and management. Calcif Tissue Int. 2021;108(4):410–22.

    Article  CAS  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Contributions

All authors read and approved the final manuscript.

Corresponding authors

Correspondence to Zhiqian Wang or Yingze Zhang.

Ethics declarations

Ethical approval and informed consent

This retrospective study was approved by the institutional review board of the third Hospital of Hebei Medical University. To protect patient privacy, the informed consent requirement was waived and our data are collected anonymously.

Competing interests

The authors declare that there is no conflict of interest regarding the publication of this paper.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Meng, Y., Fu, M., Guo, J. et al. Characteristics and complications of fracture in older adults with chronic kidney disease: a cross-sectional study. J Orthop Surg Res 17, 377 (2022). https://doi.org/10.1186/s13018-022-03253-8

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s13018-022-03253-8

Keywords