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Published on: May 31, 2016
Familial aggregation of medial arterial calcification in Pima Indians with and without diabetes
K M Narayan1, D J Pettitt, R L Hanson
1Diabetes and Arthritis Epidemiology Section, National Institute of Diabetes and Digestive and Kidney Diseases, Phoenix AZ 85014, USA. vna@cu.nih.gov
Insights
Medial arterial calcification (MAC) shows familial aggregation, indicating genetic factors may play a role. Parental MAC increases offspring risk, independent of diabetes, suggesting distinct underlying causes.
Area of Science:
- Cardiovascular research
- Genetics
- Metabolic disorders
Background:
- Medial arterial calcification (MAC) is a poorly understood condition linked to age, sex, diabetes, and its complications.
- Familial aggregation studies are crucial for understanding the genetic contribution to MAC.
Purpose of the Study:
- To investigate the familial aggregation of medial arterial calcification (MAC).
- To determine if familial MAC aggregation is independent of diabetes.
Main Methods:
- Radiological examination of MAC in the feet of 3,339 offspring from 1,256 Pima Indian nuclear families.
- Multiple logistic regression analyses to assess the association between parental and offspring MAC, controlling for diabetes.
Main Results:
- Offspring with one parent affected by MAC had 3.3 times the odds of MAC; those with both parents affected had 8.1 times the odds.
- Parental MAC significantly predicted offspring MAC (P < 0.001), independent of parental age and diabetes.
- Parental diabetes did not significantly predict offspring MAC when parental MAC was accounted for (P = 0.36).
Conclusions:
- Parental MAC increases offspring MAC risk, independent of age, sex, and diabetes status.
- Findings suggest distinct genetic or familial factors contribute to MAC compared to diabetes.
- Further research into the genetic basis of MAC is warranted.
Objective:
Little is known about medial arterial calcification (MAC) other than its association with age, sex, diabetes, and diabetes complications. Familial aggregation of this disorder was studied to determine the importance of potential genetic factors and to assess whether such familial aggregation was independent of that of diabetes.
Research Design And Methods:
Members of 1,256 Pima Indian nuclear families with 3,339 offspring were examined radiologically for MAC of the feet. Multiple logistic regression analyses were used to compare the presence of the disorder in a parent with the presence of MAC in an offspring and to determine whether familial aggregation of MAC was independent of parental diabetes.
Results:
Controlled for age, sex, diabetes, serum cholesterol, and blood pressure, offspring of one parent with MAC had 3.3 (95% CI 1.5-7.6) times the odds of MAC as did offspring of parents without MAC, and offspring with both parents affected had an even higher risk (odds ratio, 8.1; 95% CI 3.4-18.8). Controlled for offspring age and sex and for parental age and diabetes, parental MAC was associated with the disorder in offspring (P < 0.001), but the effect of parental diabetes on MAC in the offspring was not significant when controlled for parental MAC (P = 0.36). Furthermore, offspring of nondiabetic parents with MAC, controlled for age, sex, diabetes, and diabetes duration, had 1.7 (95% CI 0.9-3.1) times the odds of MAC than did offspring of diabetic parents with MAC.
Conclusions:
Independent of parental age and diabetes and offspring age, sex, diabetes, and diabetes complications, parental MAC confers an increased risk of MAC in offspring. These findings suggest that the factors responsible for the familial clustering of MAC may be different from those for diabetes.
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