The genetic background of circadian and ultradian rhythm patterns of 17-hydroxycorticosteroids: a cross-twin study

1985 ◽  
Vol 105 (2) ◽  
pp. 247-253 ◽  
Author(s):  
A. Reinberg ◽  
Y. Touitou ◽  
A. Restoin ◽  
C. Migraine ◽  
F. Levi ◽  
...  

ABSTRACT Circadian and ultradian rhythms in urinary excretion of 17-hydroxycorticosteroids were documented individually during an 8-day span in two pairs of young male twins. Studies were performed once at the age of 6 years for dizygotic twins and twice at the ages of 4·3 and 10·3 years for monozygotic twins. Four different methods were used for time-series analyses: chronograms (raw data), best-fitting curves resulting from cosinor analyses, power spectra and correlations of time-qualified data. Estimates of rhythm parameters (prominent periods, acrophases, etc.) as well as shapes of curves were closer in mono- than in dizygotic twins. Both similarities and small differences in rhythm characteristics of monozygotic twins were detected at both ages considered. J. Endocr. (1985) 105, 247–253

2003 ◽  
Vol 31 (7) ◽  
pp. 657-662 ◽  
Author(s):  
Shahuria Enam

This paper contains a review of genetic factors in depressive affects. A large number of research findings have been reported for this purpose, the most important of these being the twin study. Monozygotic and dizygotic twins have been differentiated. It has been found that monozygotic twins have a higher concordance rate for affective illness than do dizygotic twins. Moreover, bipolar and unipolar illnesses were found in the relatives of unipolar patients only. Thus affective illness in the first degree of relatives of bipolar patients was more than 30%. Genetic transmission was also found in linkage relationship. Chromosomal studies have also been reported. Phenotypic variations have also been found to be responsible for affective illness. In conclusion, a better clinical, biochemical, and therapeutic investigation has been suggested for better understanding of genetic factors in affective illness.


2007 ◽  
Vol 148 (4) ◽  
pp. 147-153
Author(s):  
Krisztina Hagymási ◽  
Zsolt Tulassay

The majority of liver diseases, are complex. They are the results of interactions between several genes and environmental factors. Familial aggregation and higher concordance rate of monozygotic twins compared to those of dizygotic twins provide evidence for the importance of genetic factors in the pathogenesis. There are only limited data in connection with the genetic background of multifactorial liver diseases. In the future, the genetic background may permit prevention, early, accurate diagnosis, prediction of disease course, complications, prognosis, as well as treatment response.


Author(s):  
Юлия Черткова ◽  
Yuliya Chertkova ◽  
Марина Егорова ◽  
Marina Yegorova

The paper reflects one of the aspects of the research carried out within the framework of the project “Nature of variability of negative personality traits: a twin study”. The research reviews the adaptive component of negative personal traits. The sample of the study consisted of 136 members of monozygotic twins and 401 only children in their families aged 18-78. Life satisfaction was a generalized metric of psychological adaptation. It is shown that a number of negative personality traits (in particular, narcissism, authoritarianism) positively correlate with life satisfaction. The biased value of various personality traits, which can also indirectly serve as an indicator of adaptability of these psychological properties, was assessed using a semantic differential. The age-related changes in the perfect image of the self, which are associated primarily with some more attractive negative personal traits, as well as the multidirectional desired changes in personality traits in themselves and the twin (more power and conflict in themselves and less of the same in the brother/sister) also indicate that a number of negative personal traits play a positive role in psychological adaptation. It is assumed that these traits can have a compensatory function during stress, and the destructiveness of these traits can have a greater impact on people around than on themselves.


Author(s):  
Praveen Jodalli ◽  
Ganesh Panchmal ◽  
Vinej Somaraj ◽  
Shafees Koya

Abstract Aim: To assess the dentofacial characteristics of a mystery village of twins in South India. Materials and methods: A descriptive cross-sectional study was carried out among of 22 twin pairs (10 monozygotic twins and 12 dizygotic twins). The evaluation was done in terms of height, weight, dentofacial profile, and occlusion status based on anthropometric, photographic, and dental cast analysis. Results: Data obtained upon analysis of anthropometric measurements, photographic data, and dental cast evaluation revealed a set of characteristics peculiar to the twins of this unique village. Conclusion: Twin studies are a fascinating method of research because of their ability to correctly isolate a characteristic and determine its impact, especially in terms of dentofacial characteristics. Clinical significance: Twin research design involving the comparison of variables among monozygotic (identical) and dizygotic (fraternal) twins is a method by which researchers quantify and classify the contribution of genes and other extraneous factors influencing heredity on the dentofacial complex and dentition.


2001 ◽  
Vol 86 (11) ◽  
pp. 5479-5484 ◽  
Author(s):  
Richard G. IJzerman ◽  
Coen D. A. Stehouwer ◽  
Mirjam M. van Weissenbruch ◽  
Eco J. de Geus ◽  
Dorret I. Boomsma

Recent studies have demonstrated an association between low weight at birth and an atherogenic lipid profile in later life. To examine the influences of intrauterine and genetic factors, we investigated 53 dizygotic and 61 monozygotic adolescent twin pairs. Regression analysis demonstrated that low birth weight was associated with high levels of total cholesterol, low-density lipoprotein (LDL) cholesterol and apolipoprotein B (−0.17 mmol/liter per kg, P = 0.07; −0.18 mmol/liter per kg, P = 0.04; and− 0.07 g/liter per kg, P = 0.02, respectively) and with low levels of high-density lipoprotein (HDL) cholesterol (+0.04 mmol/liter per kg, P = 0.1), after adjustment for age, sex, and body mass index. Intrapair differences in birth weight were significantly associated with differences in total cholesterol, LDL cholesterol, and apolipoprotein B in dizygotic twins after adjustment for differences in current body mass index (−0.49 mmol/liter per kg, P = 0.02; −0.51 mmol/liter per kg, P = 0.01; and −0.10 g/liter per kg, P = 0.04, respectively), demonstrating that the larger the difference in birth weight, the higher these risk factors in the twin with the lower birth weight, compared with the cotwin with the higher birth weight. In monozygotic twins, however, the associations between intrapair differences in birth weight and differences in total cholesterol, LDL cholesterol, and apolipoprotein B were in the opposite direction (+0.32 mmol/liter per kg, P = 0.03; +0.23 mmol/liter per kg, P = 0.08; and +0.06 g/liter per kg, P = 0.04, respectively). The association between intrapair differences in birth weight and differences in HDL cholesterol was not significant in dizygotic twins (+0.04 mmol/liter per kg, P = 0.6) and of borderline significance in monozygotic twins (+0.11 mmol/liter per kg, P = 0.05). These data suggest that genetic factors account for the association of low birth weight with high levels of total cholesterol, LDL cholesterol, and apolipoprotein B, whereas intrauterine factors possibly play a role in the association between birth weight and HDL cholesterol.


1976 ◽  
Vol 10 (2) ◽  
pp. 157-162
Author(s):  
Takao Hattori

The EEGs of twenty-five pairs of twins, one or both of whom were mentally retarded, were studied. The concordance rate for mental retardation in monozygotic twins was higher than that in dizygotic twins. The vast majority of cases of mental retardation were considered to be caused by genotype but some exogenous causes were observed in discordant monozygotic twins. Paroxysmal discharges in the EEG especially those of centrencephalic type were suspected to be bio-electrical expressions of a transmissible cerebral susceptibility which may easily lead to intellectual deterioration by brain damage or epilepsy.


2005 ◽  
Vol 8 (3) ◽  
pp. 198-200 ◽  
Author(s):  
Shiao Hui M. Liew ◽  
Hanno Elsner ◽  
Tim D. Spector ◽  
Christopher J. Hammond

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