Obesity and Kidney Disease: Hidden Consequences of the Epidemic

Review Article

Austin J Nephrol Hypertens. 2016; 3(2): 1062.

Obesity and Kidney Disease: Hidden Consequences of the Epidemic

Kovesdy CP1,2*, Furth S³ and Zoccali C4

¹Department of Medicine, University of Tennessee Health Science Center, USA

²Nephrology Section, Memphis VA Medical Center, USA

³Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, USA

4CNR - IFC Clinical Epidemiology and Pathophysiology of Renal Diseases and Hypertension, Italy

*Corresponding author: Csaba Kovesdy, Department of Medicine, University of Tennessee Health Science Center, USA

Received: October 05, 2016; Accepted: December 16, 2016; Published: December 19, 2016

Abstract

Obesity has become a worldwide epidemic, and its prevalence has been projected to grow by 40% in the next decade. This increasing prevalence has implications for the risk of diabetes, cardiovascular disease and also for Chronic Kidney Disease. A high body mass index is one of the strongest risk factors for new-onset Chronic Kidney Disease. In individuals affected by obesity, a compensatory hyperfiltration occurs to meet the heightened metabolic demands of the increased body weight. The increase in intraglomerular pressure can damage the kidneys and raise the risk of developing Chronic Kidney Disease in the long-term. The incidence of obesity-related glomerulopathy has increased ten-fold in recent years. Obesity has also been shown to be a risk factor for nephrolithiasis, and for a number of malignancies including kidney cancer. This year the World Kidney Day promotes education on the harmful consequences of obesity and its association with kidney disease, advocating healthy lifestyle and health policy measures that makes preventive behaviors an affordable option.

Keywords: Obesity; Chronic kidney disease; Nephrolithiasis; Kidney cancer; Prevention

Introduction

In 2014, over 600 million adults worldwide, 18 years and older, were obese. Obesity is a potent risk factor for the development of kidney disease. It increases the risk of developing major risk factors for Chronic Kidney Disease (CKD), like diabetes and hypertension, and it has a direct impact on the development of CKD and end-stage renal disease (ESRD). In individuals affected by obesity, a (likely) compensatory mechanism of hyperfiltration occurs to meet the heightened metabolic demands of the increased body weight. The increase in intraglomerular pressure, along with numerous other mechanisms directly or indirectly linked to obesity (see below) can damage the kidney structure and raise the risk of developing CKD in the long-term.

The good news is that obesity, as well as the related CKD, are largely preventable. Education and awareness of the risks of obesity and a healthy lifestyle, including proper nutrition and exercise, can dramatically help in preventing obesity and kidney disease. This article reviews the association of obesity with kidney disease on the occasion of the 2017 World Kidney Day.

Epidemiology of obesity in adults and children

Over the last 3 decades, the prevalence of overweight and obese adults (BMI =25 kg/m2) worldwide has increased substantially [1]. In the US, the age-adjusted prevalence of obesity in 2013-2014 was 35% among men and 40.4% among women [2]. The problem of obesity also affects children. In the US in 2011-2014, the prevalence of obesity was 17% and extreme obesity 5.8% among youth 2-19 years of age. The rise in obesity prevalence is also a worldwide concern [3,4], as it is projected to grow by 40% across the globe in the next decade. Low- and middle-income countries are now showing evidence of transitioning from normal weight to overweight and obesity as parts of Europe and the United States did decades ago [5]. This increasing prevalence of obesity has implications for cardiovascular disease (CVD) and also for CKD. A high body mass index (BMI) is one of the strongest risk factors for new-onset CKD [6,7].

Definitions of obesity are most often based on BMI (i.e. weight [kilograms] divided by the square of his or her height [meters]). A BMI between 18.5 and 25 kg/m2 is considered by the World Health Organization (WHO) to be normal weight, a BMI between 25 and 30 kg/m2 as overweight, and a BMI of >30 kg/m2 as obese. Although BMI is easy to calculate, it is a poor estimate of fat mass distribution, as muscular individuals or those with more subcutaneous fat may have a BMI as high as individuals with larger intraabdominal (visceral) fat. The latter type of high BMI is associated with substantially higher risk of metabolic and cardiovascular disease. Alternative parameters to more accurately capture visceral fat include waist circumference (WC) and a waist hip ratio (WHR) of >102 cm and 0.9, respectively, for men and >88 cm and >0.8, respectively, for women. WHR has been shown to be superior to BMI for the correct classification of obesity in CKD [7-9].

Association of obesity with CKD and other renal complications

Numerous population based studies have shown an association between measures of obesity and both the development and the progression of CKD (Table 1). Higher BMI is associated with the presence [10] and development [11-13] of proteinuria in individuals without kidney disease. Furthermore, in numerous large populationbased studies, higher BMI appears associated with the presence [10,14] and development of low estimated GFR, [11,12,15] with more rapid loss of estimated GFR over time, [16] and with the incidence of ESRD [17-20]. Elevated BMI levels, class II obesity and above, have been associated with more rapid progression of CKD in patients with pre-existing CKD [21]. A few studies examining the association of abdominal obesity using WHR or WC with CKD, describe an association between higher girth and albuminuria [22], decreased GFR [10] or incident ESRD [23] independent of BMI level.

Table 1: Studies examining the association of obesity with various measures of CKD.





  

    
Study 

    
Patients 

    
Exposure 

    
Outcomes 

    
Results 

    
Comments 

  

  

    
Prevention of Renal and Vascular End-Stage Disease    (PREVEND) Study [10] 

    
7,676 Dutch individuals without diabetes 

    
Elevated BMI (overweight and obese*), and central fat distribution    (waist-hip ratio)

    
-Presence of urine albumin 30-300 mg/24h

      
-Elevated and diminished GFR

      
 

    
-Obese + central fat: higher risk of albuminuria

      
-Obese +/- central fat: higher risk of elevated GFR

      
-Central fat +/- obesity associated with diminished filtration

    
Cross sectional analysis

  

  

    
Multinational study of hypertensive outpatients [22]

    
20,828 patients from 26 countries

    
BMI and waist circumference

    
Prevalence of albuminuria by dip stick

    
Higher waist circumference associated with albuminuria independent of    BMI

    
Cross sectional analysis

  

  

    
Framingham Multi-Detector Computed Tomography (MDCT) cohort [24] 

    
3,099 individuals

    
Visceral adipose tissue (VAT) and subcutaneous adipose tissue (SAT)

    
Prevalence of UACR >25 mg/g in women and >17 mg/g in men

    
VAT associated with albuminuria in men, but not in women

    
Cross sectional analysis

  

  

    
CARDIA (Coronary Artery Risk Development in Young Adults) study [13]

    
2,354 community-dwelling individuals with normal kidney function aged    28-40 years

    
-Obesity (BMI >30 kg/m2)

      
-Diet and lifestyle-related factors

    
Incident microalbuminuria

    
Obesity (OR 1.9) and unhealthy diet (OR 2.0) associated with incident    albuminuria

    
Low number of events

  

  

    
Hypertension Detection and Follow-Up Program [12]

    
5,897 hypertensive adults

    
Overweight and obese BMI* vs. normal    BMI

    
Incident CKD (1+ or greater proteinuria on urinalysis and/or an eGFR    <60 mL/min/1.73 m2)

    
Both overweight (OR 1.21) and obesity (OR 1.40) associated with    incident CKD

    
Results unchanged after excluding diabetics

  

  

    
Framingham Offspring Study [11]

    
2,676 individuals free of CKD stage 3

    
High vs. normal BMI*

    
-Incident CKD stage 3

      
-Incident proteinuria

    
-Higher BMI not associated with CKD3 after adjustments

      
-Higher BMI associated with increased odds of incident proteinuria

    
Predominantly white, limited geography

  

  

    
Physicians' Health Study [15]

    
11,104 initially healthy men in US

    
-BMI quintiles

      
-Increase in BMI over time (vs. stable    BMI)

    
Incident eGFR <60 mL/min/1.73 m2

    
-Higher baseline BMI and increase in BMI over time both associated    with higher risk of incident CKD

    
Exclusively men

  

  

    
Nation-wide US Veterans Administration cohort [16]

    
3,376,187 US veterans with baseline eGFR =60 mL/min/1.73 m2

    
BMI categories from <20 to >50 kg/m2

    
Rapid decline in kidney function (negative eGFR slope of >5    mL/min/1.73 m2)

    
BMI >30 kg/m2 associated with rapid loss of kidney    function

    
Associations more accentuated in older individuals

  

  

    
Nation-wide population-based study from Sweden [14]

    
926 Swedes with moderate/advanced CKD compared to 998    controls 

    
BMI =25 vs. <25 kg/m2

      
 

    
CKD vs. no CKD

    
Higher BMI associated with 3x higher risk of CKD

    
-Risk strongest in diabetics, but also significantly higher in    non-diabetics

      
-Cross sectional analysis

  

  

    
Nation-wide population based study in Israel [19]

    
1,194,704 adolescent males and females examined for military service 

    
Elevated BMI (overweight and obesity) vs. normal BMI*

    
Incident ESRD

    
Overweight (HR 3.0) and obesity (HR 6.89) associated with higher risk    of ESRD

    
Associations strongest for diabetic ESRD, but also significantly    higher for non-diabetic ESRD

  

  

    
The Nord-Trøndelag Health Study (HUNT-1) [17]

    
74,986 Norwegian adults 

    
BMI categories*

    
Incidence of ESRD or renal death

    
BMI >30 kg/m2 associated with worse outcomes

    
Associations not present in individuals with BL <120/80 mmHg

  

  

    
Community-based screening in Okinawa, Japan [18]

    
100,753 individuals >20 years old

    
BMI quartiles

    
Incidence of ESRD

    
Higher BMI associated with increased risk of ESRD in men, but not in    women

    
Average BMI lower in Japan compared to Western countries

  

  

    
Nation-wide US Veterans Administration cohort [21]

    
453,946 US veterans with baseline eGFR<60 ml/min per 1.73 m2

    
BMI categories from <20 to >50 kg/m2

    
-Incidence of ESRD

      
-Doubling of serum creatinine

      
-Slopes of eGFR

    
Moderate and severe obesity associated with worse renal outcomes

    
Associations present but weaker in patients with more advanced CKD

  

  

    
Kaiser Permanente Northern California [20]

    
320,252 adults with and without baseline CKD

    
Overweight, class I, II and extreme obesity; vs. normal BMI*

    
Incidence of ESRD

    
Linearly higher risk of ESRD with higher BMI categories

    
Associations remained present after adjustment for DM, hypertension    and baseline CKD

  

  

    
REGARDS (Reasons for Geographic and Racial Differences in Stroke)    Study [23]

    
30,239 individuals

    
Elevated waist circumference or BMI

    
Incidence of ESRD

    
BMI above normal not associated with ESRD after adjustment for waist    circumference

      
-Higher waist circumference associated with ESRD

    
Association of waist circumference with ESRD became on-significant    after adjustment for comorbidities and baseline eGFR and proteinuria

  

  

    
*Normal weight:    BMI 18.5 to 24.9 kg/m2; Overweight: BMI 25.0 to 29.9 kg/m2;    Class I obesity: BMI 30.0 to 34.9 kg/m2; Class II obesity: BMI    35.0 to 39.9 kg/m2; Class III obesity: BMI =40 kg/m2

      
BMI: Body Mass    Index; CKD: Chronic Kidney Disease; DM: Diabetes Mellitus; eGFR: estimated    Glomerular Filtration Rate; ESRD: End Stage Renal Disease; HR: Hazard Ratio;    OR: Odds Ratio; UACR: Urine Albumin-Creatinine Ratio

      
 

  










Table 1: Studies examining the association of obesity with various measures of CKD.

Higher visceral adipose tissue measured by computed tomography has been associated with a higher prevalence of albuminuria in men [24]. The observation of a BMI-independent association between abdominal obesity and poorer renal outcomes is also described in relationship with mortality in patients with ESRD [8] and kidney transplant [9], and suggests a direct role of visceral adiposity. In general, the associations between obesity and poorer renal outcomes persist even after adjustments for possible mediators of obesity’s cardiovascular and metabolic effects, such as high blood pressure and diabetes mellitus, suggesting that obesity may affect kidney function through mechanisms in part unrelated to these complications (vide infra).

The deleterious effect of obesity on the kidneys extends to other complications such as nephrolithiasis and kidney malignancies. Higher BMI is associated with an increased prevalence [25] and incidence [26,27] of nephrolithiasis. Furthermore, weight gain over time, and higher baseline WC were also associated with higher incidence of nephrolithiasis [27]. Obesity is associated with various types of malignancies, particularly cancers of the kidneys. In a population-based study of 5.24 million individuals from the UK, a 5 kg/m2 higher BMI was associated with a 25% higher risk of kidney cancers, with 10% of all kidney cancers attributable to excess weight [28]. Another large analysis examining the global burden of obesity on malignancies estimated that 17% and 26% of all kidney cancers in men and women, respectively, were attributable to excess weight [29]. The association between obesity and kidney cancers was consistent in both men and women, and across populations from different parts of the world in a meta-analysis that included data from 221 studies (of which 17 examined kidney cancers) [30]. Among the cancers examined in this meta-analysis, kidney cancers had the third highest risk associated with obesity (relative risk per 5 kg/m2 higher BMI: 1.24, 95%CI 1.20-1.28, p<0.0001) [30].

Mechanisms of action underlying the renal effects of obesity

Obesity results in complex metabolic abnormalities which have wide-ranging effects on diseases affecting the kidneys. The exact mechanisms whereby obesity may worsen or cause CKD remain unclear. The fact that most obese individuals never develop CKD, and the distinction of up to as many as 25% of obese individuals as “metabolically healthy” suggests that increased weight alone is not sufficient to induce kidney damage [31]. Some of the deleterious renal consequences of obesity may be mediated by downstream comorbid conditions such as diabetes mellitus or hypertension, but there are also effects of adiposity which could impact the kidneys directly, induced by the endocrine activity of the adipose tissue via production of (among others) adiponectin [32], leptin [33] and resist in [34] (Figure 1). These include the development of inflammation [35], oxidative stress [36], abnormal lipid metabolism [37], activation of the renin-angiotensin-aldosterone system [38], and increased production of insulin and insulin resistance [39,40].

Figure 1: Putative mechanisms of action whereby obesity causes chronic kidney disease.

    

    
    

    

    Figure 1:  Putative mechanisms of action whereby obesity causes chronic
kidney disease.

These various effects result in specific pathologic changes in the kidneys [41] which could underlie the higher risk of CKD seen in observational studies. These include ectopic lipid accumulation [42] and increased deposition of renal sinus fat [43,44], the development of glomerular hypertension and increased glomerular permeability caused by hyperfiltration-related glomerular filtration barrier injury [45], and ultimately the development of glomerulomegaly [46], and focal or segmental glomerulosclerosis [41] (Figure 2). The incidence of the so-called obesity-related glomerulopathy (ORG) has increased ten-fold between 1986 and 2000 [41]. Importantly, ORG often presents along with pathophysiologic processes related to other conditions or advanced age, conspiring to result in more accentuated kidney damage in patients with high blood pressure [47] or in the elderly [16,39].

Figure 2: Obesity-related perihilar focal segmental glomerulosclerosis on a background of glomerulomegaly. Periodic Acid-Schiff stain, original magnification 400x.

    

    
    

    

    Figure 2:  Obesity-related perihilar focal segmental glomerulosclerosis
on a background of glomerulomegaly. Periodic Acid-Schiff stain, original
magnification 400x.

Obesity is associated with a number of risk factors contributing to the higher incidence and prevalence of nephrolithiasis. Higher body weight is associated with lower urine pH [48] and increased urinary oxalate [49], uric acid, sodium and phosphate excretion [50]. Diets richer in protein and sodium may lead to a more acidic urine and decrease in urinary citrate, also contributing to kidney stone risk. The insulin resistance characteristic of obesity may also predispose to nephrolithiasis [51] through its impact on tubular Na-H exchanger [52] and ammoniagenesis [53], and the promotion of an acidic milieu [54]. Complicating the picture is the fact that some weight loss therapies result in a worsening, rather than an improvement in the risk for kidney stone formation; e.g. gastric surgery can lead to a substantial increase in enteral oxalate absorption and enhanced risk of nephrolithiasis [55].

The mechanisms behind the increased risk of kidney cancers observed in obese individuals are less well characterized. Insulin resistance, and the consequent chronic hyperinsulinemia and increased production of insulin-like growth factor 1 and numerous complex secondary humoral effects may exert stimulating effects on the growth of various types of tumor cells [56]. More recently, the endocrine functions of adipose tissue [57], its effects on immunity [58], and the generation of an inflammatory milieu with complex effects on cancers [59,60] have emerged as additional explanations.

Obesity in patients with advanced kidney disease: The need for a nuanced approach

Considering the above evidence about the overwhelmingly deleterious effects of obesity on various disease processes, it is seemingly counterintuitive that obesity has been consistently associated with lower mortality rates in patients with advanced CKD [21,61] and ESRD [62,63]. Similar “paradoxical” associations have also been described in other populations, such as in patients with congestive heart failure [64], chronic obstructive pulmonary disease [65], rheumatoid arthritis [66], and even in old individuals [67]. It is possible that the seemingly protective effect of a high BMI is the result of the imperfection of BMI as a measure of obesity, as it does not differentiate the effects of adiposity from those of higher non-adipose tissue. Indeed, studies that separated the effects of a higher waist circumference from those of higher BMI showed a reversal of the inverse association with mortality [8,9]. Higher muscle mass has also been shown to explain at least some of the positive effects attributed to elevated BMI [63,68]. However, there is also evidence to suggest that higher adiposity, especially subcutaneous (non-visceral) fat, may also be associated with better outcomes in ESRD patients [62]. Such benefits may indeed be present in patients who have very low short term life expectancy, such as most ESRD patients [69]. Indeed, some studies that examined the association of BMI with time-dependent survival in ESRD have shown a marked contrast between protective short term effects vs. deleterious longer term effects of higher BMI [70]. There are several putative short term benefits that higher body mass could portend, especially to sicker individuals. These include a benefit from the better nutritional status typically seen in obese individuals, and which provides better protein and energy reserves in the face of acute illness, and a higher muscle mass with enhanced antioxidant capacity [63] and lower circulating actin and higher plasma gelsolin levels [71], which are associated with better outcomes. Other hypothetically beneficial characteristics of obesity include a more stable hemodynamic status with mitigation of stress responses and heightened sympathetic and renin-angiotensin activity [72]; increased production of adiponectines [73] and soluble tumor necrosis factor alfa receptors [74] by adipose tissue neutralizing the adverse effects of tumor necrosis factor alfa; enhanced binding of circulating endotoxins [75] by the characteristically higher cholesterol levels seen in obesity; and sequestration of uremic toxins by adipose tissue [76].

Potential interventions for management of obesity

Obesity engenders kidney injury via direct mechanisms through deranged synthesis of various adipose tissue cytokines with nephrotoxic potential, as well as indirectly by triggering diabetes and hypertension, i.e., two conditions that rank among the strongest risk factors for CKD. Perhaps due to the survival advantage of obesity in CKD, the prevalence of end stage kidney disease is on the rise both in the USA [77] and in Europe [78]. Strategies for controlling the obesity related CKD epidemic at population level and for countering the evolution of CKD toward kidney failure in obese patients represent the most tantalizing task that today’s health planners, health managers and nephrologists face.

Countering CKD at population level: Calls for public health interventions in the community to prevent and treat CKD at an early stage have been made by major renal associations, including the International Society of Nephrology (ISN), International Federation of the Kidney Foundation (IFKF), the European renal association (ERA-EDTA) and various national societies. In the USA, Healthy People 2020, a program that sets 10-year health targets for health promotion and prevention goals, focuses both on CKD and obesity. Surveys to detect obese patients, particularly those with a high risk of CKD (e.g. hypertensive and/or diabetic obese people) and those receiving suboptimal care to inform these patients of the potential risk for CKD they are exposed to, is the first step towards developing public health interventions. Acquiring evidence that current interventions to reduce CKD risk in the obese are efficacious and deployable, is an urgent priority to set goals and means for risk modification. Appropriate documentation of existing knowledge distilling the risk and the benefits of primary and secondary prevention interventions in obese people, and new trials in this population to fill knowledge gaps (see below) are needed. Finally, surveillance programs that monitor progress on the detection of at-risk individuals and the effectiveness of prevention programs being deployed [79] constitute the third, fundamental element for establishing efficacious CKD prevention plans at population level.

A successful surveillance system for CKD has already been implemented in some places such as the United Kingdom (UK) [80]. A campaign to disseminate and apply K-DOQI CKD guidelines in primary care within the UK National Health Service was launched. This progressively increased the adoption of K-DOQI guidelines and, also thanks to specific incentives for UK general physicians to detect CKD, led to an impressive improvement in the detection and care of CKD, i.e. better control of hypertension and increased use of angiotensin-converting enzyme and angiotensin receptor blockers [80]. This system may serve as a platform to improve the prevention of obesity-related CKD. Campaigns aiming at reducing the obesity burden are now at center stage worldwide and are strongly recommended by the WHO and it is expected that these campaigns will reduce the incidence of obesity-related complications, including CKD. However obesity-related goals in obese CKD patients remain vaguely formulated, largely because of the paucity of high-level evidence intervention studies to modify obesity in CKD patients [81].

Prevention of CKD progression in obese people with CKD: Observational studies in metabolically healthy obese subjects show that the obese phenotype unassociated with metabolic abnormalities per se predicts a higher risk for incident CKD [82] suggesting that obesity per se may engender renal dysfunction and kidney damage even without diabetes or hypertension (vide supra). In overweight or obese diabetic patients, a lifestyle intervention including caloric restriction and increased physical activity compared with a standard follow up based on education and support to sustain diabetes treatment reduced the risk for incident CKD by 30%, although it did not affect the incidence of cardiovascular events [83]. Such a protective effect was partly due to reductions in body weight, HbA1c, and systolic BP. No safety concerns regarding kidney-related adverse events were seen [83]. In a recent meta-analysis collating experimental studies in obese CKD patients, interventions aimed at reducing body weight showed coherent reductions in blood pressure, glomerular hyper-filtration and proteinuria [81]. A thorough post-hoc analysis of the REIN study showed that the nephron-protective effect of ACE inhibition in proteinuric CKD patients was maximal in obese CKD patients, but minimal in CKD patients with normal or low BMI [84]. Of note, bariatric surgical intervention have been suggested for selected CKD and ESRD patients including dialysis patients who are waitlisted for kidney transplantation [85-87].

Globally, these experimental findings provide a proof of concept for the usefulness of weight reduction and ACE inhibition interventions in the treatment of CKD in the obese. Studies showing a survival benefit of increased BMI in CKD patients, however, remain to be explained [88]. These findings limit our ability to make strong recommendations about the usefulness and the safety of weight reduction among individuals with more advanced stages of CKD. Lifestyle recommendations to reduce body weight in obese people at risk for CKD and in those with early CKD appear justified, particularly recommendations for the control of diabetes and hypertension. As the independent effect of obesity control on the incidence and progression of CKD is difficult to disentangle from the effects of hypertension and type 2 diabetes, recommendation of weight loss in the minority of metabolically healthy, non-hypertensive obese patients remains unwarranted. These considerations suggest that a therapeutic approach to overweight and obesity in patients with advanced CKD or other significant comorbid conditions has to be pursued carefully, with proper considerations of the expected benefits and potential complications of weight loss over the life span of the individual patient.

Conclusion

The worldwide epidemic of obesity affects the Earth’s population in many ways. Diseases of the kidneys, including CKD, nephrolithiasis and kidney cancers are among the more insidious effects of obesity, but which nonetheless have wide ranging deleterious consequences, ultimately leading to significant excess morbidity and mortality and excess costs to individuals and the entire society. Populationwide interventions to control obesity could have beneficial effects in preventing the development, or delaying the progression of CKD. It is incumbent upon the entire healthcare community to devise long-ranging strategies towards improving the understanding of the links between obesity and kidney diseases, and to determine optimal strategies to stem the tide. The 2017 World Kidney Day is an important opportunity to increase education and awareness to that end.

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Citation: Kovesdy CP, Furth S and Zoccali C. Obesity and Kidney Disease: Hidden Consequences of the Epidemic. Austin J Nephrol Hypertens. 2016; 3(2): 1062. ISSN:2381-8964