On the combined effects of normobaric hypoxia and bed rest upon bone and mineral metabolism: Results from the PlanHab study
2016 (English)In: Bone, ISSN 8756-3282, E-ISSN 1873-2763, Vol. 91, 130-138 p.Article in journal (Refereed) Published
Bone losses are common as a consequence of unloading and also in patients with chronic obstructive pulmonary disease (COPD). Although hypoxia has been implicated as an important factor to drive bone loss, its interaction with unloading remains unresolved. The objective therefore was to assess whether human bone loss caused by unloading could be aggravated by chronic hypoxia. In a cross-over designed study, 14 healthy young men underwent 21-day interventions of bed rest in normoxia (NBR), bed rest in hypoxia (HBR), and hypoxic ambulatory confinement (HAmb). Hypoxic conditions were equivalent to 4000 m altitude. Bone metabolism (NTX, P1NP, sclerostin, DKK1) and phospho-calcic homeostasis (calcium and phosphate serum levels and urinary excretion, PTH) were assessed from regular blood samples and 24-hour urine collections, and tibia and femur bone mineral content was assessed by peripheral quantitative computed tomography (pQCT). Urinary NTX excretion increased (P<0.001) to a similar extent in NBR and HBR (P = 0.69) and P1NP serum levels decreased (P = 0.0035) with likewise no difference between NBR and HBR (P = 0.88). Serum total calcium was increased during bed rest by 0.059 (day D05, SE 0.05 mM) to 0.091 mM (day D21, P < 0.001), with no additional effect by hypoxia during bed rest (P = 0.199). HAmb led, at least temporally, to increased total serum calcium, to reduced serum phosphate, and to reduced phosphate and calcium excretion. In conclusion, hypoxia did not aggravate bed rest-induced bone resorption, but led to changes in phospho-calcic homeostasis likely caused by hyperventilation. Whether hyperventilation could have mitigated the effects of hypoxia in this study remains to be established.
Place, publisher, year, edition, pages
Elsevier, 2016. Vol. 91, 130-138 p.
Immobilization, Respiration, Human physiology, Sclerostin, DKK1
IdentifiersURN: urn:nbn:se:kth:diva-193159DOI: 10.1016/j.bone.2016.07.013ISI: 000382431600014PubMedID: 27443510ScopusID: 2-s2.0-84979645563OAI: oai:DiVA.org:kth-193159DiVA: diva2:1037531
QC 201610172016-10-172016-09-302016-10-17Bibliographically approved