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. 2018 May 21;31(3):284–288. doi: 10.1080/08998280.2018.1463784

Table 1.

Clinical presentation of the 30 patients who met initial criteria for familial chylomicronemia syndromea

Variable Result
Male 22 (73%)
Age at pancreatitis onsetb (years) 37.3 ± 10.1
Age at analysis (years) 40.2 ± 10.1
Body mass index (kg/m2) 32.5 ± 4.5
Hispanic 14 (47%)
Family history of high triglycerides 7 (23%)
Xanthoma 1 (3%)
Diabetes mellitus 27 (90%)
Insulin-dependent diabetes mellitus 21 (70%)
Diabetic ketoacidosis 6 (20%)
Cholecystectomy 13 (43%)
Spleen vein thrombosisc 6 (29%)
Hepatic steatosisd 20 (87%)
Alcohol abuse 6 (20%)
Smoker (current) 9 (30%)
Smoker (former) 15 (50%)
Laboratory values  
 Peak triglyceride in study period (mg/dL) 2864.3 ± 1254.5
 Lowest triglyceride in study period (mg/dL) 244 [170, 334]
 High-density lipoprotein (mg/dL) 30.3 ± 10.7
 Low-density lipoprotein (mg/dL) 80.9 ± 43.9
 Total cholesterol (mg/dL) 213 [164, 286]
 Triglyceride/total cholesterol (at peak triglyceride) 7.4 [5.0, 8.7]
 Triglyceride/total cholesterol (most recent) 3.3 [1.8, 4.8]
 Hemoglobin (mg/dL) 14.1 ± 1.8
Medications  
 Statin 24 (80%)
 Maximum statin 7 (23%)
 Fibrate 28 (93%)
 Omega-3 16 (53%)
a

Twenty-four were clinically adjudicated as having familial chylomicronemia syndrome.

b

This was calculated with the first documented date in a patient's chart; these were not back-dated, even if a patient had pancreatitis as a child.

c

n = 21.

d

n = 23.