Vitamin-D Status and Mineral Metabolism in Two Ethnic Populations with Sarcoidosis. Issue 5 (April 2016)
- Record Type:
- Journal Article
- Title:
- Vitamin-D Status and Mineral Metabolism in Two Ethnic Populations with Sarcoidosis. Issue 5 (April 2016)
- Main Title:
- Vitamin-D Status and Mineral Metabolism in Two Ethnic Populations with Sarcoidosis
- Authors:
- Capolongo, Giovanna
Xu, Li Hao Richie
Accardo, Mariasofia
Sanduzzi, Alessandro
Stanziola, Anna Agnese
Colao, Annamaria
Agostini, Carlo
Zacchia, Miriam
Capasso, Giovambattista
Adams-Huet, Beverley
Moe, Orson W
Maalouf, Naim M
Sakhaee, Khashayar
Hsia, Connie C W - Abstract:
- Vitamin-D insufficiency and sarcoidosis are more common and severe in African Americans (AA) than Caucasians. In sarcoidosis, substrate-dependent extrarenal 1, 25-dihydroxyvitamin-D (1, 25-(OH)2 D) production is thought to contribute to hypercalciuria and hypercalcemia, and vitamin-D repletion is often avoided. However, the anti-inflammatory properties of vitamin-D may also be beneficial. We prospectively examined serum vitamin-D levels, calcium balance, and the effects of vitamin-D repletion in 86 AA and Caucasian patients with biopsy-proven active sarcoidosis from the USA (US) and Italy (IT) in university-affiliated outpatient clinics. Clinical features, pulmonary function, and calciotropic hormones were measured. 16 patients with vitamin-D deficiency and normal serum ionized calcium (Ca 2+ ) were treated with oral ergocalciferol (50, 000 IU/week) for 12 weeks. Baseline mineral parameters were similar in US (93% AA) and IT (95% Caucasian) patients irrespective of glucocorticoid treatment. Pulmonary dysfunction was less pronounced in IT patients. Nephrolithiasis (in 11% US, 17% IT patients) was associated with higher urinary calcium excretion. Vitamin-D deficiency was not more prevalent in patients compared to the respective general populations. As serum 25-hydroxyvitamin-D (25-OHD) rose postrepletion, serum 1, 25-(OH)2 D, γ-globulins, and the previously elevated angiotensin converting enzyme (ACE) levels declined. Asymptomatic reversible increases in Ca 2+ or urinaryVitamin-D insufficiency and sarcoidosis are more common and severe in African Americans (AA) than Caucasians. In sarcoidosis, substrate-dependent extrarenal 1, 25-dihydroxyvitamin-D (1, 25-(OH)2 D) production is thought to contribute to hypercalciuria and hypercalcemia, and vitamin-D repletion is often avoided. However, the anti-inflammatory properties of vitamin-D may also be beneficial. We prospectively examined serum vitamin-D levels, calcium balance, and the effects of vitamin-D repletion in 86 AA and Caucasian patients with biopsy-proven active sarcoidosis from the USA (US) and Italy (IT) in university-affiliated outpatient clinics. Clinical features, pulmonary function, and calciotropic hormones were measured. 16 patients with vitamin-D deficiency and normal serum ionized calcium (Ca 2+ ) were treated with oral ergocalciferol (50, 000 IU/week) for 12 weeks. Baseline mineral parameters were similar in US (93% AA) and IT (95% Caucasian) patients irrespective of glucocorticoid treatment. Pulmonary dysfunction was less pronounced in IT patients. Nephrolithiasis (in 11% US, 17% IT patients) was associated with higher urinary calcium excretion. Vitamin-D deficiency was not more prevalent in patients compared to the respective general populations. As serum 25-hydroxyvitamin-D (25-OHD) rose postrepletion, serum 1, 25-(OH)2 D, γ-globulins, and the previously elevated angiotensin converting enzyme (ACE) levels declined. Asymptomatic reversible increases in Ca 2+ or urinary calcium/creatinine (Ca/Cr) developed in three patients during repletion. In conclusion, Caucasian and AA patients show similar calcium and vitamin D profiles. The higher prevalence of hypercalciuria and nephrolithiasis in sarcoidosis is unrelated to endogenous vitamin-D levels. Vitamin-D repletion in sarcoidosis is generally safe, although calcium balance should be monitored. A hypothesis that 25-OHD repletion suppresses granulomatous immune activity is provided. … (more)
- Is Part Of:
- Journal of investigative medicine. Volume 64:Issue 5(2016)
- Journal:
- Journal of investigative medicine
- Issue:
- Volume 64:Issue 5(2016)
- Issue Display:
- Volume 64, Issue 5 (2016)
- Year:
- 2016
- Volume:
- 64
- Issue:
- 5
- Issue Sort Value:
- 2016-0064-0005-0000
- Page Start:
- 1025
- Page End:
- 1034
- Publication Date:
- 2016-04
- Subjects:
- Clinical medicine -- Periodicals
Medicine -- Research -- Periodicals
Medicine
Research -- United States
Clinical medicine
Medicine -- Research
Periodicals
616.075 - Journal URLs:
- http://journals.lww.com/jinvestigativemed/pages/default.aspx ↗
http://jim.bmj.com/ ↗
https://journals.sagepub.com/home/IMJ ↗
http://journals.lww.com ↗ - DOI:
- 10.1136/jim-2016-000101 ↗
- Languages:
- English
- ISSNs:
- 1081-5589
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5008.010000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 24845.xml