La tunisie Medicale - 2012 ; Vol 90 ( n°03 ) : 259 - 262
[ 8676 times seen ]
Summary
Background: Inborn errors of metabolism are neglected in developing countries because they are not as common as infectious and nutritional disorders. In Tunisia, no information is available on the incidence and epidemiological features of these inherited metabolic diseases.
Aims: To precise the profile of aminoacidopathies other than phenylketonuria and organic acidurias and to estimate their incidences in Tunisia.
Methods: Between 1987 and 2009, our laboratory received 13171 requests for analysis of patients with symptoms suggestive of inborn errors of metabolism. For these cases, ion exchange chromatography of free amino acids was performed on amino acids analyser. Urinary organic acids profiles were determined by gas chromatography-mass spectrometry.
Results: Abnormal cases were 370 (2.8%), divided into 212 cases of aminoacidopathies (57.3%) and 158 cases of organic acidurias (42.7%). The most frequent aminoacidopathies, were maple syrup disease (32.5%), tyrosinemia type I (28.8%) and nonketotic hyperglycinemia (16%). Methylmalonic aciduria (33.5%), propionic aciduria (18.4%) and 2-hyrdoxy glutaric aciduria (10.8%) were the most frequent organic acidurias. The incidences were calculated using the Hardy-Weinberg formula and were estimated at 1/13716 for maple syrup disease, 1/14804 for tyrosinemia type I, 1/16144 for methylmalonic aciduria and 1/23176 for propionic aciduria.
Conclusion: Aminoacidopathies and organic acidurias turned out to be highly frequent in Tunisia, mainly because of a high rate of consanguinity. We believe that they are underestimated. To improve their diagnosis, it is necessary to have available sophisticated equipment which would allow early treatment of patients.
Key - Words
Article
Inborn errors of metabolism (IEM) seem to be common in the Middle East and North Africa, where high consanguinity rates still prevail due to frequents marriages between close relatives [1-3]. Diagnosis of these diseases on the basis of clinical symptoms followed by biological confirmation constitutes a reliable approach for both providing early diagnostic and therapeutic services. Among these IEM, worldwide, aminoacidopathies (AAP) and organic acidurias (OAP) have a relatively high incidence [4-6]. IEM are not given great interest in developing countries because they are not as common as infectious and nutritional disorders, and consequently are generally under-diagnosed. However, they may contribute significantly to morbidity and mortality. Hence a reliable and cost effective screening for early diagnosis is vitally important [7]. In Tunisia, no information is available on the incidence and epidemiological features of these diseases.
This retrospective study reports, the different AAP other than Phenylketonuria (PKU) and OAP, diagnosed in the metabolic division of the laboratory of biochemistry of the Rabta Hospital during a period of 23 years (1987-2009 inclusive). We estimate also the incidences of the most prevalent disorders of them in Tunisia. PKU is the most common AAP in Tunisia and has been explored in other studies [8- 9].

MATERIAL AND METHODS


Patients

In Biochemistry Laboratory of Rabta Hospital, 13171 patients with symptoms suggestive of IEM were investigated between 1987 and 2009. The cases were from different regions of Tunisia and therefore constitute a random representative sample from the entire country population. Data can thus be considered reliable estimate of the actual disease incidence. Main original hospital departments of these patients were paediatrics (75.4%), neonatology (10%) and neurology (4.6%).

Methods

Samples
The samples included random urine, fasting venous blood (collected into heparin-containing tube) and cerebrospinal fluid whenever the diagnosis of nonketotic hyperglycinemia (NKH) was suspected. These samples were complemented with information sheets where the following variables were recorded: age, gender, geographical origin, consanguinity, previous family history of IEM, the main clinical symptoms and current therapy.

Initial testing
Screening included blood and urine one-dimensional amino acid thin layer chromatography in n-butanol: acetone: acetic acid: water (35:35:10:20) [10]. Cephalic spinal fluid amino acids were also studied in patients with suspected NKH. Specialized testing In the case of abnormal result of the amino acid thin layer chromatography, ion exchange chromatography on amino acids analyser (Beckman 6300) was performed for the quantification of aminoacids. Urinary organic acids profiles were determined by gas chromatography-mass spectrometry (Hewlett Packard 5890/HP 5972).

Statistical analysis


Collected data on confirmed patients (AAP and OAP cases) were analyzed using Epi-Info software.

RESULTS

During 23 years of selective screening, 370 AAP and OAP cases were diagnosed corresponding to 22 IEM, giving 2.8 % of total of 13171 patients screened. These IEM were divided into respectively, 212 AAP cases (57.3 %) grouping 9 different enzyme deficiencies and 158 OAP cases (42.7 %) with 13 different types of abnormalities. The three most common disorders of amino acids metabolism were maple syrup urine disease (MSUD), tyrosinemia type I and NKH. Methylmalonic aciduria, propionic aciduria and 2-hyrdoxy glutaric aciduria were the most frequent OAP disorders (tables 1 and 2). Sex ratio was 1.36 for male/female. Consanguinity accounted for 86.7 % and the presence of previous similar disorders in the family was identified in 67.5 % of cases. When data is considered according to geographical origin, no hot spot location for these disorders could be singled out within the country, but for MSUD 97% of cases originate from west central Tunisia and for NKH 71% of patients were from central Tunisia.

Table 1 : Number and respective frequencies of different types of aminoacidopathies and age at diagnosis
Table 2 : Number and respective frequencies of different types of organic acidurias and age at diagnosis

Age at diagnosis varied between 1 day and 49 years with a mean age of 1 year and 9 months. NKH is the AAP whose clinical symptoms were the earliest followed by MSUD, sulfite oxidase and xanthine oxidase deficiency and tyrosinemia type I. For other AAP, onset of clinical symptoms was later in our patients. Concerning OAP, onset of clinical symptoms was very heterogeneous. Despite this variability, we remark early onset of clinical signs during propionic, methylmalonic and pyroglutamic aciduria (tables 1 and 2).
The main clinical symptoms likely related to clinical disease state in new born and infants patients were, hypotonia (73.6%), metabolic acidosis (65.2%), seizures (61%), failure to feed (59.5%), respiratory difficulties (58.4%), ketosis (57.3%), coma (54.8%), persistent vomiting (53.8%), hepatomegaly (47.5%), mental retardation (47%), delay in motor development (43%) and abnormal movements (36.5%).
Using Hardy-Weinberg formula [E= M/aN + f ÃM/aN; E, estimated incidence; M: pathological cases; a: period of study (23 years: 1987-2009 inclusive); N: total of births per year during the period of study; f: coefficient of consanguinity (0.0129)] [11], the diseases incidences were estimated for AAP and OAP as one per 4514 births (1/4514). Table 3 shows the calculated incidences for the most frequent AAP and OAP.

Table 3 : Calculated incidences of the frequent aminoacidopathies other than phenylketonuria and organic acidurias.


DISSCUSION

A retrospective study of inherited metabolic diseases during 23 years in Tunisia showed that AAP were more frequent (1/4464) than AOP (1/5570). This study has been conducted on patients with a high rate of consanguinity (86%) and high rate of firstcousin marriages (56%). In addition, we notice a high frequency of similar disorders or unexplained deaths among the families of patients (67.5%). High consanguinity is common in the Middle East and North Africa, which increased the occurrence of IEM [7]. Indeed, a study of IEM in an Omani population of the Arabian Peninsula [1] found that the parental consanguinity was twice as frequent in the study patients as in the general population. Other studies from Riyadh, Saudi Arabia and Kuwait indicate that some diseases are confined to specific families and Tribal groups [12-16]. In contrast, in other studies in Italy, British Columbia, Brazil and West Midlands, patients with IEM had a low rate of consanguinity [4, 17-19].
In this study, we did not find geographic areas at higher risk of IEM, with the notable exception of west central Tunisia where MSUD (97% of cases) and NKH (72% of patients) showed a clear regional clustering. These results are similar to those in the Mexican study in which MSUD has been found more frequent in Hispanic population [20].
Age at diagnosis was very variable between different metabolic diseases. Acute diseases (such as NKH, MSUD, methylmalonic and propionic aciduria) were characterized by a sudden onset of deterioration of vital functions (like respiratory and neurological distress). motivating parents regardless of their level of consciousness to consult early. However, for other chronic pathologies (such as homocystinuria, cystinuria and 3- ‚-Ketothiolase deficiency) characterized by a gradual onset and progressive installation of clinical symptoms (such as mental retardation and delay in motor development), age at diagnosis was late because the consultation depends on the degree of awareness of parents and their socio economic conditions.
More than half of all diagnosed patients corresponded to amino acid disorders other than PKU. It is possible that AAP were often diagnosed due to the simplicity and low-cost of the detection techniques required, such as chemical screening tests and amino acid chromatography. Following PKU, MSUD was the most frequent AAP; it is interesting that an even higher frequency has been found in Saudi Arabia [13] and in Mexico [20]. Because Spain was an Islamic country for 800 years, it is tempting to speculate whether some of the MSUD mutations in the Spanishspeaking populations are of Near Eastern origin [20].
Regarding OAP, methylmalonic aciduria was the most prevalent disorder in this study and also in other studies performed in Saudi Arabia [13], Mexico [20], Italy [17] and China [21].
Some factors need to be considered when comparing these results with those of other studies. The number of cases in Tunisia is under diagnosed because, on the one hand, the patients not identified in the acute phase die quickly and on the other hand, our Laboratory is the only one specialised in the diagnosis of these diseases which creates difficulties for biological exploration of patients living far; in addition, the screening is selective and no systematic national screening programmes were done. The diagnosis is delayed for the majority of patients, because of poor socio economic conditions of some patients in isolated areas which prevent the parents to consult early.

CONCLUSION

In total, AAP and OAP seem to be highly frequent in Tunisia, because of a high rate of consanguinity. It is necessary to make available sophisticated equipment, to improve the diagnosis of AAP and AOP as well as other disorders; this is essential to early diagnosis and effective management and emergency treatments of patients with suspected IEM.

Aknowledgments

The authors would like to thank all clinicians of hospital departments in Tunisia for their collaboration, in particular Paediatrics, Neonatology, Neurology, Neuropaediatrics, Genetics, Dermatology and Ophthalmology. They would like to thank also technicians of the biochemistry laboratory: Dalinda Bouhadra, Salma Ben Ayed, Saloua Skhiri Mustpha Mzoughi and Aida Abidli, for their technical assistance.
Reference
  1. Joshi SN, Hashim J, Venugopalan P. Pattern of inborn errors of metabolism in an Omani population of Arabian Peninsula. Ann Trop Paediatr 2002; 22:93-96.
  2. Teebi A, El-Shanti H. Consanguinity: implications for practice, research and policy. Lancet 2006; 367:970-71.
  3. Bittles AH. When cousins marry: a review of consanguinity in the Middle East. Prespect Hum Biol 1995; 1:71-83.
  4. Sanderson S, Green A, Preece MA, Burton H. The incidence of inherited metabolic disorders in the West Mildlands, UK. Arch Dis Child 2006; 91:896-99.
  5. Wasant P, Svasti J, Srisomsap C, Limmongkolkul S. Inherited metabolic disorders in Thailand. J Med Assoc Thai 2002; 85:S700-S9.
  6. Widhalm K. 25 years Austrian screening program for inborn errors of metabolism at the Vienna University. Wien Klin Wochenschr 1992; 104:510-3.
  7. Sadallah AA, Rached MS. Newborn screening: Experiences in the Middle East and North Africa. J Inherit Metab Dis 2007; 30:482- 9.
  8. Khemir S, Tebib N, Nasrallah F et al. Phenylketonuria in Tunisian institutions for the mentally handicapped. Arch Dis Child. 2009; 94:647-8.
  9. Khemir S, Elasmi M, Sanhaji H et al. Phenylketonuria is still a major cause of mental retardation in Tunisia despite the possibility of treatment. Clin Neurol Neurosurg 2011; 113: 727- 30.
  10. Hans JB, Marinus D, Johannis PK et al. Disturbances of amino acid metabolism: clinical chemistry and diagnosis. USA: Urban & Schwarzenberg Baltimore-Munich; 1981:450
  11. Monastiri K, Khairi H, Snoussi N, Ghannem H, Hajfredj A. Biométrie du nouveau né dans le Sahel Tunisien. Ann Pediatr 1994; 41:578-83.
  12. Moammar H, Cheriyan G, Mathew R, Al-Sannaa N. Incidence and patterns of inborn errors of metabolism in the Eastern Province of Saudi Arabia, 1983-2008. Ann Saudi Med. 2010; 30:271-7.
  13. Ozand PT, Devol EB, Gascon GG. Neurometabolic diseases at a national referral center: Five years experience at the King Faisal specialist hospital and research center. J Child Neurol 1992; S7:4- 11.
  14. Rashed M, Ozand PT, al Aqeel A, Gascon GG. Experience of King Faisal specialist hospital and research center with Saudi organic acid disorders. Brain Dev 1994; S16:1-6.
  15. Ozand PT. Diagnosis of inborn errors of metabolism by tandem mass spectrometry. Ann Saudi Med 1998; 18:234-8.
  16. Abdel-Hamid M, Tisocki K, Sharaf L, Ramadan D. Development, validation and application of tandem mass spectrometry for screening of inborn metabolic disorders in Kuwaiti Infants. Med Princ Pract 2007; 16:215-21.
  17. Carlo Dionisi V, Risso C, Burlina Ab et al. Inborn errors of metabolism in the Italian pediatric population: a retrospective survey. J Pediatr 2002; 3:321-7.
  18. Applegarth DA, Toone JR, Lowry RB. Incidence of inborn errors of metabolism in British Columbia, 1969-1996. Pediatrics 2000; 105:e10.
  19. Simoni RE, Oliveira SPH, Grassiano DM, et al. Screening for inborn errors of metabolism in high-risk children from Rio de Janeiro, Brazil. Early Hum Dev 1998; 50:305-11.
  20. Velázquez A, Vela-Amieva M, Cicerón-Arellano I et al. Diagnosis of inborn errors of metabolism. Arch Med Res 2000; 31:145-50.
  21. Han LS, Ye J, Qiu WJ et al. Diagnosis of inborn errors of metabolism using tandem mass spectrometry and gas chromatography mass spectrometry. Zhonghua Yi Xue Za Zhi 2008; 88:2122-6.
Login
E-mail :
Password :
Remember Me Forgot password? Sign UP
Archives
2021
January
February
March
April
May
June
July
August
September
October
November
December
Keywords most used
treatment Child diagnosis surgery prognosis Tunisia Children Crohn’s disease Breast cancer screening Cancer epidemiology Ulcerative colitis obesity prevention
Newsletter
Sign up to receive our newsletter
E-mail :
Stay in Touch
Join Us! !