How to resolve confusion in the clinical setting for the diagnosis of heterozygous COL4A3 or COL4A4 gene variants? Discussion and suggestions from nephrologists

TBMN is a common hereditary nephritis which affects at least 1% of the population [2]. In the 1960s, several families with isolated hematuria were reported as benign familial hematuria (BFH) [18]. In 1973, thinning of the GBM by electron microscopy (EM) was observed in BFH families [19]. Whilst the authors stated that this condition could be labeled “benign” only after prolonged observation, the term “TBMN” has often been used synonymously with “BFH” until recently.

After the 1980s, some researchers reported that cases of TBMN were occasionally accompanied by severe proteinuria [20] or development of ESRD [21]. However, it was thought that proteinuria or renal dysfunction may be due to other coincidental factors such as glomerulonephritis or hypertension, rather than TBMN itself.

In 1994, Mochizuki et al. revealed that homozygous or compound heterozygous mutations in COL4A3 or COL4A4 cause autosomal recessive AS (ARAS) [22]. Following on from this, Lemmek et al. linked heterozygous COL4A4 mutation to TBMN patients [8]. Subsequently, several groups confirmed that at least 40% of TBMN was caused by heterozygous COL4A3 or COL4A4 mutations [2]. Consequently, some researchers stated that “TBMN/BFH can represent a carrier status of ARAS” [8].

In the late 2000s, researchers from Cyprus showed that 14–35% of TBMN patients with a heterozygous COL4A3 or COL4A4 gene mutation developed ESRD later in life, accompanied by pathological findings of FSGS [3, 4, 23]. Therefore, they concluded that renal prognosis of TBMN is not necessarily benign and that the term “BFH” is a misnomer.

AS is a hereditary nephritis caused by the mutation of COL4A3/A4/A5 genes which encode α3/α4/α5 chains of type IV collagen. Approximately 80% of AS is X-linked AS (XLAS) and typical male XLAS patients present with hearing loss, hematuria and proteinuria in childhood, which progresses to ESRD in the 2nd to 3rd decade of life [1]. ARAS accounts for 15% and presents with similar clinical phenotypes to male XLAS, with equal frequency and severity in males and females [24]. In contrast, ADAS accounts for < 5% and its disease concept has been unclear until recently.

In 1927, Alport AC reported a family of hereditary nephropathy accompanied by deafness, which was named AS after his death in 1961 [25]. Whilst the mode of inheritance was thought to be predominantly X-linked, as males were more severely affected, some researchers argued an autosomal dominant inheritance mode, as there was a transmission from affected father to son [26]. In late 1960s, characteristic changes in the GBM using EM was observed [27]. Subsequently, Flinter et al. described a diagnostic criteria based on clinical symptoms and the appearance of GBM in 1988 [28], aiming to facilitate the identification of classical AS, namely, XLAS.

In 1990, a mutation in COL4A5 was detected in families with XLAS [29] and subsequently a mutation in COL4A3 or COL4A4 was detected in families with ARAS [22]. At that time, typical pattern of lack of α5 chains of type IV collagen [α5 (IV)] by immunohistochemical (IHC) analysis was reported in patients with XLAS and ARAS [30, 31]. Some researchers also reported positive staining for α5 (IV) in patients with autosomal dominant inheritance mode [32].

In 1997, Jefferson et al. provided the first evidence of ADAS, identifying heterozygous mutation in COL4A3 in a family from Northern Ireland [5]. Out of seven patients, one male patient developed ESRD at 35 years accompanied by deafness. Kidney biopsies from four patients showed irregular thickening of GBM. At that time, as described above, Lemmik. et al. reported that heterozygous mutation in COL4A3 or COL4A4 also causes TBMN/BFH and that the same gene mutation either homozygosis or compound heterozygosis can cause ARAS [8]. Therefore, they stated that these gene mutations show various spectra ranging from TBMN/BFH, ARAS, and ADAS [5, 8], leading to the proposal of the concept of “Type IV collagen-related nephropathy”.

After the first report by Jefferson et al., other families with ADAS were reported mostly from Europe [9, 33, 34]. However, since not all patients underwent kidney biopsy and most patients did not have extrarenal manifestations, some experts questioned if all these patients should have been diagnosed with ADAS. In 2016, Kamiyoshi et al. reported genetic, clinical, and pathologic backgrounds of ADAS, using the largest cohort of 72 patients from 16 families [6]. The median age at detection of proteinuria was 17 years and 13% developed ESRD at the median age of 70 years. Hearing loss and ocular abnormalities were reported in 4% of the patients. Light microscopy of kidney biopsies showed non-specific lesions including minor glomerular abnormality, mesangial proliferation, and FSGS. IHC analysis of α5(IV) showed normal expression in all patients. EM analysis showed 44% of the patients with thinning, but without lamellation of the GBM. Therefore, they concluded that it is difficult to make a definitive diagnosis of ADAS based on clinicopathological findings and genetic analysis is essential for an accurate diagnosis. Furthermore, even within one family, clinical severity differed significantly and some individuals developed ESRD, whereas others showed no urinary abnormality. No genotype–phenotype correlations were observed, and no modifier genes were identified among the known podocyte-related genes. These results established the concept of ADAS, and also revealed that both “TBMN developing ESRD” and “ADAS” are caused by COL4A3 or COL4A4 heterozygous mutations.

Due to the increased availability of NGS, the number of reports of ADAS is rapidly increasing [9, 10, 34]. For example, Yamamura et al. performed genetic analysis for 390 families with suspicion of AS and showed that XLAS represented 74% of the cases, ARAS 9%, and ADAS 17%, which was notably higher than previously reported [10]. However, some experts still question the diagnosis of ADAS [14].

The diagnosis of patients with heterozygous mutations in COL4A3 or COL4A4 is controversial [7, 13‐17, 35], resulting in confusion among nephrologists. This is primarily because the phenotype of heterozygous COL4A3 or COL4A4 variants varies from no urinary abnormality, to isolated hematuria, to ESRD. In addition, these patients are given various diagnostic terms based on clinical, pathological, genetic, and etiological features (Fig. 1). Besides the diagnostic terms “TBMN”, “BFH”, and “ADAS” described previously, some patients are classified as “dual diagnosis of FSGS and TBMN” or are even mistaken as “familial FSGS”, when FSGS is pathologically proven [36]. Also, some researchers use the term “Autosomal dominant later-onset Alport-related nephropathy” [35], or “Autosomal dominant collagen IV-related nephropathy” [37]. As the report of patients with heterozygous COL4A3 or COL4A4 variants rapidly increases, there are ongoing discussions between the experts regarding the diagnosis of this condition [7, 13‐17, 35].

Currently, many researchers believe that the term “TBMN” is not appropriate to describe this condition. This is because “TBMN” is a purely pathological description and implies good clinical outcomes because the term “TBMN” has been used synonymously with “BFH” for a long period. However, renal prognosis for these cases is unpredictable, unless clinicopathological features are observed for a long period. It must also be noted that pathological TBMN can be found in young patients with AS in any inheritance mode [6, 38]. Therefore, some experts insist that diagnosis of TBMN may underestimate the risk of ESRD and deprive these patients of the early treatment.

The diagnostic term ADAS is controversial. Some experts do not accept using the term ADAS [13‐15]. This is because most individuals with heterozygous COL4A3 or COL4A4 mutations show only hematuria with GBM thinning without progressive renal dysfunction and deafness, nor ocular abnormalities. Therefore, it is considered that these individuals do not fulfill the criteria for AS, and they believe that diagnosis of ADAS will increase anxiety in individuals who actually have low risks of ESRD. Furthermore, the term autosomal dominant implies that half of the affected individuals’ offspring develop AS and ESRD; however, this is not true in heterozygous cases. Actually, even between individuals in a family with the same variants, some family members develop ESRD while some are carriers without any urinary abnormalities. Therefore, they insist that kidney dysfunction might be explained by secondary factors such as modifier genes, coincidental other renal diseases, or other acquired factors including hypertension, diabetes, and obesity [2, 14, 23, 35]. However, to date, how these factors influence patients with ADAS remains largely unknown. Furthermore, they also stated that ADAS should not be used for the carrier status of ARAS because it is not consistent with the practice for other hereditary diseases. For example, in cases with polycystic kidney disease (PKD), ADPKD is caused by the mutations in PKD1 or PKD2 genes, whereas ARPKD is caused by mutations in PKHD1 gene. Thus, ADPKD and ARPKD are independent diseases. On the other hand, ADAS and ARAS are caused by mutations in the same genes and they are not completely independent diseases. In other words, when both parents have heterozygous COL4A3 or COL4A4 variants, some of their children can develop ARAS and there can be both patients with ADAS and ARAS in the same families. These relationships between ADAS and ARAS are different from other genetic diseases including PKD. In general, carrier status of “autosomal recessive” diseases are not diagnosed as “autosomal dominant” diseases. Therefore, some experts insist that diagnostic term ADAS will cause confusion in clinical settings. Although they recognize that TBMN is not a satisfactory term, they continue to use this term as it is already commonly accepted worldwide [14, 15].

In contrast, many experts recommend the use of the term ADAS in patients with at least hematuria. Since this condition is caused by heterozygous mutations in COL4A3 or COL4A4 and is transmitted in an autosomal dominant fashion, these experts believe that these patients should be diagnosed with ADAS. Although it progresses slower compared to XLAS or ARAS, some patients with ADAS still develop ESRD. Consequently, they insist that diagnosis of ADAS will increase the number of patients who will receive appropriate monitoring and treatment. Of note, some experts have recently proposed a new classification for AS and have stated that individuals with heterozygous mutations in COL4A3 or COL4A4 should be classified as ADAS, including patients previously diagnosed as TBMN/BFH [17]. Adding to the confusion among nephrologists, however, is that other experts insist that it is preferable to wait for a full understanding of the factors determining renal prognosis before changing terminology [14, 15].

For most nephrologists, especially in adult section who are not currently familiar with this condition, it is difficult to accept the current complicated situation regarding the diagnosis of this condition. For example, there are some patients who are diagnosed as TBMN at a young age; however, this diagnosis is replaced by ADAS after kidney dysfunction becomes evident later in life. In such cases, it is difficult to determine when patients are TBMN and from when they are ADAS. Therefore, we are very hopeful that there soon will be a consensus with a simple and easy-to-follow classification. From nephrologists’ perspective, we believe that diagnostic term ADAS is significant as most nephrologists still have a strong fixed idea that “TBMN is benign”, misleading our clinical practice. On the other hand, diagnosis of ADAS allows us to follow up these patients carefully. Therefore, we suggest that the common term “ADAS” is used for all cases with heterozygous mutation for COL4A3 or COL4A4 with urine abnormality.

It is important for nephrologists to recognize this disease and current confusion in diagnosis. We recently reported that 69% of cases with adult nephritis accompanied by GBM thinning or thickening who were unable to receive accurate diagnosis clinicopathologically were diagnosed as ADAS by genetic analysis [12]. Furthermore, in a recent paper with a large cohort, COL4A3 or COL4A4 gene variants contributed to 16% of 312 cases with CKD [11]. These findings indicate the existence of many undiagnosed patients with ADAS. This is because diagnosis of ADAS is difficult as they lack typical features for AS. Therefore, it is important for nephrologists to recognize this condition and perform genetic analysis for appropriate patients.

Although the indication of genetic analysis is different between countries, NGS before invasive tissue biopsy is already available in several countries. However, genetic testing is still generally not performed when patients and family members present with only hematuria. This is because genetic tests for cases with isolated hematuria can increase anxiety in individuals who actually have low risk of ESRD and also increase medical costs. Therefore, indication of genetic tests should be considered carefully. Currently, genetic analysis is recommended when patients have hematuria with a family history of kidney dysfunction, or when patients have mild to moderate proteinuria or kidney dysfunction, with a family history of hematuria. In sporadic cases, genetic analysis is recommended when kidney biopsy showed GBM thinning and/or lamellation. It is true, however, that it is still common to perform kidney biopsy prior to genetic analysis in patients suspected of having ADAS, due to a lack of recognition of this condition. In fact, there are many patients with AS who are misdiagnosed with FSGS, non-immunoglobulin A (IgA) mesangial proliferative glomerulonephritis, or even familial IgA nephropathy [36, 39], resulting in unnecessary kidney biopsies or immunosuppressive therapies. Therefore, it is important to consider genetic analysis in patients with glomerulonephritis accompanied by GBM thinning and/or lamellation, or even in patients diagnosed with FSGS or IgA nephropathy but are resistant to conventional treatments or with a familial history of hematuria or ESRD. It should also be noted that conditions regarding genetic test for AS are different between countries. For example, it is covered by health insurance in Australia. In the US, sponsored, no-charge genetic testing is performed. On the other hand, it is conducted under laboratory study levels in Japan, Korea, Germany, and many other countries. Therefore, there is still a need to improve genetic testing systems to be widely used as a diagnostic tool to make accurate diagnosis of these cases.

Diagnosis of ADAS is significant because it facilitates careful follow-up and early treatment. Recent large retrospective studies reported that the treatment with angiotensin-converting enzyme inhibitors (ACEIs) delayed the progression into ESRD, even in cases of male XLAS or ARAS (40). Consequently, it is expected that treatment with ACEIs will be even more effective in delaying the progression of ESRD in ADAS patients, who have milder phenotypes compared to male XLAS or ARAS. Therefore, individuals and their family members with heterozygous COL4A3 or COL4A4 gene variants, even when they have only isolated hematuria, require annual monitoring of blood pressure, urine protein excretion, and renal function. When proteinuria or hypertension is detected, treatment with renin–angiotensin system inhibitors should commence immediately [13, 17]. It is also true that health checkup system is different between countries. However, even in countries where annual checkup is not easily available, it is recommended to follow these patients at least once per year, if possible. We also have to note that some new medicines have initiated clinical trials, such as bardoxolone methyl (Phase II/III) and RG-012 (effect on microRNA-21 interference, Phase II) [7, 16]. These novel therapies for AS, including ADAS, might change future treatment options.