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Dergi Kimliği

Online ISSN (İngilizce)
1305-3124

Basılı ISSN (Türkçe)
1300-5251

Online ISSN (Türkçe)
1305-3132

Kuruluş
1993

Editör
Cihat Şen

Yardımcı Editörler
Murat Yayla, Oluş Api

The determınatıon of zygosıty

Louis Keith, Mahantesh Karoshi

Künye

The determınatıon of zygosıty. Perinatoloji Dergisi 2005;13(2):s29-31

Yazar Bilgileri

Louis Keith1,
Mahantesh Karoshi2

  1. Department of Obstetrics and Gynecology,The Feinberg School of Medicine Northwestern University- Chicago, Illinois US
  2. The Center for Study of Multiple Birth,North Middlesex University Hospital- London GB
Yazışma Adresi

Louis Keith, Department of Obstetrics and Gynecology,The Feinberg School of Medicine Northwestern University- Chicago, Illinois US,

Yayın Geçmişi

Yayınlanma Tarihi: 01 Nisan 2005

Çıkar Çakışması

Çıkar çakışması bulunmadığı belirtilmiştir.

Monozygotic (MZ) twins occur when one oocyte is fertilized by one spermatizoon and at some later timedivides to form two embryos. The causes of this split are uncertain. Dizygotic (DZ) twins occur when twooocytes are fertilized by two spermatozoon. The frequency of MZ twinning probably is constant throughout theworld, whereas DZ twinning is racially mediated with the highest rate occurring in Africans and the lowest in Asians. When unlike sex twins are born, no question exists regarding their zygosity. They are by definition DZ. In contrast, when like-sexed twins are born, the question of zygosity arises. Unless chorionicity has been demonstrated accurately in the antenatal period and correctly interpreted at the time of delivery, it is possible toerr in zygosity assignment based on placentation and membranes. In this error, it is commonly assumed thatlike-sexed twins are DZ, because it is determined that they are dichorionic (DC) at birth. The genesis of thiserror is the widespread recognition that like-sexed DC twins (with fused or separate placental discs) may be DZor MZ (approximately 25% are MZ). The term "identical" is commonly used as a shortcut for MZ, but this is a serious misnomer. Rarely if ever are MZ twins "identical" in their phenotypic appearance even if they carry the same genetic patrimony.

WHEN TO TEST FOR ZYGOSIT
The optimal time to determine zygosity is at delivery. The obstetrician can do the assessment easily, eitheralone or in consultation with the pathologist. The benefits of such an assessment include: first, the ability tostate with certainty that MC twins are MZ; and second, the institution of formal zygosity testing, using placental tissue, in all like-sexed DC twins, recognizing that 25% of such twins are MZ and the remainder DZ.AVAILABLE METHODS OF

ZYGOSITY DETERMINATION
Historical: In 1874, the French mathematician, Bertillon, assumed that the sex of each zygote of a pair of DZ twins would be determined independently, postulating that the number of DZ pairs was equal to twice the number of unlike-sex pairs, with the remainder of the like-sexed pairs presumably MZ. Restated in 1902 by Weinberg, this concept was criticized almost from its inception and is still subject to intense negative interpretation, as its usefulness is purely confined to statistical samples.

Physical Characteristics Assessment: Over the years, the following characteristics have been studied: biometric parameters, skeletal structures, skin, hair and dermatoglyphics, ocular and orbital anatomy, nasal anddental characteristics, and specularity (mirrored or reversed asymmetry). Many such physical characteristics arepoorly developed in newborns, and, later in life, comparisons are often not sufficiently robust to determine adefinitive diagnosis of zygosity. Additional characteristics used, albeit with varying degrees of efficacy, include: ear forms, patterns of ridging on the tongue and dental eruption patterns, as well as tooth morphology.Fingerprints are never completely identical, neither are the patterns in the iris of the eye. Indeed, the probabilityof two different irises agreeing by chance in more than 70% of their phase sequences is one in seven billion.

COMMONLY USED METHOD
SBlood Groups: A commonly used and relatively inexpensive method of zygosity determination is the use ofblood groups and human leukocyte antigens (HLA). Zygosity can be determined from blood by studying common population variants known as polymorphisms. These include the common blood groups, HLA types,serum proteins, enzyme polymorphisms and, most recently, DNA variations. Using the ABO blood groups as an example, if the father of the twins is blood group AB and the mother isgroup O, the offspring may be either group A or group B. If one twin is group A and the other is group B, the pair is clearly DZ. If both are A or B, however, zygosity is unproven. The process can then be repeated for many other sets of polymorphisms, with the intent of establishing differences (diagnostic of DZ) or, alternatively, a high statistical probability of MZ on the basis of failing to detect differences. The higher thestatistical probability desired, the more difficult it is to achieve.

DNA:
DNA is undoubtedly the most sophisticated form of zygosity detection using blood and other bodily tissues as the substrate. It is commonly characterized as ‘DNA fingerprinting’. Although many authoritiesdescribe it as being most accurate, it can also be most confusing because, as of this writing, there is no goldstandard for the analytic procedure. DNA testing analyzes genes rather than their protein products. As such,several genetic loci are tested simultaneously, and a pattern unique to the individual is quickly determined.Using this technology, MZ twins share identical genomic patterns in some studies. The likelihood that a DZpair would also exhibit superimposable patterns is exceedingly low (3x10-14th). The major problem in DNA analysis for determination of zygosity relates to the existence of small-scale mutations. This is the process by which DNA changes in specific zones, e.g. point mutations, deletions andinsertions, trinucleotide repeat sequences, and tandem repeat sequences

INCREASING POSTNATAL DISCORDANCET
he phenomenon of increasing post-natal discordance supports the concept that MZ twins are not truly "identical". A number of post-zygotic phenomena begin at birth and affect the respective genotypes of MZpairs. The extent to which these changes are visible depends to a great degree on the method used to analyzethe DNA components. One method uses a number of microsatellite probes, also called variable number of tandem repeat markers (VNTR). The other uses restriction fragment polymorphism (RFLP). The formermethodology examines DNA under a high-power microscope, as it were, whereas the latter examines segments of DNA at "lesser magnification" and provides a "broad brush stroke" diagnosis of monozygosity by failing to pick up the inevitable smaller, post-zygotic mutational differences that are now thought to be presentin most, if not all, MZ twin pairs. Case Study: The senior author (LK) and his identical twin brother (Donald Keith) exemplify some of the difficulties in accurate zygosity determination. Both are male and there were two placental discs and membranous sacs at the time of their birth in 1935. They were classified as DZ on the basis of the placentationalone by no less an authority than Dr. Irving Stein of Stein-Leventhal fame. Their childhood phenotypicappearances were remarkably similar, so much so that the diagnosis of DZ became questionable in their minds.At the age of 41, they were examined by Professors Luigi Gedda, Robert Deron and Walter Nance whorequested blood samples and finger print analyses. Based on the results of these examinations, they weredeclared to be MZ with the probability of 99.6%. When DNA analyses first became available, a mouthwash sample of both twins was obtained for an absorptionspectrum. Based on a difference in one DNA zone where multiple repeat sequences were present they werereclassified as DZ by Dr. Andreas Busjahn of the Franz Volhard Clinic and the Max Delbruck Center for Molecular Medicine of the Humboldt University in Berlin. When RFLP technology was used shortly thereafterin two different reference laboratories (Fiona Bamforth in Canada, and Catherine Derom in Belgium), theywere once again classified as MZ. Further Considerations: Because of the uncertainties just described, the use of combinations of tests has beenproposed. A logical supplement to any of the standard tests is a self-or parent administered questionnaire. Thisconcept is not new, but its use in combination with other tests is more recent. Accuracy of most reported testsis 90% or more.

IMPLICATIONS FOR CLINICAL PRACTICE

The following implications for practice derive from the recognition of the complex nature of zygosity testing,its long and continuing evolution and recent advances in ultrasound and molecular genetics.
1.All MC twins are MZ, but they may be discordant for genetic disease, malformations, etc.
2.Unlike sexed twins are DZ.
3.Not all like-sexed DC twins are DZ.
4.Not all like-sexed twins conceived using ART are DZ.
5.Not all twins who are discordant for genetic disease, chromosome constitution or a major malformation are DZ.
6.All like sex twins have the right to know their zygosity.
7.Correct terminology, i.e., MZ/DZ, should always be used rather than misleading and inaccurate terms suchas identical/fraternal.
Anahtar Kelimeler

Kaynaklar
1.Blickstein I and Keith L, Multiple Pregnancy; Epidemiology, Gestation and Perinatal Outcome (Second Edition) 2005, Taylor andFrancis, London, Chapter 94, pp776-784.