- Research article
- Open Access
MEN1 redefined, a clinical comparison of mutation-positive and mutation-negative patients
BMC Medicine volume 14, Article number: 182 (2016)
Multiple Endocrine Neoplasia type 1 (MEN1) is diagnosed when two out of the three primary MEN1-associated endocrine tumors occur in a patient. Up to 10–30 % of those patients have no mutation in the MEN1 gene. It is unclear if the phenotype and course of the disease of mutation-negative patients is comparable with mutation-positive patients and if these patients have true MEN1. The present study aims to describe and compare the clinical course of MEN1 mutation-negative patients with two out of the three main MEN1 manifestations and mutation-positive patients during long-term follow-up.
This is a cohort study performed using the Dutch MEN1 database, including > 90 % of the Dutch MEN1 population.
A total of 293 (90.7 %) mutation-positive and 30 (9.3 %) mutation-negative MEN1 patients were included. Median age of developing the first main MEN1 manifestation was higher in mutation-negative patients (46 vs. 33 years) (P = 0.007). Mutation-negative patients did not develop a third main MEN1 manifestation in the course of follow-up compared to 48.3 % of mutation-positive patients (P < 0.001). Median survival in mutation-positive patients was estimated at 73.0 years (95 % CI, 69.5–76.5) compared to 87.0 years (95 % CI not available) in mutation-negative patients (P = 0.001).
Mutation-positive and mutation-negative MEN1 patients have a different phenotype and clinical course. Mutation-negative patients develop MEN1 manifestations at higher age and have a life expectancy comparable with the general population. The apparent differences in clinical course suggest that MEN1 mutation-negative patients do not have true MEN1, but another MEN1-like syndrome or sporadic co-incidence of two neuro-endocrine tumors.
Multiple Endocrine Neoplasia type 1 (MEN1) is a rare autosomal inherited disorder with an estimated prevalence of 1–10/100,000 and is characterized by the occurrence of three primary manifestations: primary hyperparathyroidism (pHPT), duodenopancreatic neuroendocrine tumors (dpNET) and pituitary tumors (PIT) [1, 2]. According to the present clinical practice guidelines , MEN1 is diagnosed based on clinical, familial or genetic criteria. On the basis of clinical criteria, MEN1 is diagnosed if at least two out of the three primary MEN1 manifestations occur in a patient. MEN1 is diagnosed on the basis of familial criteria if a patient has a MEN1 manifestation in combination with a first degree family member with MEN1. The identification of a germline MEN1 mutation in an individual who may be asymptomatic also confirms the diagnosis of MEN1.
In 10–30 % of patients who were diagnosed with MEN1 based upon clinical criteria, no mutation was found in the MEN1 gene [4–6]. These so called ‘phenocopies’ are an upcoming diagnostic challenge. With the increased use and improvement of diagnostic techniques, the incidence and prevalence of pHPT and micro adenoma of the pituitary gland is rapidly rising. In a population-based study , the prevalence of pHPT tripled during the past two decades, increasing from 76 to 233 per 100,000 women and from 30 to 85 per 100,000 men. With an magnetic resonance imaging (MRI) scan, which is now widely available, small pituitary adenomas were found in as many as 10 % of healthy volunteers . These numbers implicate that a large number of patients might strictly meet the clinical criteria for MEN1 because of the co-incidence of pHPT and pituitary adenoma. However, it is questionable whether those patients are at risk of developing other MEN1-associated tumors and will benefit from intensive lifelong screening for MEN1-related manifestations.
Recently, research concerning other genes has been performed trying to explain the MEN1 clinical phenotype in cases of a mutation-negative MEN1 syndrome [9, 10]. In a small series of patients, a small proportion of the mutation-negative MEN1 patients appeared to have a mutation in the CDKN1B gene . These patients typically present with pituitary and parathyroid tumors. The course of the disease appeared also to be different in these patients for whom the term MEN4 was introduced .
For MEN1 patients, once the syndrome is diagnosed, the early detection of MEN1-associated tumors and subsequent interventions seem to lead to a more favorable course of the disease with a subsequent improved survival [13, 14]. Consequently, the current guidelines advise an intensive follow-up of patients with frequent laboratory and radiological investigations for all patients irrespective of age . It is, however, unclear if mutation-negative patients are at risk for developing further MEN1-related (neuro-)endocrine tumors and benefit equally from this intensive follow-up as mutation-positive patients do. To date, data on the penetrance of clinical manifestations and survival of MEN1 patients, irrespective their mutational status, are based on single- or sometimes multi-institution studies of mainly tertiary referral centers [15–20], which may have led to a selection of patients included in the studies.
Therefore, the aim of the present study was to compare the long-term clinical course of the disease in MEN1 gene mutation-positive patients with MEN1 gene mutation-negative patients from the national Dutch MEN1 cohort, including > 90 % of the MEN1 population. We studied incidence, age-related penetrance of MEN1-related manifestations, and survival in both groups of patients. Furthermore, the mutation-negative patients were invited to undergo additional genetic testing, including assessment of mutations in the CDKN1B gene.
Study design and patients
The study was performed using data from the Dutch MEN1 study group database. This longitudinal database includes > 90 % of all Dutch MEN1 patients, aged 16 years and older at the end of 2010, treated at one of the Dutch University Medical Centers (UMCs) between 1990 and 2011 . Data of all identified patients were collected according to a predefined protocol, which was based on predefined study questions from every quarter of every available year of follow-up during the period 1990–2014. The study protocol was approved by the Medical Ethical Committees of all UMCs in the Netherlands. Given the retrospective and observational data of the study, the use of these clinical data, including the results of MEN1 gene testing, were approved for the study aims and the requirement to obtain informed consent was waived. For the additional genetic analyses of CDKN1B and AIP genes in mutation-negative patients, oral and written informed consent was obtained for the testing and the use of the results in this study.
We assessed follow-up of patients with a known MEN1 gene mutation (mutation-positive) and patients with a negative MEN1 gene mutation test who had two out of the three primary MEN1 manifestations (mutation-negative).
Definitions of MEN1 manifestations
We defined pHPT as hypercalcemia combined with elevated or inappropriately non-suppressed parathyroid hormone levels in two consecutive measurements.
The reference test for the presence of pancreatic neuroendocrine tumor (NET) was the outcome of pathology examination. If pathology was not available, pancreatic NET presence was based on MRI, computed tomography (CT) or endoscopic ultrasound, which had to be confirmed at least once by consecutive imaging studies. The absence of pancreatic NET also had to be confirmed on a minimum of two subsequent imaging studies during follow-up . A duodenal NET was diagnosed with gastroduodenoscopy and, if available, by pathology. A dpNET was diagnosed according to the reference standard of pancreatic NET and duodenal NET. Thymic-NET was diagnosed based upon the results of pathology examination. Patients were considered to have a lung NET if (1) pathology examination showed lung NET or (2) radiological examination was positive for lung NET, as previously described . Gastric NET was diagnosed by gastroduodenoscopy and had to be confirmed by pathology.
The reference standard for the presence of PIT was (1) pathology or (2) radiological examination demonstrating a PIT. Details for the reference standard of pit have been described previously .
An adrenal tumor (ADR) was diagnosed based on pathology, and if pathologic examination was not available, on radiological imaging (CT or MRI) which had to be confirmed on subsequent imaging.
DNA was extracted from peripheral blood. The presence of a MEN1 mutation was determined with DNA sequencing since 1998 and with a combination of DNA sequencing and multiplex ligation-dependent probe amplification (MLPA) since 2005. MLPA (MRC-Holland, Amsterdam, The Netherlands) is used for detecting large deletions or duplications in the MEN1 gene. In addition, mutation-negative patients were invited to participate in a genetic screening program for familial NETs (including CDKN1B and AIP). The presence of a CDKN1B and AIP mutation was determined by direct sequencing. In addition, MLPA was used for AIP to detect large deletions or duplications. Sequences were analyzed with Sequencing Analysis software version 5.2 (Applied Biosystems) and compared with the reference sequences of each gene (Ensembl identifiers: MEN1 gene EST00000312049; CDKN1B gene: NM_004064.4 and AIP gene: ENST00000279146) using SeqScape software version 2.5 (Applied Biosystems). Primer sequences and PCR conditions are available on request.
The primary outcomes of the study were the age-related penetrance of the MEN1 manifestations. The secondary outcomes were the incidence of MEN1 manifestations per 1000 patient-years and the survival of patients. The primary and secondary outcomes were compared between the mutation-positive and mutation-negative patient groups.
Age-related penetrance of the primary MEN1 manifestation and other MEN1-associated tumors was estimated using the Kaplan–Meier method. Age-related penetrance was calculated for the age per manifestation, and for the age on which a first, second, and third major MEN1 manifestation was diagnosed.
Subgroup analyses for mutation-positive and mutation-negative patients was performed for the age of first, second, and third major MEN1 manifestation and the occurrence of the first other MEN1-associated tumor. In addition, a subgroup analyses was performed comparing patients in whom MEN1 was diagnosed because of the occurrence of two of the primary MEN1 manifestations (index patients) who were mutation-positive on the one hand and mutation-negative patients on the other. Index patients were not siblings of a known MEN1 family before clinical diagnosis of MEN1 and testing. Comparison of Kaplan–Meier curves was made using the Log-rank test.
Survival was compared for mutation-positive and mutation-negative patients using the Kaplan–Meier method. Cause of death was subdivided in MEN1 related and non-MEN1 related. Comparison was made using the Log-rank test. Cause and age of death was compared between mutation-positive and mutation-negative patients.
Incidence rate was calculated for the three primary MEN1 manifestations. For calculation of incidence, only tumors detected at follow-up of patients with MEN1 syndrome, i.e. after establishing the MEN1 diagnosis, were considered.
To describe clinical characteristics, the mean ± SD or median with range was calculated, depending on the normal distribution. Continuous variables were analyzed by using independent sample t-test or Mann–Whitney U test. Dichotomous variables were compared with Fisher exact test or χ2 test.
Statistical significance was set at P < 0.05 and the analyses were conducted using SPSS 20.0.
In the period 1990–2011, a total of 322 MEN1 patients were included in the database. There was a female predominance (n = 187, 58.1 %) and the patients were part of 121 different MEN1 families. At the moment of genetic testing, 100 patients were diagnosed based on clinical grounds and those patients were not siblings of a known MEN1 family. These patients represent the subgroup of index patients, 70 (70 %) of whom tested positive and 30 (30 %) tested negative for the MEN1 mutation. The other patients were all mutation-positive siblings of already known MEN1 families; 91 were pre-symptomatic at testing, and 131 patients were tested after development of the first MEN1 manifestation. The total number of MEN1-positive patients was 292 (90.7 %).
The median age of diagnosis of MEN1 was 37 years (range 8–78). In MEN1 gene mutation-negative patients, median age of diagnosis of MEN1 was 55 years (range 23–78), and was 20 years higher than the age of diagnosis of mutation-positive MEN1 patients (median age MEN1 diagnosis 35 years (range 8–78 years); P < 0.001).
In 92 % of the patients, at least one of the three main MEN1 manifestations was diagnosed. pHPT occurred in 87.0 % of patients and was diagnosed at a mean age of 36 years (SD 14 years). The youngest patient diagnosed with pHPT was 11 years old. dpNET occurred in 55.9 % and PIT in 43.8 %. The mean age at diagnosis of dpNET and PIT was 41 years (SD 15 years) and 40 years (SD 15 years), respectively. Age-related penetrance for the three main manifestations is presented in Fig. 1a–c. The prevalence of other manifestations associated with MEN1 was gastric NET in 3.7 %, lung NET in 19.3 %, thymic NET in 4.0 %, and ADR in 31.4 % of patients (Table 1). Median age and range for all manifestations are presented in Additional file 1: Table S1.
Incidence of primary MEN1 manifestations
Primary hyperparathyroidism was predominantly diagnosed before MEN1 was diagnosed. Therefore, the incidence of pHPT during follow-up was ‘only’ 144.5 per 1000 patient-years (95 % confidence interval (CI), 113.3–181.8; 73 new cases in 119 patients followed 505 patient-years). Incidence of PIT was 39.6 per 1000 patient-years (95 % CI, 31.7–48.9; 87 new cases in 230 patients followed 2195 patient-years). The incidence of dpNET was 62.3 per 1000 patient-years (95 % CI, 51.8–74.3; 124 new cases in 241 patients followed for 1990 patient-years.
The median age at which patients developed the first major manifestation was 13 years higher in MEN1 mutation-negative patients: 46.0 years (95 % CI, 39.6–52.4) compared to 33.0 years (95 % CI, 30.9–35.1) in MEN1 mutation-positive patients (P = 0.007) (Fig. 2a). Median age at developing the second major manifestation was 9 years higher in mutation-negative patients; however, the difference was not significant, 55.0 years (95 % CI, 48.3–61.7) in MEN1 mutation-negative patients versus 46.0 years (95 % CI, 43.3–48.7) in mutation-positive patients (P = 0.559) (Fig. 2b). A third main manifestation did not develop in MEN1 mutation-negative patients, compared to a total of 76 in the mutation-positive patient group, corresponding with a median age of 72 for developing the third manifestation (P < 0.001) (Fig. 2c). Finally, other MEN1-associated manifestations developed in only one patient who was MEN1 mutation-negative (ADR), while 48.3 % of mutation-positive patients developed such manifestations at a median age of 57.0 (53.5–60.5) (Fig. 2d).
Comparable results were found when the subgroup of index patients and mutation-negative patients were compared (Additional file 1: Figure S1). In this subgroup analysis, the mean age at diagnosis of the second major manifestation in mutation-positive index cases was 38.0 years (95 % CI, 35.8–40.2), which is 17 years younger compared to mutation-negative patients (P = 0.003). A third main manifestation was found in 32 mutation-positive index cases at a median age of 65 years.
After a median follow-up period from the moment of MEN1 diagnosis of 10 years (range 0–47 years), 54 patients died (16.8 %). Cause of death can be found in Additional file 1: Table S2. Among the mutation-positive MEN1 patients, 51 died (17.5 %), of whom 30 (58.8 %) due to a MEN1-related cause. The mean age of death was 60 years (SD 12 years). Among mutation-negative patients, three patients died (10.0 %) from causes not related to MEN1. Survival curves are presented in Additional file 1 (Fig. 3). Median survival in mutation-positive patients was estimated at 73.0 years (95 % CI, 69.5–76.5) compared to 87.0 years (95 % CI not available) in mutation-negative patients (P = 0.001).
Survival in mutation-positive index patients was comparable with the survival in other mutation-positive cases. Median survival in mutation-positive index cases was estimated at 72.0 years (95 % CI, 67.0–77.0; Additional file 1: Figure S2). A total of 22 mutation-positive index patients died during follow-up, 16 (72.7 %) of whom due to a MEN1-related cause (Additional file 1: Table S4).
Additional genetic results in mutation-negative patients
Full results of manifestation and additional genetic testing in MEN1 mutation-negative patients are summarized in Additional file 1: Table S3. In the 30 mutation-negative patients, no family members with MEN1 were identified. A pHPT/PIT phenotype was present in 23 patients (76.7 %), five patients had pHPT/dpNET (16.7 %) and two had PIT/dpNET (6.7 %).
In 21 of 27 patients (77.8 %) who were still alive, permission was obtained for additional genetic analysis, one patient could not give permission because of the presence of dementia. In all 21 patients, genetic testing for CDKN1B had been performed, which revealed a CDKN1B mutation in one patient. This patient, who was diagnosed with pHPT and PIT, had a mutation in the CDKN1B gene (c.295_305dup p.Gln104Argfs*19). At this location a duplication of 11 base pairs was detected in exon 1, causing a frame shift starting at codon Gln104. The new reading frame ends in a STOP codon 18 positions downstream. In 19 out of 21 patients, genetic testing for AIP was performed, which did not result in additional mutations.
In the Netherlands, MEN1 patients have an increased risk of premature death with an estimated median survival of 73 years, which is almost 10 years shorter compared with the general Dutch population. MEN1 mutation-negative patients appeared to have a far less aggressive course of disease. In mutation-negative patients, the age of the first MEN1 manifestation was higher, and a third MEN1-related manifestation hardly ever occurred. A striking result is the difference in age of death and median survival when MEN1 mutation-positive patients are compared with mutation-negative patients. The shorter life expectancy of mutation-positive MEN1 patients is in line with previous literature. The apparent differences in penetrance of MEN1 manifestations and survival between MEN1 mutation-negative and positive patients indicate that MEN1 mutation-negative patients with two out of the three main MEN1 manifestations have a different MEN1 mimicking disease. Additional testing for CDKN1B mutations in our national MEN1 cohort led to one positive, not previously described, mutation underlining the rarity of CDKN1B mutations as explanation for the MEN1 phenotype.
To minimize selection bias, age-related penetrance was analyzed in the national Dutch MEN1 study group cohort of MEN1 patients, which includes more than 90 % of the total Dutch MEN1 population . The follow-up data was collected based on pre-defined study questions and according to a standardized protocol for every quarter of every year from 1990 up to 2011. The database is considered of high quality for its high density of reliable data and long-term follow-up. To our knowledge for the first time, the age-related penetrance and age of death were compared between mutation-positive and mutation-negative patients. Diagnosis of a MEN1 manifestation was established through predefined reference standards to increase reliability. MEN1 manifestations diagnosed only on imaging had to be confirmed on consecutive examinations leading to a valid diagnosis. Further, assessment of the incidence of newly diagnosed manifestations over time is relatively new in the MEN1 research field. In this study, additional testing for mutations in the CDKN1B gene was performed and the finding of only one positive test underlines the rarity of these mutations when also tested in a national cohort.
Comparison with the other literature
The prevalence of the major MEN1-related manifestations, age-related penetrance and the survival rates are comparable with the present literature [19, 20, 25]. The previously reported percentages of mutation-negative patients vary, but our 9.3 % compares low to some earlier studies [3, 5, 6]. Moreover, in previous studies, more than 50 % of index patients without a family history of MEN1 were mutation-negative, compared to 30 % in our study [6, 26–28]. The mutation-negative patients included in our database generally underwent the recently implemented MLPA analysis, which increased the sensitivity of MEN1 gene analysis leading to a lower proportion of MEN1 mutation-negative patients. In another recent study, a comparable rate of 10 % mutation-negative patients was identified .
Previous studies have reported that mutation-negative patients are predominantly index patients without a family history of MEN1 [6, 26–28]. In our cohort all mutation-negative patients were index patients, confirming the results of previous reports. In some reports it was already suggested that patients scoring negative on both mutational testing and familial history more often have mild clinical presentation [26, 28]. We have now demonstrated that the differences in the clinical course of mutation-positive and negative patients are lasting at long-term follow-up. Index patients who scored positive at mutational testing, however, have a comparable course of the disease as patients with familial occurrence of MEN1. The differences in clinical course suggest that the mutation-negative patients may not have the MEN1 syndrome.
Recently, a new germ-line mutation in the CDKN1B gene  was discovered in mutation-negative MEN1 patients, which is now identified as MEN4. Incidence and clinical implications of MEN4 syndrome are still unknown . Mutations of the MEN1 gene and CDKN1B polymorphisms can also coincide, resulting in early development of aggressive tumors in MEN1 patients . In our cohort, permission for additional genetic analysis was obtained from 21 of 27 live patients (77.8 %). Only one CDKN1B mutation was found in all tested patients. Our findings are in accordance with the few studies published in which sporadic and familial cases of mutation-negative MEN1 patients are tested for CDKN1B [5, 30–33]. These studies also show that mutations in CDKN1B and the other genes coding CDKIs are extremely rare, and many patients who are mutation-negative and have a MEN1 like disease still have a genetically unexplained phenotype.
The CDKN1B mutation, which we found in one patient, had not been described before. The duplication of 11 base pairs causes a frame shift, resulting in a STOP codon. The mRNA produced might be targeted for non-sense mediated decay. We assume that this is a pathogenic mutation, because of the presence of an STOP codon. A number of somatic mutations in exon 1 of the CDKN1B gene are described.
Strictly spoken, we might have missed mutation-negative patients with two main MEN1-associated tumors who were not referred to one of the UMCs. However, in the Dutch healthcare system, especially patients with a lower age of diagnosis of manifestations or a more aggressive course of the disease are generally referred to one of the UMCs. Missing patients who were not referred can therefore be expected to have led to an underestimation of the differences between the MEN1 mutation-positive and -negative patients underlining the validity of the results. Finally, in The Netherlands, all genetic tests for MEN1 are performed only at the genetic laboratory of the UMC Utrecht, leading to completeness of the data. Extrapolating the clinical data from the application forms for the genetic tests that led to negative results led to the conclusion that the majority of mutation-negative patients had been included .
Nine of the 30 mutation-negative patients were not tested for CDKN1B. These missing data could lead to an underestimation of the incidence of CDKN1B mutations among the MEN1 mutation-negative patients. However, the low prevalence of CDKN1B mutations is in line with previous literature.
At the moment of diagnosis of the first manifestation, the MEN1 mutation-negative patients were not suspected to have MEN1 by the treating physician. Therefore, routine follow-up and screening as part of the MEN1 protocol started only after diagnosis of the second main manifestation. Thus, age of the second manifestation might be overestimated in the mutation-negative patients. However, the outcomes were confirmed by the results of the additional analysis in which MEN1 mutation-negative patients were compared with newly diagnosed MEN1 mutation-positive patients (index patients) who often underwent mutation analyses because of the combination of two MEN1 manifestations and also started structured follow-up after the diagnosis of MEN1.
According to our results, the age of MEN1 diagnosis and the age of the MEN1 manifestations are significantly higher in mutation-negative patients with two of the main MEN1-associated tumors. We have now demonstrated that these patients also have a more favorable clinical course, justifying the concept that these patients might not have a true MEN1 syndrome, but a MEN1-like syndrome or sporadic co-incidence of two (neuroendocrine) tumors. According to the favorable clinical course of these patients, it is questionable whether or not these patients should be intensively screened for future endocrine events according to the clinical guidelines for MEN1 patients.
Caution is warranted when encountering a mutation-negative patient who has a positive family history for MEN1 or with three MEN1-related manifestations. In our cohort, all mutation-negative patients were index cases with two main MEN1-related manifestations and a negative family history; however, previous papers have reported negative mutational testing in patients with familial occurring MEN1 [6, 26, 28]. We do expect that cases with a negative mutational testing in combination with a positive family history will become highly uncommon in the present era of highly sensitive tests such as MLPA and next generation sequencing [34, 35].
In conclusion, MEN1 is a syndrome with high life-time occurrence of pHPT, dpNET, and PIT and a considerable risk of premature death with an estimated median survival of 73 years. MEN1 mutation-positive and mutation-negative patients have a different clinical course, with mutation-negative patients developing MEN1 manifestations at a higher age and having a median survival comparable to the general population, which is 10 years longer than MEN1 mutation-positive patients. Mutations in the CDKN1B gene can be considered a rarity and do not fully explain the occurrence of MEN1 phenocopies. The apparent differences in clinical course suggests that mutation-negative patients with two out of the three main MEN1 manifestations do not have true MEN1, but another MEN1-like syndrome or sporadic co- incidence of two NETs.
- AIP :
Aryl hydrocarbon receptor interacting protein
- CDKN1B :
Cyclin-Dependent Kinase Inhibitor 1B
Duodenopancreatic neuroendocrine tumors
Multiple Endocrine Neoplasia type 1
Multiple Endocrine Neoplasia type 4
Multiplex ligation-dependent probe amplification
- MRI scan:
Magnetic resonance imaging scan
Primary hyperparathyroidism (pHPT)
University Medical Centers
- 95% CI:
95% confidence interval
Chandrasekharappa SC, Guru SC, Manickam P, Olufemi SE, Collins FS, Emmert-Buck MR, et al. Positional cloning of the gene for multiple endocrine neoplasia-type 1. Science. 1997;276:404–7.
Kouvaraki MA, Lee JE, Shapiro SE, Gagel RF, Sherman SI, Sellin RV, et al. Genotype-phenotype analysis in multiple endocrine neoplasia type 1. Arch Surg. 2002;137:641–7.
Thakker RV, Newey PJ, Walls GV, Bilezikian J, Dralle H, Ebeling PR, et al. Clinical practice guidelines for multiple endocrine neoplasia type 1 (MEN1). J Clin Endocrinol Metab. 2012;97(9):2990–3011.
Lemos MC, Thakker RV. Multiple endocrine neoplasia type 1 (MEN1): analysis of 1336 mutations reported in the first decade following identification of the gene. Hum Mutat. 2008;29:22–32.
Georgitsi M, Raitila A, Karhu A, van der Luijt RB, Aalfs CM, Sane T, et al. Germline CDKN1B/p27Kip1 mutation in multiple endocrine neoplasia. J Clin Endocrinol Metab. 2007;92:3321–5.
Cebrian A, Ruiz-Llorente S, Cascon A, Pollan M, Diez JJ, Pico A, et al. Mutational and gross deletion study of the MEN1 gene and correlation with clinical features in Spanish patients. J Med Genet. 2003;40, e72.
Yeh MW, Ituarte PH, Zhou HC, Nishimoto S, Liu IL, Harari A, et al. Incidence and prevalence of primary hyperparathyroidism in a racially mixed population. J Clin Endocrinol Metab. 2013;98:1122–9.
Hall WA, Luciano MG, Doppman JL, Patronas NJ, Oldfield EH. Pituitary magnetic resonance imaging in normal human volunteers: occult adenomas in the general population. Ann Intern Med. 1994;120:817–20.
Lindberg D, Akerstrom G, Westin G. Evaluation of CDKN2C/p18, CDKN1B/p27 and CDKN2B/p15 mRNA expression, and CpG methylation status in sporadic and MEN1-associated pancreatic endocrine tumours. Clin Endocrinol (Oxf). 2008;68:271–7.
Milne TA, Hughes CM, Lloyd R, Yang Z, Rozenblatt-Rosen O, Dou Y, et al. Menin and MLL cooperatively regulate expression of cyclin-dependent kinase inhibitors. Proc Natl Acad Sci U S A. 2005;102:749–54.
Pellegata NS, Quintanilla-Martinez L, Siggelkow H, Samson E, Bink K, Hofler H, et al. Germ-line mutations in p27Kip1 cause a multiple endocrine neoplasia syndrome in rats and humans. Proc Natl Acad Sci U S A. 2006;103:15558–63.
Thakker RV. Multiple endocrine neoplasia type 1 (MEN1) and type 4 (MEN4). Mol Cell Endocrinol. 2014;386:2–15.
Pieterman CR, Schreinemakers JM, Koppeschaar HP, Vriens MR, Rinkes IH, Zonnenberg BA, et al. Multiple endocrine neoplasia type 1 (MEN1): its manifestations and effect of genetic screening on clinical outcome. Clin Endocrinol (Oxf). 2009;70:575–81.
Lourenco Jr DM, Toledo RA, Coutinho FL, Margarido LC, Siqueira SA, dos Santos MA, et al. The impact of clinical and genetic screenings on the management of the multiple endocrine neoplasia type 1. Clinics (Sao Paulo). 2007;62:465–76.
Ferolla P, Falchetti A, Filosso P, Tomassetti P, Tamburrano G, Avenia N, et al. Thymic neuroendocrine carcinoma (carcinoid) in multiple endocrine neoplasia type 1 syndrome: the Italian series. J Clin Endocrinol Metab. 2005;90:2603–9.
Dean PG, van Heerden JA, Farley DR, Thompson GB, Grant CS, Harmsen WS, et al. Are patients with multiple endocrine neoplasia type I prone to premature death? World J Surg. 2000;24:1437–41.
Trump D, Farren B, Wooding C, Pang JT, Besser GM, Buchanan KD, et al. Clinical studies of multiple endocrine neoplasia type 1 (MEN1). QJM. 1996;89:653–69.
Schaaf L, Pickel J, Zinner K, Hering U, Hofler M, Goretzki PE, et al. Developing effective screening strategies in multiple endocrine neoplasia type 1 (MEN 1) on the basis of clinical and sequencing data of German patients with MEN 1. Exp Clin Endocrinol Diabetes. 2007;115:509–17.
Goudet P, Bonithon-Kopp C, Murat A, Ruszniewski P, Niccoli P, Menegaux F, et al. Gender-related differences in MEN1 lesion occurrence and diagnosis: a cohort study of 734 cases from the Groupe d'etude des Tumeurs Endocrines. Eur J Endocrinol. 2011;165:97–105.
Machens A, Schaaf L, Karges W, Frank-Raue K, Bartsch DK, Rothmund M, et al. Age-related penetrance of endocrine tumours in multiple endocrine neoplasia type 1 (MEN1): a multicentre study of 258 gene carriers. Clin Endocrinol (Oxf). 2007;67:613–22.
de Laat JM, Tham E, Pieterman CR, Vriens MR, Dorresteijn JA, Bots ML, et al. Predicting the risk of multiple endocrine neoplasia type 1 for patients with commonly occurring endocrine tumors. Eur J Endocrinol. 2012;167:181–7.
de Laat JM, Pieterman CR, Weijmans M, Hermus AR, Dekkers OM, de Herder WW, et al. Low accuracy of tumor markers for diagnosing pancreatic neuroendocrine tumors in multiple endocrine neoplasia type 1 patients. J Clin Endocrinol Metab. 2013;98:4143–51.
de Laat JM, Pieterman CR, van den Broek MF, Twisk JW, Hermus AR, Dekkers OM, et al. Natural Course and Survival of Neuroendocrine Tumors of Thymus and Lung in MEN1 Patients. J Clin Endocrinol Metab. 2014;99:3325–33.
de Laat JM, Dekkers OM, Pieterman CR, Kluijfhout WP, Hermus AR, Pereira AM, et al. Long-term natural course of pituitary tumors in patients with MEN1: results from the Dutch MEN1 study group (DMSG). J Clin Endocrinol Metab. 2015;100:3288–96.
Ito T, Igarashi H, Uehara H, Berna MJ, Jensen RT. Causes of death and prognostic factors in multiple endocrine neoplasia type 1: a prospective study: comparison of 106 MEN1/Zollinger-Ellison syndrome patients with 1613 literature MEN1 patients with or without pancreatic endocrine tumors. Medicine (Baltimore). 2013;92:135–81.
Hai N, Aoki N, Shimatsu A, Mori T, Kosugi S. Clinical features of multiple endocrine neoplasia type 1 (MEN1) phenocopy without germline MEN1 gene mutations: analysis of 20 Japanese sporadic cases with MEN1. Clin Endocrinol (Oxf). 2000;52:509–18.
Ellard S, Hattersley AT, Brewer CM, Vaidya B. Detection of an MEN1 gene mutation depends on clinical features and supports current referral criteria for diagnostic molecular genetic testing. Clin Endocrinol (Oxf). 2005;62:169–75.
Tham E, Grandell U, Lindgren E, Toss G, Skogseid B, Nordenskjold M. Clinical testing for mutations in the MEN1 gene in Sweden: a report on 200 unrelated cases. J Clin Endocrinol Metab. 2007;92:3389–95.
Circelli L, Ramundo V, Marotta V, Sciammarella C, Marciello F, Del PM, et al. Prognostic role of the CDNK1B V109G polymorphism in multiple endocrine neoplasia type 1. J Cell Mol Med. 2015;19(7):1735–41.
Ozawa A, Agarwal SK, Mateo CM, Burns AL, Rice TS, Kennedy PA, et al. The parathyroid/pituitary variant of multiple endocrine neoplasia type 1 usually has causes other than p27Kip1 mutations. J Clin Endocrinol Metab. 2007;92:1948–51.
Owens M, Stals K, Ellard S, Vaidya B. Germline mutations in the CDKN1B gene encoding p27 Kip1 are a rare cause of multiple endocrine neoplasia type 1. Clin Endocrinol (Oxf). 2009;70:499–500.
Igreja S, Chahal HS, Akker SA, Gueorguiev M, Popovic V, Damjanovic S, et al. Assessment of p27 (cyclin-dependent kinase inhibitor 1B) and aryl hydrocarbon receptor-interacting protein (AIP) genes in multiple endocrine neoplasia (MEN1) syndrome patients without any detectable MEN1 gene mutations. Clin Endocrinol (Oxf). 2009;70:259–64.
Agarwal SK, Mateo CM, Marx SJ. Rare germline mutations in cyclin-dependent kinase inhibitor genes in multiple endocrine neoplasia type 1 and related states. J Clin Endocrinol Metab. 2009;94:1826–34.
Giacche M, Panarotto A, Mori L, Daffini L, Tacchetti MC, Pirola I, et al. A novel menin gene deletional mutation in a little series of Italian patients affected by apparently sporadic multiple endocrine neoplasia type 1 syndrome. J Endocrinol Invest. 2012;35:124–8.
Raef H, Zou M, Baitei EY, Al-Rijjal RA, Kaya N, Al-Hamed M, et al. A novel deletion of the MEN1 gene in a large family of multiple endocrine neoplasia type 1 (MEN1) with aggressive phenotype. Clin Endocrinol (Oxf). 2011;75:791–800.
We want to thank Rumo PM Jansen for the performance of additional DNA analysis.
An unrestricted starting grant was received from Ipsen Pharmaceuticals and the Comprehensive Cancer Center, The Netherlands (IKNL).
JML: Study design, data collection, statistical analysis, interpretation of data, and drafting and final approval of the manuscript. RBL: Study design, genetic analysis, interpretation of data, and drafting and final approval of the manuscript. CRP: Design of data collection tool, data collection, and critical revision and final approval of the manuscript. MPO: Statistical analysis and drafting and final approval of the manuscript. ARH, OMD, WWH, ANH-S, MLD, PHB, BH, and MRV: Study design and critical revision and final approval of the manuscript. GDV: Study design, supervision of data collection, interpretation of data, critical revision and final approval of the manuscript.
The authors declare that they have no competing interests.
Unrestricted grant from Ipsen Pharmaceuticals, starting grant from the Comprehensive Cancer Centre the Netherlands (IKNL). Ipsen Pharmaceuticals provided an unrestricted starting grant for the database, and had no further influence on the design of the database, data acquisition, analyses, or the content of the manuscript.
Age of diagnosis of MEN1-associated manifestations. Table S2. Causes of mortality. Table S3. Clinical characteristics and results of genetic screening. Figure S1. Age-related penetrance of major manifestations and other MEN1-associated tumors compared between mutation positive index patients and mutation negative patients. Figure S2. Survival curve of MEN1 patients, comparing between mutation-positive and mutation-negative index patients. Table S4. Causes of mortality in index cases. (PDF 928 kb)
About this article
Cite this article
de Laat, J.M., van der Luijt, R.B., Pieterman, C.R.C. et al. MEN1 redefined, a clinical comparison of mutation-positive and mutation-negative patients. BMC Med 14, 182 (2016). https://doi.org/10.1186/s12916-016-0708-1