Minimizing Risk of Nephrogenic systemic fibrosis in Cardiovascular Magnetic Resonance

Gadolinium is one of the 14 elements of the lanthanide group. Virtually all of its compounds contain it as the paramagnetic Gd³⁺ ion which has seven unpaired electrons in its half-filled 4 f outer shell. Gd³⁺ has a long electronic relaxation time based on its totally symmetric S state making it well suited for use as an MR contrast agent. It accelerates the relaxation of the water molecules present in the tissue, giving rise to an enhanced signal on T1-weighted images and, together with appropriate sequence parameters, an improved image contrast. However, gadolinium, like most metals, interferes with the complex biochemical processes of living organisms. In particular, it can act as a competitive inhibitor of calcium ions due to its large ionic radius (0.97 Å vs. 1.06 Å for Ca²⁺) and its high ionic charge. As a result various physiological processes involving Ca²⁺ can be influenced by the presence of Gd³⁺ such as Ca²⁺-activated ATPase in the sarcoplasmatic reticulum of skeletal muscle fibres, the reticuloendothelial system and some other enzymes such as dehydrogenases and glutathione S transferases. It is also known that Gd³⁺ has an inhibitory effect on Kupffer cells [4].

The toxic effects of Gd³⁺ can be suppressed by encasing it in an organic chelator. A variety of such chelators have been FDA/EMEA approved for use in patients and others are still being investigated [12‐14]. The contrast agents in clinical use are based on the linear ionic chelator diethylenetriamine pentaacetic acid (often dubbed as DTPA or "pentetic acid"), the linear non-ionic chelator benzyloxyproprionictetra- acetate (“BOPTA”) or on the cyclic ionic chelator tetraazacyclododecane tetraacetic acid (DOTA). Other cyclic non-ionic chelators are tetraazacycl ododecane (DO3A). Stability of these agents is characterized in two ways: Thermodynamic stability describes the tendency of the chelate to dissociate into its components given an unlimited amount of time. It is expressed numerically as the logarithm of the stability constant. Kinetic stability describes the timescale of the dissociation expressed either as a rate constant or a half-life. Both characteristics depend on the surrounding milieu: Decreasing pH and increasing temperature favour dissociation [15]. As a rule, the macrocyclic chelates are several orders of magnitude more stable with regard to dissociation and transmetalation than their linear counterparts [16‐18]. Furthermore, the presence of ions such as Ca²⁺, Cu²⁺ or Zn²⁺ which can replace Gd³⁺ from the chelate in a transmetalation reaction promote the unwanted release of Gd³⁺ exposing tissues to its toxic effects [19]. Indeed, early in vivo studies using radioisotope labelled Gd chelates indicate a relationship between kinetic stability and tissue-uptake of gadolinium [20].

Besides the characterization in terms of macrocyclic and linear chelate structures, the nine currently available GBCAs (Table 1, Figure 1) can also be categorized by ionicity. Non-ionic Gd³⁺ chelates cause less osmotic stress because they do not require counterions such as Na⁺ in their formulations. They are closer to ionic neutrality with lower viscosity, and are less hydrophilic than ionic Gd³⁺ chelates [21]. As with iodinated contrast, non-ionic Gd³⁺ chelates appear to have a lower rate of allergic reactions [22]. Unfortunately non-ionic linear chelates are also less stable than their negatively charged analogs. With the exception of three linear ionic GBCAs that have lipophilic groups in their chelate structures (Gadobenate, Gadoxetate, Gadofosvescet), GBCAs are eliminated exclusively via the renal pathway. The estimated half-life of renal elimination of GBCAs for patients with normal renal function is about 90 min. However, with decreasing renal function the effective half-life increases to up to 18 – 34 hours [16, 23]. Within this timescale gadolinium release for the linear chelates may be significant [20].

Two of the three mentioned linear, ionic GBCAs (Gadobenate, Gadoxetate) have an aromatic component within the chelate structure that allows hepatocellular uptake and partial excretion via the biliary pathway. The third mentioned GBCA (Gadofosveset) has a biphenylcyclohexyl group that reversibly binds to albumin, extending the plasma half-life to about 18.5 hours for patients with a normal renal function [16, 19].

NSF occurs in patients with acute or chronic renal failure [32, 33]. The vast majority of NSF cases (approximately 95 %) have occurred in renal failure patients who received GBCA enhanced CMR imaging techniques prior to symptom onset [34]. Thus, it is likely that GBCAs play a role in triggering NSF. All GBCA stimulate the proliferation of fibroblasts, the linear GBCAs show a more potent stimulation than macrocyclic GBCAs [35‐38] which raises the possibility that GBCA dissociation from the chelator is not necessary for NSF to occur. One hypothesis is that macrophages phagocytose the Gd³⁺ complexes that then, being located in intracellular lysosomes, stimulate the production of cytokines, and growth factors [39, 40]. Local inflammation may be due to local Gd³⁺ deposition, that is triggered by local CD68+ or XIIIa+ dendritic cells, and a systemic inflammatory response that is associated with CD34+ fibrocytes that originate from the bone marrow [41]. The heterogeneous phenotypes of cells found in NSF lesion imply that both local and systemic inflammatory mechanisms might coexist [42]. TGF-beta1 levels are elevated in patients with NSF, and some studies have shown increased decortin levels, alpha-smooth muscle actin and hyaluron synthesis [38, 43‐45]. A modulation of collagen syntheses with an increase of Collagen I and III production as well as an increase in fibronectin expression has been documented [38, 46], as well as increased VEGF levels, Ostepontin, and TIMP-1 expression [47]. At least for one of the GBCAs (Gadodiamide), an effect on the expression of chemokine genes has been tracked down as the presence of GBCAs increase the activation of a NFκB pathway. It shows that exposure to GBCAs and the included Gd³⁺ is a potent stimulator of normal macrophages [48]. Most recent studies suggest that possibly other cells might be involved in the development of NSF as well, such as tissue monocytes and macrophages in the peripheral blood [49].

Additionally, it has been discussed that pro-inflammatory events, like vascular thrombosis, myocardial infarction, trauma, sepsis or recent surgery might contribute to the development of NSF [33]. Sepsis might even trigger the onset of NSF without exposure to GBCAs [50]. A resent work showed that the presence of GBCA increases DNA damage in lymphocytes [51]. The presence of high iron and erythropoetin levels are suspected to contribute to the development of NSF as well [44, 52‐54]. The Gd³⁺ complexes seem to have an effect on calcium phosphate as a study showed that the calcium phosphate precipitation is increased thus activating macrophages [55].

Patients with NSF present with skin lesions typically beginning on the distal extremities starting with indurated plaques and papules especially on edematous lower extremities, later on the upper extremities, trunk and eye section develop over days to several weeks and later show a woody texture. The plaques are described as brawny, and the skin may develop hyperpigmentation [56][57]. NSF lesions usually occur symmetrically. Patients may report sharp pain as well as pruritus, causalgias and paresthesias in afflicted areas. Stiffness and joint contractures can lead to decreased mobility. The progression is rapid in an estimated 5 % of cases [8] leading to immobility within weeks and in a few instances death has been attributed to NSF. Besides skin developing lesions, internal organs can be afflicted including lung, heart, liver, bones and kidneys [33, 34].

NSF diagnosis is usually postulated upon the medical history/physical exam and confirmed with a deep punch skin biopsy [2, 56, 58, 59]. Eosin and hematoxylin staining are used for demonstrating the typical features. The skin biopsy shows a dermal fibrosis with a high density of CD 34 positive and procollagen I positive fibrocytes (circulating fibrocytes) and collagen bundles with prominent clefts between the bundles. Besides these collagen bundles elastic fibres can be detected as well. Additionally, but not required for diagnosis of NSF, factor XIIIa positive dendritic cells may be detected [56]. However the histopathological and clinical features can overlap with other entities. Among these are Lipodermatosclerosis, Scleroderma and Morphea, Scleromyxedema, Porphyria cutanea tarda, Spanish toxic Oil syndrome, eosinophilic fasciitis and Eosinophilia- myalgia syndrome and chronic graft versus host disease [2, 58, 60]. It is necessary to combine both the clinical features and the histopathologic findings in order to avoid misdiagnosis.

Exposure to gadolinium might arouse suspicion towards the diagnosis of NSF however it has to be stressed that exposure to GBCAs does not factor into the diagnosis. The lack of GBCA exposures does not exclude NSF as diagnosis, as in about 5 % of NSF patients no GBCA exposure prior to symptom onset could be found.

Besides the development of NSF other more acute reactions to GBCA exposure have been described. Symptoms that imply the development of septicaemia have been described within 12-36 h after administration of GBCA [61]. Allergic reactions albeit rare are another GBCA risk [22][62]. The possibility of deterioration in renal function after GBCA exposure in renal failure patients is controversial but in the usually administered dosages GBCAs are less nephrotoxic than iodinated contrast agents even with the high doses used for MR viability imaging and MR Angiography [63, 64].

The incidence of NSF prior to 2008 varied widely among different institutions ranging from 0.26 % in patients on dialysis without any contributing factors to up to 8.8 % in patients with a eGFR smaller than 15 ml/min/1.73 m³ without hemodialysis [50, 65]. A study published in 2007 in another center calculated an absolute risk for developing NSF in patients on chronic dialysis of 2.4 % per GBCA enhanced study and an absolute risk of 3.4 % per patient [66]. The combination of renal insufficiency and proinflammatory processes (e.g. operations, thrombembolic events, endothelial/vascular injury) adds up to an NSF incidence of 4.6 % [33]. The incidence is further increased when renal failure patients on dialysis develop sepsis, and has been estimated at 6.3 % [50]. It is also noteworthy that the overwhelming majority of cases was either on dialysis or had an eGFR < 15 ml/min/1,73 m³. Only a handful of cases estimated in patients with an estimated GFR > 30 ml/min/1,73 m³and most of these were patients in acute renal failure where GFR estimation is unreliable. The incidence of reported NSF cases in patients with a normal renal function is zero.

The vast majority of NSF cases have been reported in patients who underwent GBCA enhanced imaging however, about 5 % of NSF cases showed no traceable exposure to GBCAs prior to NSF onset [34]. The exposure to GBCAs seems to be a cofactor to developing NSF, with the incidence depending besides the already mentioned patients collective also on the type and dose of GBCA. In patients who received a GBCA dose according to the labeling (e.g. 0.1 mmol/kg) overall incidence is near zero, regardless of their renal function. Based on a report of Prince (2008, [65]) the use of higher GBCA doses such as double or triple dose GBCA administration (0,2 – 0,3 mmol/kg) increases the incidence from zero to 0,17 % for some of the available contrast agents. These were Gadodiamide and Gadobenate, while this effect was not detected with Gadopentetate dimeglumine and Gadoteridol. The incidence rises when GBCAs in high doses are used in patients with renal failure. One of the reports describes the incidence in this setting at 8.0 % [65, 67‐69].

The majority of reported cases are associated with non-ionic linear contrast agents (Gadodiamide or Gadoversetamide). Another agent associated with NSF is Gadopentate dimeglumine, but there are markedly fewer cases with Gadopentate dimeglumine than with Gadodiamide in spite of Gadopentetate dimeglumine having greater market share. Based on data presented at the FDA Joint Meeting of the Cardiovascular and Renal Drugs and Drug Safety Advisory Committee (Dec. 2009, observed time frame 2005–2009), 382 cases of NSF are related to the administration of Gadodiamide (estimated doses 13 million worldwide), 195 cases related to the administration of Gadopentetate dimeglumine (estimated doses 23 million doses worldwide) and 35 cases are attributed to Gadoversetamide (estimated 4.7 million doses worldwide). To date, no cases have been associated with the administration of Gadoxetate or Gadofosveset [70].

The American NSF registry has documented over 355 proven cases of NSF so far, however, other groups have reported deviant numbers, e.g. Zou et al. report of 408 cases that were biopsy confirmed [71]. Most likely, not all cases have been reported to the NSF registry, but directly to the FDA or not at all.

NSF is rarely seen in pediatric patients [72‐74]. The youngest known case of NSF is a 6 year old patient even though many newborn babies with immature kidneys in the past received high doses of GBCA for multiple MR scans to assess congenital heart disease. This suggests that infants and newborns may be a protected population [63].

Many NSF patients have improved or even been cured with restoration of normal renal function. This has occurred when acute renal failure resolves and with renal transplantation. Otherwise, there is no proven effective therapy for the treatment of NSF and to date the treatment options are limited to symptomatic relief. Physical therapy supposedly improves the range of motion [75]. Pain medication usually is needed and includes the use of opioids, NSAR´s, steroids and antidepressants. A single case reports that acetazolamide showed a good pain relieving effect in a meningeal affection of NSF. In some cases intravenous procainamid has been shown to suppress the nociceptive aspects of pain. However, its application has to be performed under continuous cardiac monitoring.

The treatment options for NSF are based on case studies with limited numbers of patients. In the early days of NSF, the benefits of intense hemodialysis were discussed. In patients with end stage kidney disease approximately 98 % of the Gadolinium that freely circulate in the blood is removed with 3 hemodialysis cycles. Not more than 30 % of the Gadolinium chelates are removed with conventional dialysis techniques. Use of ultrapure dialysate and a high bicarbonate concentration combined with high flow for a duration of 5–6 h is said to achieve the best clearance rate [76]. There are some cases where a renal transplant and the resulting improved renal function lead to a decrease in the NSF symptoms. Among other discussed therapy options that were published are the extracorporal photopheresis, plasmapheris, UV-A1 Therapy, high dose intravenous Immunoglobulins, Imatinib Mesylate, Rabamycine and Pentoxifylline. The NSF registry additionally mentions some therapeutic regimens that were anecdotally reported, namely topical Dovonex, Cytoxan and Thalidomide. The use of oral steroids was discussed as well however the reports on the effectiveness were inconsistent (Table 2) [76‐89].

Considering the small numbers of case reports and the fact that NSF can possibly be avoided by preventive measures, the focus of further attention should be primarily on prevention.

The FDA was the first agency to release a public health advisory back in 2006 when the association of GBCA and NSF was not as convincing. However the linkage of high dose GBCA with NSF was suspected, accordingly the advisory stated that only if deemed necessary patients with advanced kidney failure (dialysis or eGFR < 15 ml/min/1.73 m²) should receive imaging studies using GBCA. An update in 2007 extended the patient collective at risk to patients with an eGFR of less than 30 ml/min/1.72 m² and also linked the induction of NSF to the hepato-renal syndrome and liver transplants. A screening of the renal function was proposed. GBCA dose should not exceed the FDA approved levels. In 2010 the latest FDA recommendations explicitly contraindicated Gadodiamide, Gadoversetamide and Gadopentetate dimeglumine use in patients with acute kidney disease or chronic severe kidney disease (eGFR<30). In general all GBCA should be avoided in patients with suspected or known impaired drug elimination unless the diagnostic GBCA based study is necessary. It is again stressed that the recommended dosage must not be exceeded and repeat dosing should be delayed until sufficient time has passed for the first dose to be completely eliminated. This might be less than one day for patients with normal renal function but up to a week for patients for severe chronic renal disease. The screening of the renal function and good documentation are also obligatory (Table 3) [90]. It should be also noted, that only little data on the safety of GBCAs for pediatric patients and almost no data for children younger than 2 years old is available.

The European Medicines Agency (EMA) has defined three risk classes of Gadolinium- based contrast agents. For each of them, the EMA has defined measures to reduce the risk of NSF.

1. High riskGadodiamide; Gadoversetamide, Gadopentetate Dimeglumine

2. Intermediate riskGadobenate Dimeglumine; Gadoxetate Disodium; Gadofosveset

3. Low riskGadobutrol, Gadoteridol; Gadoterate Meglumine

The EMEA’s recommendations on the use of GBCAs are based on this classification (see Table 4). However the concern about newborns is controversial because there are no known cases of NSF in any patient less than 6 years old in spite of a extensive use of high doses of gadolinium based contrast agents for evaluating congenital heart disease in this population [63]. The guidelines also point to the necessity of good documentation of contrast agent type and dose [92] which has not been reliable in the past (Table 4) [93].

The European Society of Urogenital Radiology agrees with the EME on three risk classes for Gadolinium based contrast agents. Additionally, the ESUR defines three risk classes for patients. Patients with chronic kidney disease (CKD) stage 4 and 5 (eGFR < 30 ml/min), patients on dialysis and patients with impaired renal function and pending or received liver transplant are considered high risk patients. Patients with CKD stage 3 and small children younger than 1 year old have a lower risk and with regards to renal function healthy patients are at no risk for developing NSF. The EUSR guidelines also mention the treatment of pregnant women. Due to lack of experience, these patients are to be treated according to the protocol for infants [94].

Further preventative measures should be strived for. It is theorized that low iron serum levels, and an optimized Calcium, phosphate and acid base balance before injection of GBCAs may protect against the development of NSF [85]. Recent research has focused on the goal to limit GBCA doses as far as possible in order to still ensure good image quality. Some authors have reported sufficient image quality in 3 T scanners e.g. for abdominal imaging with 0,025 mmol/kg GBCA at 3 T [95], 0,05 mmol/kg for soft tissue characterization [96] and with 0,05 mmol/kg for vascular malformations [97]. Modifications in CE-MRA protocols offer further reduction of contrast agent doses [98].

The American College of Radiology (ACR) recommendations of 2010 agree with the other guidelines on the associations of GBCA exposure, dosage relations and kidney function. The need for adequately assessing the renal function has been highlighted. In the opinion of the ACR patients at risk, e.g. patients with a past medical history of a renal disease, aged above 60 years old, who have hypertension or diabetes mellitus, should be tested for their renal function 6 weeks prior the planned CMR study. Additionally, a verbal assessment might be helpful. The recommendations for the specific patient groups, divided by their renal function is listed in Table 5[99].

The recommendations of the above mentioned guidelines can be incorporated into an easy to use short work sheet for non- pregnant adults for everyday use (Figure 2, Table 6: list of current label doses).